A General and Practical Approach for the Synthesis of 1,2,4‐Trioxanes Catalyzed by Silica‐Ferric Chloride

An efficient and practical method has been developed for the facile synthesis of 1,2,4‐trioxanes by the condensation of β‐hydroperoxy alcohols and carbonyl compounds in the presence of a catalytic amount of silica‐supported ferric chloride (FeCl3/SiO2) at room temperature. The method has the benefit...

Full description

Saved in:
Bibliographic Details
Published inAdvanced synthesis & catalysis Vol. 359; no. 20; pp. 3618 - 3625
Main Authors Zhang, Mo, Han, Yi, Niu, Jia‐Liang, Zhang, Zhan‐Hui
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 25.10.2017
Wiley Subscription Services, Inc
Subjects
Online AccessGet full text

Cover

Loading…
Abstract An efficient and practical method has been developed for the facile synthesis of 1,2,4‐trioxanes by the condensation of β‐hydroperoxy alcohols and carbonyl compounds in the presence of a catalytic amount of silica‐supported ferric chloride (FeCl3/SiO2) at room temperature. The method has the benefits of operational simplicity, high yields and potential large‐scale application. Moreover, the catalyst can be readily recovered by simple filtration and reused up to five times while almost maintaining its catalytic activity.
AbstractList An efficient and practical method has been developed for the facile synthesis of 1,2,4‐trioxanes by the condensation of β‐hydroperoxy alcohols and carbonyl compounds in the presence of a catalytic amount of silica‐supported ferric chloride (FeCl3/SiO2) at room temperature. The method has the benefits of operational simplicity, high yields and potential large‐scale application. Moreover, the catalyst can be readily recovered by simple filtration and reused up to five times while almost maintaining its catalytic activity.
An efficient and practical method has been developed for the facile synthesis of 1,2,4-trioxanes by the condensation of beta-hydroperoxy alcohols and carbonyl compounds in the presence of a catalytic amount of silica-supported ferric chloride (FeCl3/SiO2) at room temperature. The method has the benefits of operational simplicity, high yields and potential large-scale application. Moreover, the catalyst can be readily recovered by simple filtration and reused up to five times while almost maintaining its catalytic activity.
An efficient and practical method has been developed for the facile synthesis of 1,2,4‐trioxanes by the condensation of β‐hydroperoxy alcohols and carbonyl compounds in the presence of a catalytic amount of silica‐supported ferric chloride (FeCl 3 /SiO 2 ) at room temperature. The method has the benefits of operational simplicity, high yields and potential large‐scale application. Moreover, the catalyst can be readily recovered by simple filtration and reused up to five times while almost maintaining its catalytic activity. magnified image
Author Han, Yi
Zhang, Mo
Niu, Jia‐Liang
Zhang, Zhan‐Hui
Author_xml – sequence: 1
  givenname: Mo
  surname: Zhang
  fullname: Zhang, Mo
  organization: Hebei Normal University
– sequence: 2
  givenname: Yi
  surname: Han
  fullname: Han, Yi
  organization: Hebei Normal University
– sequence: 3
  givenname: Jia‐Liang
  surname: Niu
  fullname: Niu, Jia‐Liang
  organization: Hebei Normal University
– sequence: 4
  givenname: Zhan‐Hui
  surname: Zhang
  fullname: Zhang, Zhan‐Hui
  email: zhanhui@mail.nankai.edu.cn
  organization: Hebei Normal University
BookMark eNqNkcFq3DAQhkVIINkk15wFPXa9lbyyZB8Xt0kLgQY2OZuxNGYVHGkreWncUx-hz5gnicIuGwiU5DQj9H8z8_NPyKHzDgm54GzGGcu_gIl6ljOuGJOKH5ATLnmRCS6rw31fsGMyifGeJVmp1Al5WNArdBigp-AMvQmgB6vTa7FeBw96RTsf6LBCuhxdKtFG6jvKp_lUPP39dxusfwSHkdYwQD_-QUPbkS5tn4ak_0sMwWpar3ofrMEzctRBH_F8V0_J3eW32_p7dv3z6ke9uM70vBA8K7XRFUouTVtoqaQApowpkOWqhVy0gieHgG0phZadEqrSeQtGJ3tlVwGfn5JP27nJw68NxqG595vg0sqGV4VIznPGkurzVvUbW99FbdFpbNbBPkAYG8aY4HOp5jJ1eZHU5cfVtR1gsN7VfuOGhM62qA4-xoDdHuOsecmuecmu2WeXAPEG0LuBQwDb_x-rdifaHsd3ljSLr8v6lX0Gu7Cvhw
CitedBy_id crossref_primary_10_1016_j_tet_2021_132379
crossref_primary_10_1039_D0NJ01301C
crossref_primary_10_1080_10426507_2018_1542395
crossref_primary_10_1007_s00706_017_2092_8
crossref_primary_10_1055_a_1643_3057
crossref_primary_10_1002_ejoc_202100343
crossref_primary_10_1016_j_bioorg_2023_107043
crossref_primary_10_1039_C8GC02611D
crossref_primary_10_1002_aoc_6667
crossref_primary_10_1007_s11164_022_04660_6
crossref_primary_10_1021_acsomega_2c01321
crossref_primary_10_1002_adsc_201900827
crossref_primary_10_2174_0113852728261733231006094620
crossref_primary_10_1002_aoc_5172
crossref_primary_10_1021_jacs_1c02249
crossref_primary_10_1002_aoc_6064
crossref_primary_10_1016_j_molliq_2019_01_065
crossref_primary_10_1016_j_cclet_2019_05_063
crossref_primary_10_1002_slct_201702326
crossref_primary_10_1007_s11164_021_04566_9
crossref_primary_10_1002_chem_201904555
crossref_primary_10_1002_adsc_202100858
crossref_primary_10_1002_ange_201807485
crossref_primary_10_1016_j_bmcl_2024_129801
crossref_primary_10_1002_aoc_5921
crossref_primary_10_1021_jacs_2c00406
crossref_primary_10_1002_anie_201807485
crossref_primary_10_1002_adsc_201900994
crossref_primary_10_1016_j_tet_2020_131059
crossref_primary_10_1039_D0GC03400B
crossref_primary_10_1021_acscombsci_9b00124
Cites_doi 10.1016/j.catcom.2016.09.028
10.1039/c3nj01368e
10.1039/C5GC00381D
10.1002/ejoc.201500919
10.1016/j.cclet.2015.01.035
10.1021/jm9002523
10.1016/j.tetlet.2016.12.002
10.1016/0040-4039(91)80487-Q
10.1139/v99-001
10.1021/jm400004u
10.1002/anie.200701397
10.1016/j.catcom.2006.02.026
10.1021/acssuschemeng.7b01102
10.1021/acs.joc.6b02091
10.1016/j.tet.2014.02.017
10.1002/adsc.201600357
10.1021/acs.joc.5b00533
10.1016/j.mcat.2016.12.001
10.1016/j.bmcl.2005.07.013
10.1246/cl.140624
10.1021/jm0610043
10.1055/s-0030-1261225
10.1007/s00706-009-0204-9
10.1080/00397910802412842
10.1016/S1872-2067(15)60829-4
10.1002/cctc.201402415
10.1021/ol0492142
10.1016/j.catcom.2016.02.004
10.1002/adsc.201500335
10.1007/s00706-014-1275-9
10.1002/adsc.201600565
10.1002/hlca.19930760804
10.3987/COM-97-S51
10.1016/j.tet.2013.06.049
10.1002/cplu.201600611
10.1039/c3ob27239g
10.1016/j.bmc.2004.08.042
10.1021/acssuschemeng.5b01183
10.1021/jm100678p
10.1002/adsc.201600759
10.1002/adsc.201100561
10.3762/bjoc.12.162
10.1002/hlca.19970800813
10.1002/cmdc.201402553
10.1021/jm301323k
10.1021/ml300188t
10.1016/j.apcata.2014.06.006
10.1080/00304948.2012.697708
10.1002/chem.201300076
10.1002/adsc.201600577
10.1055/s-0035-1561599
10.2174/1385272820666161020150646
10.1039/c2ob25376c
10.1016/j.bmcl.2010.06.045
10.1002/adsc.201300551
10.1002/ejoc.201500326
10.1016/j.ccr.2015.01.001
10.1039/C6RA19579B
10.1351/pac200577061059
10.1016/j.tetlet.2016.08.099
10.1016/j.bmcl.2007.05.055
10.2174/157017806775789903
10.1021/cr500425u
10.1021/ol026916n
10.1002/adsc.201600503
10.1002/ange.200701397
10.1016/j.bmcl.2004.11.043
10.1080/00397911.2016.1167910
10.1055/s-2005-872103
10.1039/c5gc00381d
10.1055/s-0032-1317958
10.1055/s-0028-1083147
10.1039/c6ra19579b
ContentType Journal Article
Copyright 2017 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim
2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
Copyright_xml – notice: 2017 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim
– notice: 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
DBID AAYXX
CITATION
17B
1KM
1KN
BLEPL
DTL
EGQ
GYRTJ
7U5
8FD
L7M
DOI 10.1002/adsc.201700671
DatabaseName CrossRef
Web of Knowledge
Index Chemicus
Current Chemical Reactions
Web of Science Core Collection
Science Citation Index Expanded
Web of Science Primary (SCIE, SSCI & AHCI)
Web of Science - Science Citation Index Expanded - 2017
Solid State and Superconductivity Abstracts
Technology Research Database
Advanced Technologies Database with Aerospace
DatabaseTitle CrossRef
Web of Science
Technology Research Database
Advanced Technologies Database with Aerospace
Solid State and Superconductivity Abstracts
DatabaseTitleList
Web of Science
CrossRef
Technology Research Database
Database_xml – sequence: 1
  dbid: 1KN
  name: Current Chemical Reactions
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/woscc/search-with-editions?editions=WOS.CCR
  sourceTypes:
    Enrichment Source
    Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1615-4169
EndPage 3625
ExternalDocumentID 000413673600025
10_1002_adsc_201700671
ADSC201700671
Genre article
GrantInformation_xml – fundername: National Natural Science Foundation of China
  funderid: 21272053
– fundername: Nature Science Foundation of Hebei Province
  funderid: B2015205182
– fundername: Nature Science Foundation of Hebei Province; Natural Science Foundation of Hebei Province
  grantid: B2015205182
– fundername: National Natural Science Foundation of China; National Natural Science Foundation of China (NSFC)
  grantid: 21272053
GroupedDBID -~X
05W
0R~
1L6
1OC
23M
33P
3SF
3WU
4.4
4ZD
50Y
52U
52V
5GY
5VS
66C
6P2
8-0
8-1
8UM
A00
AAESR
AAEVG
AAHHS
AAIHA
AANLZ
AAONW
AASGY
AAXRX
AAYCA
AAZKR
ABCUV
ABDBF
ABIJN
ABJNI
ABLJU
ABQWH
ABRJW
ABXGK
ACAHQ
ACCFJ
ACCZN
ACGFS
ACGOF
ACMXC
ACNCT
ACPOU
ACUHS
ACXBN
ACXQS
ADBBV
ADBTR
ADEOM
ADIZJ
ADKYN
ADMGS
ADOZA
ADXAS
ADZMN
ADZOD
AEEZP
AEIGN
AEIMD
AENEX
AEQDE
AEUQT
AEUYR
AFBPY
AFFPM
AFGKR
AFPWT
AFWVQ
AFZJQ
AHBTC
AIACR
AITYG
AIURR
AIWBW
AJBDE
ALMA_UNASSIGNED_HOLDINGS
ALUQN
ALVPJ
AMBMR
AMYDB
ATUGU
AZVAB
BDRZF
BFHJK
BHBCM
BMXJE
BNHUX
BOGZA
BRXPI
CS3
DCZOG
DPXWK
DR2
DRFUL
DRMAN
DRSTM
EBS
EJD
F5P
FUBAC
G-S
GNP
HBH
HGLYW
HHY
HHZ
HZ~
IX1
JPC
KBYEO
KQQ
LATKE
LAW
LEEKS
LITHE
LOXES
LUTES
LYRES
MEWTI
MRFUL
MRMAN
MRSTM
MSFUL
MSMAN
MSSTM
MXFUL
MXMAN
MXSTM
MY~
NNB
O66
O9-
OIG
P2P
P2W
P4E
QRW
R.K
RJQFR
ROL
RWI
RX1
RYL
SUPJJ
TUS
V2E
W99
WBKPD
WH7
WIH
WIJ
WIK
WJL
WOHZO
WXSBR
WYJ
XPP
XV2
~S-
AAMNL
AAYXX
AEYWJ
AGHNM
CITATION
17B
1KM
1KN
1OB
AAMMB
AEFGJ
AGXDD
AIDQK
AIDYY
BLEPL
DTL
GROUPED_WOS_SCIENCE_CITATION_INDEX_EXPANDED
GROUPED_WOS_WEB_OF_SCIENCE
7U5
8FD
L7M
ID FETCH-LOGICAL-c3541-8cdc9e616db5c6764a07dd5e027ba24b41067aeb864c6f7479c2badc1508f9a13
IEDL.DBID DR2
ISICitedReferencesCount 31
ISICitedReferencesURI https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000413673600025
ISSN 1615-4150
IngestDate Fri Jul 25 05:04:15 EDT 2025
Wed Aug 06 03:42:02 EDT 2025
Fri Aug 29 16:09:51 EDT 2025
Thu Apr 24 22:53:05 EDT 2025
Tue Jul 01 04:09:45 EDT 2025
Wed Jan 22 16:27:20 EST 2025
IsPeerReviewed true
IsScholarly true
Issue 20
Keywords CONVENIENT SYNTHESIS
1,2,4-trioxanes
ONE-POT SYNTHESIS
MAGNETICALLY SEPARABLE CATALYST
PROMOTED ONE-POT
carbonyl compounds
beta-hydroperoxy alcohols
silica-supported iron(III) chloride
SUPPORTED MOLYBDENUM
SPIRO 1,2,4-TRIOXANES
DIASTEREOSELECTIVE FORMATION
4-COMPONENT SYNTHESIS
RECYCLABLE CATALYST
ANTIMALARIAL 1,2,4-TRIOXANES
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
LinkModel DirectLink
LogoURL https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg
MergedId FETCHMERGED-LOGICAL-c3541-8cdc9e616db5c6764a07dd5e027ba24b41067aeb864c6f7479c2badc1508f9a13
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
PQID 1954877200
PQPubID 2045202
PageCount 8
ParticipantIDs proquest_journals_1954877200
webofscience_primary_000413673600025CitationCount
crossref_primary_10_1002_adsc_201700671
wiley_primary_10_1002_adsc_201700671_ADSC201700671
crossref_citationtrail_10_1002_adsc_201700671
webofscience_primary_000413673600025
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate October 25, 2017
PublicationDateYYYYMMDD 2017-10-25
PublicationDate_xml – month: 10
  year: 2017
  text: October 25, 2017
  day: 25
PublicationDecade 2010
PublicationPlace WEINHEIM
PublicationPlace_xml – name: WEINHEIM
– name: Heidelberg
PublicationTitle Advanced synthesis & catalysis
PublicationTitleAbbrev ADV SYNTH CATAL
PublicationYear 2017
Publisher Wiley
Wiley Subscription Services, Inc
Publisher_xml – name: Wiley
– name: Wiley Subscription Services, Inc
References 1997; 80
2017; 5
2010; 53
2015; 36
2014; 70
2013; 4
2013; 69
2017; 82
2013; 24
2015; 146
2017; 88
1997; 46
2004; 6
2015; 80
2012; 55
2017; 433
2012; 10
2016; 78
2013; 19
2010; 20
2009; 52
2013; 11
2013; 56
1993; 76
2013; 355
2016; 358
2016; 81
2014; 482
2014; 6
2005; 77
2016; 46
2007; 17
2015; 17
2009; 21
2011
1991; 32
2015; 288
2017; 21
2015; 10
2006; 7
2008
2002; 4
2006; 3
2005
2007; 50
2016; 57
2016; 12
2014; 43
2016; 4
2015; 26
2016; 6
2012; 354
2015; 115
2017; 58
2015; 357
2004; 12
2014; 38
1999; 77
2015
2009; 140
2007 2007; 119 46
2005; 15
2016; 27
2012; 44
2009; 39
e_1_2_6_51_1
e_1_2_6_53_2
e_1_2_6_74_2
e_1_2_6_32_1
e_1_2_6_30_1
e_1_2_6_72_1
e_1_2_6_19_1
e_1_2_6_13_2
e_1_2_6_34_2
e_1_2_6_59_2
e_1_2_6_11_2
e_1_2_6_17_1
e_1_2_6_38_2
e_1_2_6_55_2
e_1_2_6_76_2
e_1_2_6_15_1
e_1_2_6_57_2
e_1_2_6_78_2
e_1_2_6_62_1
e_1_2_6_64_1
e_1_2_6_81_1
e_1_2_6_20_1
e_1_2_6_41_2
e_1_2_6_60_2
Ravi M. (e_1_2_6_29_2) 2013; 24
e_1_2_6_7_2
e_1_2_6_9_3
e_1_2_6_9_2
e_1_2_6_3_2
e_1_2_6_5_2
e_1_2_6_24_2
e_1_2_6_47_2
e_1_2_6_49_2
e_1_2_6_28_2
e_1_2_6_43_2
e_1_2_6_66_1
e_1_2_6_26_2
e_1_2_6_45_2
e_1_2_6_68_1
e_1_2_6_50_2
e_1_2_6_73_2
e_1_2_6_52_2
e_1_2_6_75_2
e_1_2_6_31_1
e_1_2_6_71_2
e_1_2_6_12_2
e_1_2_6_35_2
e_1_2_6_58_2
e_1_2_6_10_2
e_1_2_6_33_2
e_1_2_6_54_2
e_1_2_6_77_2
e_1_2_6_18_1
Bartoschek A. (e_1_2_6_36_2) 2005
e_1_2_6_39_1
e_1_2_6_14_2
e_1_2_6_37_2
e_1_2_6_56_2
e_1_2_6_79_2
e_1_2_6_16_1
e_1_2_6_63_1
e_1_2_6_42_2
e_1_2_6_65_1
e_1_2_6_21_1
e_1_2_6_80_2
e_1_2_6_40_2
e_1_2_6_61_1
e_1_2_6_8_2
e_1_2_6_4_2
Kumar L. (e_1_2_6_22_2) 2009; 21
e_1_2_6_6_1
Liu Y. H. (e_1_2_6_70_2) 2008
e_1_2_6_25_1
e_1_2_6_23_2
e_1_2_6_48_2
e_1_2_6_2_1
e_1_2_6_27_2
e_1_2_6_44_2
e_1_2_6_67_1
e_1_2_6_69_1
e_1_2_6_46_2
Gawande, MB (WOS:000352252900006) 2015; 288
Liu, YH (WOS:000300448400024) 2012; 354
Pandit, RP (WOS:000390408200010) 2016; 358
Singh, C (WOS:000243889100013) 2007; 50
Mir, BA (WOS:000390407300017) 2016; 358
Griesbeck, AG (WOS:000226935700020) 2005; 15
Maurya, R (WOS:000315182000009) 2013; 4
Sharma, RK (WOS:000371755400060) 2016; 4
Li, BL (WOS:000322098000010) 2013; 69
Kadam, RG (WOS:000398034000019) 2017; 82
Singh, C (WOS:000231936700016) 2005; 15
An, YS (WOS:000347161300017) 2015; 146
Zhou, SH (WOS:000400562600013) 2017; 433
Ravi, M (WOS:000314697700008) 2013; 24
Habibi, D (WOS:000352678400020) 2015; 36
Kalhor, S (WOS:000357224900023) 2015; 26
Singh, C (WOS:000279866300036) 2010; 20
Zhang, M (WOS:000373418700006) 2016; 78
JEFFORD, CW (WOS:A1993MN64900003) 1993; 76
Mischne, MP (WOS:000079823200010) 1999; 77
Yao, N (WOS:000394169000011) 2017; 21
Murakami, R (WOS:000375004700012) 2016; 27
Griesbeck, A. G. (000413673600025.13) 2007; 119
Wang, XF (WOS:000317032200031) 2013; 56
Chari, MA (WOS:000241320000010) 2006; 7
Singh, C (WOS:000248462300001) 2007; 17
Bauer, I (WOS:000354906800005) 2015; 115
Zhang, M (WOS:000405139100063) 2017; 5
Klapotke, TM (WOS:000362747900013) 2015; 2015
Singh, C (WOS:000225050500002) 2004; 12
Bartoschek, A (WOS:000231847000026) 2005
Estevao, MS (WOS:000392896200008) 2017; 58
Griesbeck, AG (WOS:000236167900019) 2006; 3
(000413673600025.1) 2007; 46
O'Neill, PM (WOS:000223581900005) 2004; 6
Sawama, Y (WOS:000390264700002) 2016; 358
Tindall, DJ (WOS:000382969500008) 2016; 358
Kumar, M (WOS:000362527100014) 2015; 357
Zhang, ZH (WOS:000272376400012) 2009; 140
Donatoni, MC (WOS:000335873500003) 2014; 70
Zhang, M (WOS:000389330700014) 2016; 6
Griesbeck, AG (WOS:000358085100011) 2015; 2015
Jefford, CW (WOS:000071175600012) 1997; 80
JEFFORD, CW (WOS:A1991GU56900027) 1991; 32
Singh, C (WOS:000312227300030) 2012; 55
Liu, YH (WOS:000262859200002) 2009; 39
Brautigam, M (WOS:000351773300007) 2015; 10
Jefford, CW (WOS:000071491900064) 1997; 46
Liu, YH (WOS:000260777300018) 2008
Li, BL (WOS:000336821000038) 2014; 38
Bharate, SB (WOS:000305191000020) 2012; 10
Neto, JSS (WOS:000390408200009) 2016; 358
Sharma, RK (WOS:000355925900002) 2015; 17
Ghosh, P (WOS:000377815800004) 2016; 46
Kumar, L (WOS:000264759200030) 2009; 21
Zhang, YK (WOS:000307059200002) 2012; 44
Griesbeck, AG (WOS:000295158200031) 2011
Lu, J (WOS:000342795000017) 2014; 6
Zhang, M (WOS:000389117500010) 2017; 88
Griesbeck, AG (WOS:000230007100012) 2005; 77
Singh, C (WOS:000283703000008) 2010; 53
Li, PH (WOS:000328149300029) 2013; 355
Ramachandran, G (WOS:000343272600036) 2014; 43
Naidu, PS (WOS:000356845800040) 2015; 80
Terent'ev, AO (WOS:000316803900010) 2013; 11
Zhao, XN (WOS:000340306500031) 2014; 482
Griesbeck, AG (WOS:000266296200033) 2009; 52
Hao, HD (WOS:000319417500038) 2013; 19
Yaremenko, IA (WOS:000381258800001) 2016; 12
Samanta, S (WOS:000386187500063) 2016; 81
Griesbeck, AG (WOS:000179430600003) 2002; 4
Majumdar, S (WOS:000384873300021) 2016; 57
References_xml – start-page: 3314
  year: 2008
  end-page: 3318
  publication-title: Synthesis
– volume: 354
  start-page: 441
  year: 2012
  end-page: 447
  publication-title: Adv. Synth. Catal.
– volume: 358
  start-page: 3586
  year: 2016
  end-page: 3599
  publication-title: Adv. Synth. Catal.
– volume: 43
  start-page: 1631
  year: 2014
  end-page: 1633
  publication-title: Chem. Lett.
– volume: 433
  start-page: 91
  year: 2017
  end-page: 99
  publication-title: Mol. Catal.
– volume: 4
  start-page: 1123
  year: 2016
  end-page: 1130
  publication-title: ACS Sustainable Chem. Eng.
– volume: 77
  start-page: 237
  year: 1999
  end-page: 242
  publication-title: Can. J. Chem.
– volume: 80
  start-page: 6381
  year: 2015
  end-page: 6390
  publication-title: J. Org. Chem.
– volume: 12
  start-page: 5745
  year: 2004
  end-page: 5752
  publication-title: Bioorg. Med. Chem.
– volume: 38
  start-page: 2435
  year: 2014
  end-page: 2442
  publication-title: New J. Chem.
– volume: 88
  start-page: 39
  year: 2017
  end-page: 44
  publication-title: Catal. Commun.
– volume: 5
  start-page: 6175
  year: 2017
  end-page: 6182
  publication-title: ACS Sustainable Chem. Eng.
– volume: 44
  start-page: 340
  year: 2012
  end-page: 374
  publication-title: Org. Prep. Proced. Int.
– volume: 17
  start-page: 4097
  year: 2007
  end-page: 4101
  publication-title: Bioorg. Med. Chem. Lett.
– volume: 27
  start-page: 1187
  year: 2016
  end-page: 1192
  publication-title: Synlett
– volume: 355
  start-page: 2952
  year: 2013
  end-page: 2959
  publication-title: Adv. Synth. Catal.
– volume: 6
  start-page: 106160
  year: 2016
  end-page: 106170
  publication-title: RSC Adv.
– volume: 26
  start-page: 735
  year: 2015
  end-page: 738
  publication-title: Chin. Chem. Lett.
– volume: 82
  start-page: 467
  year: 2017
  end-page: 473
  publication-title: ChemPlusChem
– volume: 52
  start-page: 3420
  year: 2009
  end-page: 3423
  publication-title: J. Med. Chem.
– volume: 80
  start-page: 2440
  year: 1997
  end-page: 2455
  publication-title: Helv. Chim. Acta
– volume: 70
  start-page: 3231
  year: 2014
  end-page: 323
  publication-title: Tetrahedron
– volume: 24
  start-page: 173
  year: 2013
  end-page: 176
  publication-title: Synlett
– volume: 358
  start-page: 3471
  year: 2016
  end-page: 3476
  publication-title: Adv. Synth. Catal.
– volume: 53
  start-page: 7587
  year: 2010
  end-page: 7598
  publication-title: J. Med. Chem.
– volume: 358
  start-page: 3683
  year: 2016
  end-page: 3687
  publication-title: Adv. Synth. Catal.
– volume: 358
  start-page: 2398
  year: 2016
  end-page: 2403
  publication-title: Adv. Synth. Catal.
– volume: 46
  start-page: 685
  year: 2016
  end-page: 691
  publication-title: Synth. Commun.
– volume: 55
  start-page: 10662
  year: 2012
  end-page: 10673
  publication-title: J. Med. Chem.
– volume: 32
  start-page: 7243
  year: 1991
  end-page: 7246
  publication-title: Tetrahedron Lett.
– volume: 119 46
  start-page: 9040 8883
  year: 2007 2007
  end-page: 9043 8886
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– volume: 146
  start-page: 165
  year: 2015
  end-page: 172
  publication-title: Monatsh. Chem.
– volume: 39
  start-page: 580
  year: 2009
  end-page: 589
  publication-title: Synth. Commun.
– volume: 482
  start-page: 258
  year: 2014
  end-page: 265
  publication-title: Appl. Catal. A: Gen.
– volume: 78
  start-page: 26
  year: 2016
  end-page: 32
  publication-title: Catal. Commun.
– volume: 21
  start-page: 3540
  year: 2009
  end-page: 3546
  publication-title: Asian J. Chem.
– volume: 6
  start-page: 2854
  year: 2014
  end-page: 2859
  publication-title: ChemCatChem
– volume: 357
  start-page: 2862
  year: 2015
  end-page: 286
  publication-title: Adv. Synth. Catal.
– volume: 58
  start-page: 302
  year: 2017
  end-page: 304
  publication-title: Tetrahedron Lett.
– volume: 77
  start-page: 1059
  year: 2005
  end-page: 1074
  publication-title: Pure Appl. Chem.
– volume: 76
  start-page: 2775
  year: 1993
  end-page: 2788
  publication-title: Helv. Chim. Acta
– volume: 69
  start-page: 7011
  year: 2013
  end-page: 7018
  publication-title: Tetrahedron
– start-page: 2433
  year: 2005
  end-page: 2444
  publication-title: Synthesis
– volume: 358
  start-page: 3572
  year: 2016
  end-page: 3585
  publication-title: Adv. Synth. Catal.
– volume: 15
  start-page: 4484
  year: 2005
  end-page: 4487
  publication-title: Bioorg. Med. Chem. Lett.
– volume: 140
  start-page: 1481
  year: 2009
  end-page: 1483
  publication-title: Monatsh. Chem.
– volume: 7
  start-page: 787
  year: 2006
  end-page: 790
  publication-title: Catal. Commun.
– volume: 17
  start-page: 3207
  year: 2015
  end-page: 3230
  publication-title: Green Chem.
– volume: 57
  start-page: 4595
  year: 2016
  end-page: 4598
  publication-title: Tetrahedron Lett.
– volume: 4
  start-page: 4193
  year: 2002
  end-page: 4195
  publication-title: Org. Lett.
– volume: 50
  start-page: 521
  year: 2007
  end-page: 527
  publication-title: J. Med. Chem.
– volume: 10
  start-page: 5143
  year: 2012
  end-page: 5150
  publication-title: Org. Biomol. Chem.
– start-page: 6237
  year: 2015
  end-page: 6242
  publication-title: Eur. J. Org. Chem.
– volume: 4
  start-page: 165
  year: 2013
  end-page: 169
  publication-title: ACS Med. Chem. Lett.
– volume: 115
  start-page: 3170
  year: 2015
  end-page: 3387
  publication-title: Chem. Rev.
– volume: 36
  start-page: 620
  year: 2015
  end-page: 625
  publication-title: Chin. J. Catal.
– volume: 11
  start-page: 2613
  year: 2013
  end-page: 2623
  publication-title: Org. Biomol. Chem.
– volume: 3
  start-page: 247
  year: 2006
  end-page: 249
  publication-title: Lett. Org. Chem.
– volume: 288
  start-page: 118
  year: 2015
  end-page: 143
  publication-title: Coord. Chem. Rev.
– volume: 20
  start-page: 4459
  year: 2010
  end-page: 4463
  publication-title: Bioorg. Med. Chem. Lett.
– volume: 56
  start-page: 2547
  year: 2013
  end-page: 2255
  publication-title: J. Med. Chem.
– volume: 21
  start-page: 368
  year: 2017
  end-page: 377
  publication-title: Curr. Org. Chem.
– volume: 10
  start-page: 629
  year: 2015
  end-page: 639
  publication-title: ChemMedChem
– start-page: 2430
  year: 2011
  end-page: 2432
  publication-title: Synlett
– volume: 15
  start-page: 595
  year: 2005
  end-page: 597
  publication-title: Bioorg. Med. Chem. Lett.
– volume: 81
  start-page: 10088
  year: 2016
  end-page: 10093
  publication-title: J. Org. Chem.
– volume: 46
  start-page: 451
  year: 1997
  end-page: 462
  publication-title: Heterocycles
– volume: 6
  start-page: 3035
  year: 2004
  end-page: 3038
  publication-title: Org. Lett.
– start-page: 4349
  year: 2015
  end-page: 4352
  publication-title: Eur. J. Org. Chem.
– volume: 12
  start-page: 1647
  year: 2016
  end-page: 1748
  publication-title: Beilstein J. Org. Chem.
– volume: 19
  start-page: 7605
  year: 2013
  end-page: 7619
  publication-title: Chem. Eur. J.
– volume: 24
  start-page: 173
  year: 2013
  ident: e_1_2_6_29_2
  publication-title: Synlett
– ident: e_1_2_6_79_2
  doi: 10.1016/j.catcom.2016.09.028
– ident: e_1_2_6_75_2
  doi: 10.1039/c3nj01368e
– ident: e_1_2_6_45_2
  doi: 10.1039/C5GC00381D
– ident: e_1_2_6_4_2
  doi: 10.1002/ejoc.201500919
– ident: e_1_2_6_64_1
  doi: 10.1016/j.cclet.2015.01.035
– ident: e_1_2_6_12_2
  doi: 10.1021/jm9002523
– ident: e_1_2_6_49_2
  doi: 10.1016/j.tetlet.2016.12.002
– ident: e_1_2_6_16_1
  doi: 10.1016/0040-4039(91)80487-Q
– ident: e_1_2_6_17_1
  doi: 10.1139/v99-001
– ident: e_1_2_6_30_1
  doi: 10.1021/jm400004u
– ident: e_1_2_6_9_3
  doi: 10.1002/anie.200701397
– ident: e_1_2_6_66_1
  doi: 10.1016/j.catcom.2006.02.026
– ident: e_1_2_6_80_2
  doi: 10.1021/acssuschemeng.7b01102
– ident: e_1_2_6_59_2
  doi: 10.1021/acs.joc.6b02091
– ident: e_1_2_6_61_1
  doi: 10.1016/j.tet.2014.02.017
– ident: e_1_2_6_60_2
  doi: 10.1002/adsc.201600357
– ident: e_1_2_6_53_2
  doi: 10.1021/acs.joc.5b00533
– ident: e_1_2_6_81_1
  doi: 10.1016/j.mcat.2016.12.001
– ident: e_1_2_6_23_2
  doi: 10.1016/j.bmcl.2005.07.013
– ident: e_1_2_6_62_1
  doi: 10.1246/cl.140624
– ident: e_1_2_6_10_2
  doi: 10.1021/jm0610043
– ident: e_1_2_6_72_1
– ident: e_1_2_6_35_2
  doi: 10.1055/s-0030-1261225
– ident: e_1_2_6_40_2
  doi: 10.1007/s00706-009-0204-9
– ident: e_1_2_6_41_2
  doi: 10.1080/00397910802412842
– ident: e_1_2_6_69_1
– ident: e_1_2_6_67_1
  doi: 10.1016/S1872-2067(15)60829-4
– start-page: 3314
  year: 2008
  ident: e_1_2_6_70_2
  publication-title: Synthesis
– ident: e_1_2_6_74_2
  doi: 10.1002/cctc.201402415
– ident: e_1_2_6_28_2
  doi: 10.1021/ol0492142
– ident: e_1_2_6_77_2
  doi: 10.1016/j.catcom.2016.02.004
– ident: e_1_2_6_54_2
  doi: 10.1002/adsc.201500335
– ident: e_1_2_6_68_1
  doi: 10.1007/s00706-014-1275-9
– ident: e_1_2_6_6_1
– ident: e_1_2_6_58_2
  doi: 10.1002/adsc.201600565
– ident: e_1_2_6_19_1
  doi: 10.1002/hlca.19930760804
– ident: e_1_2_6_20_1
  doi: 10.3987/COM-97-S51
– ident: e_1_2_6_73_2
  doi: 10.1016/j.tet.2013.06.049
– ident: e_1_2_6_48_2
  doi: 10.1002/cplu.201600611
– ident: e_1_2_6_3_2
  doi: 10.1039/c3ob27239g
– ident: e_1_2_6_7_2
  doi: 10.1016/j.bmc.2004.08.042
– ident: e_1_2_6_51_1
– ident: e_1_2_6_47_2
  doi: 10.1021/acssuschemeng.5b01183
– ident: e_1_2_6_13_2
  doi: 10.1021/jm100678p
– ident: e_1_2_6_55_2
  doi: 10.1002/adsc.201600759
– ident: e_1_2_6_43_2
  doi: 10.1002/adsc.201100561
– ident: e_1_2_6_5_2
  doi: 10.3762/bjoc.12.162
– ident: e_1_2_6_18_1
  doi: 10.1002/hlca.19970800813
– ident: e_1_2_6_38_2
  doi: 10.1002/cmdc.201402553
– ident: e_1_2_6_27_2
  doi: 10.1021/jm301323k
– ident: e_1_2_6_14_2
  doi: 10.1021/ml300188t
– ident: e_1_2_6_39_1
– ident: e_1_2_6_76_2
  doi: 10.1016/j.apcata.2014.06.006
– ident: e_1_2_6_15_1
  doi: 10.1080/00304948.2012.697708
– ident: e_1_2_6_25_1
– volume: 21
  start-page: 3540
  year: 2009
  ident: e_1_2_6_22_2
  publication-title: Asian J. Chem.
– ident: e_1_2_6_26_2
  doi: 10.1002/chem.201300076
– ident: e_1_2_6_57_2
  doi: 10.1002/adsc.201600577
– ident: e_1_2_6_2_1
– ident: e_1_2_6_46_2
  doi: 10.1055/s-0035-1561599
– ident: e_1_2_6_50_2
  doi: 10.2174/1385272820666161020150646
– ident: e_1_2_6_42_2
  doi: 10.1039/c2ob25376c
– ident: e_1_2_6_24_2
  doi: 10.1016/j.bmcl.2010.06.045
– ident: e_1_2_6_71_2
  doi: 10.1002/adsc.201300551
– ident: e_1_2_6_31_1
  doi: 10.1002/ejoc.201500326
– ident: e_1_2_6_44_2
  doi: 10.1016/j.ccr.2015.01.001
– ident: e_1_2_6_78_2
  doi: 10.1039/C6RA19579B
– ident: e_1_2_6_21_1
– ident: e_1_2_6_8_2
  doi: 10.1351/pac200577061059
– ident: e_1_2_6_65_1
  doi: 10.1016/j.tetlet.2016.08.099
– ident: e_1_2_6_11_2
  doi: 10.1016/j.bmcl.2007.05.055
– ident: e_1_2_6_33_2
  doi: 10.2174/157017806775789903
– start-page: 2433
  year: 2005
  ident: e_1_2_6_36_2
  publication-title: Synthesis
– ident: e_1_2_6_32_1
– ident: e_1_2_6_52_2
  doi: 10.1021/cr500425u
– ident: e_1_2_6_34_2
  doi: 10.1021/ol026916n
– ident: e_1_2_6_56_2
  doi: 10.1002/adsc.201600503
– ident: e_1_2_6_9_2
  doi: 10.1002/ange.200701397
– ident: e_1_2_6_37_2
  doi: 10.1016/j.bmcl.2004.11.043
– ident: e_1_2_6_63_1
  doi: 10.1080/00397911.2016.1167910
– volume: 482
  start-page: 258
  year: 2014
  ident: WOS:000340306500031
  article-title: Magnetic CoFe2O4 nanoparticle immobilized N-propyl diethylenetriamine sulfamic acid as an efficient and recyclable catalyst for the synthesis of amides via the Ritter reaction
  publication-title: APPLIED CATALYSIS A-GENERAL
  doi: 10.1016/j.apcata.2014.06.006
– volume: 46
  start-page: 451
  year: 1997
  ident: WOS:000071491900064
  article-title: The photo-oxygenation of dihydropyrans. Formation of 1,2-dioxetanes and 1,2,4-trioxanes
  publication-title: HETEROCYCLES
– volume: 2015
  start-page: 6237
  year: 2015
  ident: WOS:000362747900013
  article-title: Energetic Organic Peroxides - Synthesis and Characterization of 1,4-Dimethyl-2,3,5,6-tetraoxabicyclo[2.2.1]heptanes
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.201500919
– start-page: 2433
  year: 2005
  ident: WOS:000231847000026
  article-title: A family of new 1,2,4-trioxanes by photooxygenation of allylic alcohols in sensitizer-doped polymers and secondary reactions
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-2005-872103
– volume: 15
  start-page: 4484
  year: 2005
  ident: WOS:000231936700016
  article-title: New orally active spiro 1,2,4-trioxanes with high antimalarial potency
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
  doi: 10.1016/j.bmcl.2005.07.013
– volume: 140
  start-page: 1481
  year: 2009
  ident: WOS:000272376400012
  article-title: A facile and efficient method for synthesis of xanthone derivatives catalyzed by HBF4/SiO2 under solvent-free conditions
  publication-title: MONATSHEFTE FUR CHEMIE
  doi: 10.1007/s00706-009-0204-9
– volume: 115
  start-page: 3170
  year: 2015
  ident: WOS:000354906800005
  article-title: Iron Catalysis in Organic Synthesis
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr500425u
– volume: 119
  start-page: 9040
  year: 2007
  ident: 000413673600025.13
  publication-title: Angew. Chem.
– volume: 4
  start-page: 1123
  year: 2016
  ident: WOS:000371755400060
  article-title: Silica-Based Magnetic Manganese Nanocatalyst - Applications in the Oxidation of Organic Halides and Alcohols
  publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING
  doi: 10.1021/acssuschemeng.5b01183
– volume: 55
  start-page: 10662
  year: 2012
  ident: WOS:000312227300030
  article-title: Bile Acid-Based 1,2,4-Trioxanes: Synthesis and Antimalarial Assessment
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1021/jm301323k
– volume: 358
  start-page: 2398
  year: 2016
  ident: WOS:000382969500008
  article-title: Iron-Catalyzed Cross-Coupling of 1-Alkynylcyclopropyl Tosylates and Related Substrates
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201600357
– volume: 76
  start-page: 2775
  year: 1993
  ident: WOS:A1993MN64900003
  article-title: SYNTHESIS, STRUCTURE, AND ANTIMALARIAL ACTIVITY OF TRICYCLIC 1,2,4-TRIOXANES RELATED TO ARTEMISININ
  publication-title: HELVETICA CHIMICA ACTA
– volume: 44
  start-page: 340
  year: 2012
  ident: WOS:000307059200002
  article-title: Recent Progress in the Synthesis of Antimalarial Agents
  publication-title: ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL
  doi: 10.1080/00304948.2012.697708
– volume: 80
  start-page: 6381
  year: 2015
  ident: WOS:000356845800040
  article-title: Reductive Alkylation of alpha-Keto Imines Catalyzed by PTSA/FeCl3: Synthesis of Indoles and 2,3 '-Biindoles
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.5b00533
– volume: 3
  start-page: 247
  year: 2006
  ident: WOS:000236167900019
  article-title: Synthetic approaches to polar antimalarial 1,2,4-trioxanes from C-5-aldehyde and ipsdienol
  publication-title: LETTERS IN ORGANIC CHEMISTRY
– volume: 7
  start-page: 787
  year: 2006
  ident: WOS:000241320000010
  article-title: Silica gel/FeCl3: An efficient and recyclable heterogenous catalyst for one step synthesis of 4(3H)-quinazolinones under solvent free conditions
  publication-title: CATALYSIS COMMUNICATIONS
  doi: 10.1016/j.catcom.2006.02.026
– volume: 32
  start-page: 7243
  year: 1991
  ident: WOS:A1991GU56900027
  article-title: REACTIONS OF AN ENDOPEROXIDE WITH CHIRAL KETONES - DIASTEREOSELECTIVE FORMATION OF 1,2,4-TRIOXANES AND 1,3-DIOXOLANES
  publication-title: TETRAHEDRON LETTERS
– volume: 52
  start-page: 3420
  year: 2009
  ident: WOS:000266296200033
  article-title: Antimalarial Peroxide Dyads from Natural Artemisinin and Hydroxyalkylated 1,2,4-Trioxanes
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1021/jm9002523
– volume: 57
  start-page: 4595
  year: 2016
  ident: WOS:000384873300021
  article-title: Silica-ferric chloride (SiO2-FeCl3) catalyzed selective synthesis of 2-substituted benzimidazole through C-sp2-C-sp3 bond cleavage of beta-ketoesteriamide
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2016.08.099
– volume: 358
  start-page: 3586
  year: 2016
  ident: WOS:000390408200010
  article-title: Iron-Catalyzed Annulation of 1,2-Diamines and Diazodicarbonyls for Diverse and Polyfunctionalized Quinoxalines, Pyrazines, and Benzoquinoxalines in Water
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201600503
– volume: 46
  start-page: 8883
  year: 2007
  ident: 000413673600025.1
  publication-title: Angew. Chem. Int. Ed.
– volume: 357
  start-page: 2862
  year: 2015
  ident: WOS:000362527100014
  article-title: Iron(III) Chloride-Catalyzed Decarboxylative-Deaminative Functionalization of Phenylglycine: A Tandem Synthesis of Quinazolinones and Benzimidazoles
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201500335
– volume: 433
  start-page: 91
  year: 2017
  ident: WOS:000400562600013
  article-title: Mesoporous silica-immobilized FeCl3 as a highly efficient and recyclable catalyst for the nitration of benzene with NO2 to nitrobenzene
  publication-title: MOLECULAR CATALYSIS
  doi: 10.1016/j.mcat.2016.12.001
– volume: 70
  start-page: 3231
  year: 2014
  ident: WOS:000335873500003
  article-title: Solvent-free Diels-Alder reactions catalyzed by FeCl3 on Aerosil((R)) silica
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2014.02.017
– volume: 26
  start-page: 735
  year: 2015
  ident: WOS:000357224900023
  article-title: A convenient synthesis of 2-aminocyclohex-1-ene-1-carboxylic esters by FeCl3/SiO2 nanoparticles as robust and efficient catalyst
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2015.01.035
– volume: 77
  start-page: 1059
  year: 2005
  ident: WOS:000230007100012
  article-title: Photooxygenation in polymer matrices: En route to highly active antimalarial peroxides
  publication-title: PURE AND APPLIED CHEMISTRY
– volume: 358
  start-page: 3683
  year: 2016
  ident: WOS:000390264700002
  article-title: Site-Selective Iron(III) Chloride-Catalyzed Arylation of 4-Aryl-4-methoxy-2,5-cyclohexadienones for the Synthesis of Polyarylated Phenols
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201600577
– volume: 88
  start-page: 39
  year: 2017
  ident: WOS:000389117500010
  article-title: Supported molybdenum on graphene oxide/Fe3O4: An efficient, magnetically separable catalyst for one-pot construction of spiro-oxindole dihydropyridines in deep eutectic solvent under microwave irradiation
  publication-title: CATALYSIS COMMUNICATIONS
  doi: 10.1016/j.catcom.2016.09.028
– volume: 5
  start-page: 6175
  year: 2017
  ident: WOS:000405139100063
  article-title: Catalyst-Free, Visible-Light Promoted One-Pot Synthesis of Spirooxindole-Pyran Derivatives in Aqueous Ethyl Lactate
  publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING
  doi: 10.1021/acssuschemeng.7b01102
– volume: 78
  start-page: 26
  year: 2016
  ident: WOS:000373418700006
  article-title: Magnetic carbon nanotube supported Cu (CoFe2O4/CNT-Cu) catalyst: A sustainable catalyst for the synthesis of 3-nitro-2-arylimidazo[1,2-a]pyridines
  publication-title: CATALYSIS COMMUNICATIONS
  doi: 10.1016/j.catcom.2016.02.004
– volume: 39
  start-page: 580
  year: 2009
  ident: WOS:000262859200002
  article-title: Fluoroboric Acid Adsorbed on Silica-Gel-Catalyzed Synthesis of 14-Aryl-14H-dibenzo[a,j]xanthene Derivatives
  publication-title: SYNTHETIC COMMUNICATIONS
  doi: 10.1080/00397910802412842
– volume: 82
  start-page: 467
  year: 2017
  ident: WOS:000398034000019
  article-title: Hexagonal Mesoporous Silica-Supported Copper Oxide (CuO/HMS) Catalyst: Synthesis of Primary Amides from Aldehydes in Aqueous Medium
  publication-title: CHEMPLUSCHEM
  doi: 10.1002/cplu.201600611
– volume: 77
  start-page: 237
  year: 1999
  ident: WOS:000079823200010
  article-title: Photochemical reaction of beta-ionone derivatives in the presence of oxygen. A convenient synthesis of substituted 1,2,4-trioxanes
  publication-title: CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE
– volume: 10
  start-page: 629
  year: 2015
  ident: WOS:000351773300007
  article-title: Selective Inhibitors of Glutathione Transferase P1 with Trioxane Structure as Anticancer Agents
  publication-title: CHEMMEDCHEM
  doi: 10.1002/cmdc.201402553
– volume: 6
  start-page: 3035
  year: 2004
  ident: WOS:000223581900005
  article-title: Application of thiol-olefin co-oxygenation methodology to a new synthesis of the 1,2,4-trioxane pharmacophore
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol0492142
– volume: 10
  start-page: 5143
  year: 2012
  ident: WOS:000305191000020
  article-title: Tandem one-pot synthesis of flavans by recyclable silica-HClO4 catalyzed Knoevenagel condensation and [4+2]-Diels-Alder cycloaddition
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/c2ob25376c
– volume: 69
  start-page: 7011
  year: 2013
  ident: WOS:000322098000010
  article-title: One-pot four-component synthesis of highly substituted pyrroles in gluconic acid aqueous solution
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2013.06.049
– volume: 20
  start-page: 4459
  year: 2010
  ident: WOS:000279866300036
  article-title: 6-(4 '-Aryloxy-phenyl)vinyl-1,2,4-trioxanes: A new series of orally active peroxides effective against multidrug-resistant Plasmodium yoelii in Swiss mice
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
  doi: 10.1016/j.bmcl.2010.06.045
– volume: 58
  start-page: 302
  year: 2017
  ident: WOS:000392896200008
  article-title: Synthesis of trans-4,5-diaminocyclopent-2-enones from furfural catalyzed by Er(III) immobilized on silica
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2016.12.002
– volume: 15
  start-page: 595
  year: 2005
  ident: WOS:000226935700020
  article-title: Novel spiroanellated 1,2,4-trioxanes with high in vitro antimalarial activities
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
  doi: 10.1016/j.bmcl.2004.11.043
– volume: 2015
  start-page: 4349
  year: 2015
  ident: WOS:000358085100011
  article-title: Model Studies on Peroxidic Glutathione Transferase (GST) Inhibitors: C5-Methylated 1,2,4-Trioxanes with C6-Acrylate Side Chains
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.201500326
– volume: 11
  start-page: 2613
  year: 2013
  ident: WOS:000316803900010
  article-title: Phosphomolybdic and phosphotungstic acids as efficient catalysts for the synthesis of bridged 1,2,4,5-tetraoxanes from beta-diketones and hydrogen peroxide
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/c3ob27239g
– volume: 53
  start-page: 7587
  year: 2010
  ident: WOS:000283703000008
  article-title: Synthesis and Antimalarial Assessment of a New Series of Orally Active Amino-Functionalized Spiro 1,2,4-Trioxanes
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1021/jm100678p
– volume: 17
  start-page: 3207
  year: 2015
  ident: WOS:000355925900002
  article-title: Silica-nanosphere-based organic-inorganic hybrid nanomaterials: synthesis, functionalization and applications in catalysis
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c5gc00381d
– volume: 24
  start-page: 173
  year: 2013
  ident: WOS:000314697700008
  article-title: Synthesis of 1,2,4-Trioxepanes and 1,2,4-Trioxanes via H2O2-Mediated Reaction of Tertiary Carbinols
  publication-title: SYNLETT
  doi: 10.1055/s-0032-1317958
– start-page: 2430
  year: 2011
  ident: WOS:000295158200031
  article-title: 5-Adamantylated 1,2,4-Trioxanes: Adamantane Position is Crucial for Antiparasitic Activity
  publication-title: SYNLETT
  doi: 10.1055/s-0030-1261225
– volume: 17
  start-page: 4097
  year: 2007
  ident: WOS:000248462300001
  article-title: Orally active antimalarials: Synthesis and bioevaluation of a new series of steroid-based 1.2.4-trioxanes against multi-drug resistant malaria in mice
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
  doi: 10.1016/j.bmcl.2007.05.055
– volume: 358
  start-page: 3471
  year: 2016
  ident: WOS:000390407300017
  article-title: Iron(III)-Catalyzed Peroxide-Mediated C-3 Functionalization of Flavones
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201600565
– start-page: 3314
  year: 2008
  ident: WOS:000260777300018
  article-title: Efficient Conversion of Epoxides into beta-Hydroperoxy Alcohols Catalyzed by Antimony Trichloride/SiO2
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-0028-1083147
– volume: 46
  start-page: 685
  year: 2016
  ident: WOS:000377815800004
  article-title: FeCl3-silica: A green approach for the synthesis of nitriles from oximes
  publication-title: SYNTHETIC COMMUNICATIONS
  doi: 10.1080/00397911.2016.1167910
– volume: 43
  start-page: 1631
  year: 2014
  ident: WOS:000343272600036
  article-title: Eco-efficient, Chemoselective, and Rapid Access to Aminals from Lactams Using Recyclable Silica-supported FeCl3 Catalyst in Green Solvent
  publication-title: CHEMISTRY LETTERS
  doi: 10.1246/cl.140624
– volume: 6
  start-page: 2854
  year: 2014
  ident: WOS:000342795000017
  article-title: Superparamagnetic CuFeO2 Nanoparticles in Deep Eutectic Solvent: an Efficient and Recyclable Catalytic System for the Synthesis of Imidazo[1,2-a]pyridines
  publication-title: CHEMCATCHEM
  doi: 10.1002/cctc.201402415
– volume: 21
  start-page: 3540
  year: 2009
  ident: WOS:000264759200030
  article-title: Synthesis of Admantane Substituted Spiro 1,2,4-Trioxanes Using Simple and Cheap Starting Material
  publication-title: ASIAN JOURNAL OF CHEMISTRY
– volume: 6
  start-page: 106160
  year: 2016
  ident: WOS:000389330700014
  article-title: Magnetically separable graphene oxide anchored sulfonic acid: a novel, highly efficient and recyclable catalyst for one-pot synthesis of 3,6-di(pyridin-3-yl)-1H-pyrazolo[3,4-b]pyridine-5-carbonitriles in deep eutectic solvent under microwave irradiation
  publication-title: RSC ADVANCES
  doi: 10.1039/c6ra19579b
– volume: 19
  start-page: 7605
  year: 2013
  ident: WOS:000319417500038
  article-title: Potent Antimalarial 1,2,4-Trioxanes through Perhydrolysis of Epoxides
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201300076
– volume: 355
  start-page: 2952
  year: 2013
  ident: WOS:000328149300029
  article-title: Magnetic Nanoparticles (CoFe2O4)-Supported Phosphomolybdate as an Efficient, Green, Recyclable Catalyst for Synthesis of beta-Hydroxy Hydroperoxides
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201300551
– volume: 146
  start-page: 165
  year: 2015
  ident: WOS:000347161300017
  article-title: FeCl3-SiO2 promoted one-pot, three-component synthesis of novel 1,5-benzodiazepine derivatives
  publication-title: MONATSHEFTE FUR CHEMIE
  doi: 10.1007/s00706-014-1275-9
– volume: 50
  start-page: 521
  year: 2007
  ident: WOS:000243889100013
  article-title: New adamantane-based spiro 1,2,4-trioxanes orally effective against rodent and simian malaria
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1021/jm0610043
– volume: 354
  start-page: 441
  year: 2012
  ident: WOS:000300448400024
  article-title: Triflic Acid-Functionalized Silica-Coated Magnetic Nanoparticles as a Magnetically Separable Catalyst for Synthesis of gem-Dihydroperoxides
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201100561
– volume: 81
  start-page: 10088
  year: 2016
  ident: WOS:000386187500063
  article-title: FeCl3-Catalyzed Cross-Dehydrogenative Coupling between Imidazoheterocycles and Oxoaldehydes
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.6b02091
– volume: 288
  start-page: 118
  year: 2015
  ident: WOS:000352252900006
  article-title: Silica-decorated magnetic nanocomposites for catalytic applications
  publication-title: COORDINATION CHEMISTRY REVIEWS
  doi: 10.1016/j.ccr.2015.01.001
– volume: 36
  start-page: 620
  year: 2015
  ident: WOS:000352678400020
  article-title: Nano-sized silica supported FeCl3 as an efficient heterogeneous catalyst for the synthesis of 1,2,4-triazine derivatives
  publication-title: CHINESE JOURNAL OF CATALYSIS
  doi: 10.1016/S1872-2067(15)60829-4
– volume: 358
  start-page: 3572
  year: 2016
  ident: WOS:000390408200009
  article-title: Iron-Promoted Tandem Cyclization of 1,3-Diynyl Chalcogen Derivatives with Diorganyl Dichalcogenides for the Synthesis of Benzo[b]furan-Fused Selenophenes
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201600759
– volume: 56
  start-page: 2547
  year: 2013
  ident: WOS:000317032200031
  article-title: Comparative Antimalarial Activities and ADME Profiles of Ozonides (1,2,4-trioxolanes) OZ277, OZ439, and Their 1,2-Dioxolane, 1,2,4-Trioxane, and 1,2,4,5-Tetraoxane Isosteres
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1021/jm400004u
– volume: 4
  start-page: 165
  year: 2013
  ident: WOS:000315182000009
  article-title: Synthesis and Antimalarial Activity of 3,3-Spiroanellated 5,6-Disubstituted 1,2,4-Trioxanes
  publication-title: ACS MEDICINAL CHEMISTRY LETTERS
  doi: 10.1021/ml300188t
– volume: 4
  start-page: 4193
  year: 2002
  ident: WOS:000179430600003
  article-title: Synthesis of antimalarial 1,2,4-trioxanes via photooxygenation of a chiral allylic alcohol
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol026916n
– volume: 12
  start-page: 1647
  year: 2016
  ident: WOS:000381258800001
  article-title: Rearrangements of organic peroxides and related processes
  publication-title: BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.3762/bjoc.12.162
– volume: 12
  start-page: 5745
  year: 2004
  ident: WOS:000225050500002
  article-title: Synthesis and antimalarial activity of 6-cycloalkylvinyl substituted 1,2,4-trioxanes
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY
  doi: 10.1016/j.bmc.2004.08.042
– volume: 21
  start-page: 368
  year: 2017
  ident: WOS:000394169000011
  article-title: Silica Supported Ionic Liquid CuCl3-IL-SiO2: A Novel and Highly Efficient Catalyst for Ullmann C-N and C-O Cross-coupling Reactions Under Mild Conditions
  publication-title: CURRENT ORGANIC CHEMISTRY
  doi: 10.2174/1385272820666161020150646
– volume: 27
  start-page: 1187
  year: 2016
  ident: WOS:000375004700012
  article-title: Site-Selective and Stereoselective C(sp(3))-H Borylation of Alkyl Side Chains of 1,3-Azoles with a Silica-Supported Monophosphine-Iridium Catalyst
  publication-title: SYNLETT
  doi: 10.1055/s-0035-1561599
– volume: 80
  start-page: 2440
  year: 1997
  ident: WOS:000071175600012
  article-title: The diastereoselective formation of 1,2,4-trioxanes and 1,3-dioxolanes by the reaction of endoperoxides with chiral cyclohexanones
  publication-title: HELVETICA CHIMICA ACTA
– volume: 38
  start-page: 2435
  year: 2014
  ident: WOS:000336821000038
  article-title: Nano-CoFe2O4 supported molybdenum as an efficient and magnetically recoverable catalyst for a one-pot, four-component synthesis of functionalized pyrroles
  publication-title: NEW JOURNAL OF CHEMISTRY
  doi: 10.1039/c3nj01368e
SSID ssj0017877
Score 2.3768413
Snippet An efficient and practical method has been developed for the facile synthesis of 1,2,4‐trioxanes by the condensation of β‐hydroperoxy alcohols and carbonyl...
An efficient and practical method has been developed for the facile synthesis of 1,2,4-trioxanes by the condensation of beta-hydroperoxy alcohols and carbonyl...
An efficient and practical method has been developed for the facile synthesis of 1,2,4-trioxanes by the condensation of [beta]-hydroperoxy alcohols and...
Source Web of Science
SourceID proquest
webofscience
crossref
wiley
SourceType Aggregation Database
Enrichment Source
Index Database
Publisher
StartPage 3618
SubjectTerms 1,2,4-trioxanes
Alcohols
Carbonyl compounds
Carbonyls
Catalysis
Catalytic activity
Chemical synthesis
Chemistry
Chemistry, Applied
Chemistry, Organic
Ferric chloride
Oxidation
Physical Sciences
Science & Technology
silica-supported iron(III) chloride
Silicon dioxide
β-hydroperoxy alcohols
Title A General and Practical Approach for the Synthesis of 1,2,4‐Trioxanes Catalyzed by Silica‐Ferric Chloride
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fadsc.201700671
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000413673600025
https://www.proquest.com/docview/1954877200
Volume 359
WOS 000413673600025
WOSCitedRecordID wos000413673600025
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpZ3NTtwwEIBHFRd6oaU_Ii0gH5B6wZA4jrM5rgIrVIkeuiBxizy2V6xasogsUpcTj8Az9knqyR8sEgLRUxJlHDnOTGbGsr8B2MEkdYR94phqx-UkQo6oQj6QmY5QEMWKNicf_1BHp_L7WXL2YBd_w4foJ9zIMur_NRm4xmr_HhqqbUUIQuLLqXoTOS3YoqjoZ8-Pirw21tVVvNvm3lOFHbUxFPvLzZe90n2oueSMluPX2gGN3oHuut6sO_m1dz3HPXPziOr4P-_2Htba6JQNG3Vahzeu_ACreVcU7iNcDFkLqma6tKyhHRlq0rLJmQ-CmQ8q2XhR-kM1rdhswqJdsSv_3t6dXE1nf7T_u7Kcpo0WN84yXLDxlKYO_f0RcSINy89pXaB1n-B0dHiSH_G2YgM3cSIjPjDWZE5FymJiVKqkDlNrE-dzX9RCoiRgnXY4UNKoic9kMiNQW0NQ-olXjvgzrJSz0m0AG1ghMEtM6nMsaUKbaW29uE0xFrF2NgDefbHCtDhzqqrxu2hAzKKgQSz6QQzgWy9_2YA8npTc7BSgaA26Kmowns9EwjCAnYdK0T-MomPi38WKvEwSQPQSsbztOhEI5gGIWiue6WAxPBjn_dWX1zT6Cm_pnJywSDZhZX517bZ8dDXH7dqC_gG8Jxui
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpZ3NbtQwEIBHVTmUC9ACIlBaHypxqdvEcZzNcRVYLf07sFuJW-SxvWJFm0XdrcT2xCPwjDwJnvy1i4SK6ClKMo4cZyYzY9nfAOxhkjrCPnFMteNyEiFHVCHvyUxHKIhiRZuTT8_U8FwefU7a1YS0F6bmQ3QTbmQZ1f-aDJwmpA9vqaHazolBSIA5RbvIH1FZ7yqr-tQRpCKvj1V9Fe-4ufdVYcttDMXhavtVv3QbbK64o9UItnJBg6eAbefrlSdfD64XeGBu_uA6PujtnsGTJkBl_VqjNmHNlVuwkbd14Z7DZZ81rGqmS8tq4JGhJg2enPk4mPm4ko2WpT_Mp3M2m7BoX-zLXz9-jq-ms-_a_2BZTjNHyxtnGS7ZaEqzh_7-gFCRhuVfaGmgdS_gfPBhnA95U7SBmziREe8ZazKnImUxMSpVUoeptYnz6S9qIVESs0477Clp1MQnM5kRqK0hLv3E60f8EtbLWeleAetZITBLTOrTLGlCm2ltvbhNMRaxdjYA3n6ywjREcyqscVHULGZR0CAW3SAG8K6T_1azPP4qud1qQNHY9Lyo2Hg-GQnDAPbuakX3MAqQCYEXK3I0SQDRv4jlTdcJQrAIQFRqcU8Hi_77Ud6dvf6fRruwMRyfnhQnH8-O38Bjuk4-WSTbsL64unZvfbC1wJ3KnH4DbCUfvQ
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpZ1LT9wwEIBHFZUKF_oA1FDa-oDEBUPiOE5yXGW7ouWhigWJW-RXxKptFrGL1OXUn9Df2F9ST16wSAgEpyjJOHKcmcyMZX8DsKmi2CL2iapYWsqLQFGlhE8TnspAMaRY4ebkwyOxd8q_nUVnt3bx13yIbsINLaP6X6OBX5hi9wYaKs0EEYTIlxO4ifwlF36Cet0_7gBSgVPHqryK89vUuSq_xTb6bHe-_bxbuok157zRfABbeaDBa5Bt3-uFJz92rqZqR1_fwTo-5-XewHITnpJerU9v4YUt38Fi1laFW4FfPdKQqoksDalxRxqbNHBy4qJg4qJKMpyV7jAZTci4IME22-b__vw9uRyNf0v3eyUZzhvNrq0hakaGI5w7dPcHCIrUJDvHhYHGrsLp4MtJtkebkg1UhxEPaKKNTq0IhFGRFrHg0o-NiaxLfpVkXHEk1kmrEsG1KFwqk2qmpNFIpS-cdoRrsFCOS_seSGIYU2mkY5dkce2bVErjxE2sQhZKazyg7RfLdcMzx7IaP_OaxMxyHMS8G0QPtjr5i5rkca_kRqsAeWPRk7wi47lUxPc92LytFN3DMDxGAF4o0M1EHgSPEcuariOCYOoBq7TigQ7mvf4w687Wn9LoM7z63h_kB1-P9j_AEl5Gh8yiDViYXl7Zjy7SmqpPlTH9BwsKHnU
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=A+General+and+Practical+Approach+for+the+Synthesis+of+1%2C2%2C4-Trioxanes+Catalyzed+by+Silica-Ferric+Chloride&rft.jtitle=Advanced+synthesis+%26+catalysis&rft.au=Zhang%2C+Mo&rft.au=Han%2C+Yi&rft.au=Niu%2C+Jia-Liang&rft.au=Zhang%2C+Zhan-Hui&rft.date=2017-10-25&rft.pub=Wiley&rft.issn=1615-4150&rft.eissn=1615-4169&rft.volume=359&rft.issue=20&rft.spage=3618&rft.epage=3625&rft_id=info:doi/10.1002%2Fadsc.201700671&rft.externalDBID=n%2Fa&rft.externalDocID=000413673600025
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1615-4150&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1615-4150&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1615-4150&client=summon