Sonochemical synthesis of 5-substituted 1 H -tetrazoles catalyzed by ZrP 2 O 7 nanoparticles and regioselective conversion into new 2,5-disubstituted tetrazoles

Abstract The ultrasound-assisted preparation of 2-(1 H -tetrazol-5-yl) acrylonitrile derivatives via a one-pot multi-component method is described successfully using ZrP 2 O 7 nanoparticles as a catalyst. Readily available tetrazoles can be transformed into the corresponding 1,5- and 2,5-disubstitut...

Full description

Saved in:
Bibliographic Details
Published inZeitschrift für Naturforschung. B, A journal of chemical sciences Vol. 70; no. 11; pp. 819 - 828
Main Authors Safaei-Ghomi, Javad, Paymard-Samani, Soleiman, Zahedi, Safura, Shahbazi-Alavi, Hossein
Format Journal Article
LanguageEnglish
Published 01.11.2015
Online AccessGet full text

Cover

Loading…
Abstract Abstract The ultrasound-assisted preparation of 2-(1 H -tetrazol-5-yl) acrylonitrile derivatives via a one-pot multi-component method is described successfully using ZrP 2 O 7 nanoparticles as a catalyst. Readily available tetrazoles can be transformed into the corresponding 1,5- and 2,5-disubstituted tetrazoles. 2,4′-Dibromoacetophenone gave the corresponding 2,5-disubstituted derivative as the only isomer. Synthesis of tetrazole derivatives with excellent yields in short times, a wide range of products under ultrasound irradiation, environmental benignity and a simple work-up procedure are some of the important features of this protocol.
AbstractList Abstract The ultrasound-assisted preparation of 2-(1 H -tetrazol-5-yl) acrylonitrile derivatives via a one-pot multi-component method is described successfully using ZrP 2 O 7 nanoparticles as a catalyst. Readily available tetrazoles can be transformed into the corresponding 1,5- and 2,5-disubstituted tetrazoles. 2,4′-Dibromoacetophenone gave the corresponding 2,5-disubstituted derivative as the only isomer. Synthesis of tetrazole derivatives with excellent yields in short times, a wide range of products under ultrasound irradiation, environmental benignity and a simple work-up procedure are some of the important features of this protocol.
Author Zahedi, Safura
Paymard-Samani, Soleiman
Shahbazi-Alavi, Hossein
Safaei-Ghomi, Javad
Author_xml – sequence: 1
  givenname: Javad
  surname: Safaei-Ghomi
  fullname: Safaei-Ghomi, Javad
  organization: Faculty of Chemistry, Department of Organic Chemistry, University of Kashan, Kashan, PO Box 87317-51167, Iran
– sequence: 2
  givenname: Soleiman
  surname: Paymard-Samani
  fullname: Paymard-Samani, Soleiman
  organization: Faculty of Chemistry, Department of Organic Chemistry, University of Kashan, Kashan, PO Box 87317-51167, Iran
– sequence: 3
  givenname: Safura
  surname: Zahedi
  fullname: Zahedi, Safura
  organization: Faculty of Chemistry, Department of Organic Chemistry, University of Kashan, Kashan, PO Box 87317-51167, Iran
– sequence: 4
  givenname: Hossein
  surname: Shahbazi-Alavi
  fullname: Shahbazi-Alavi, Hossein
  organization: Faculty of Chemistry, Department of Organic Chemistry, University of Kashan, Kashan, PO Box 87317-51167, Iran
BookMark eNpNkM1KAzEUhYNUsFWX7u8DGL2ZmUzapRT_QKigKzdDJrnRyDQpSVppn8ZH1aKgq7M4h_PBN2GjEAMxdibwQkghL3eh5xUKyREVHrCxmLaSKyHUiI1xVlcclWqP2CTnd0Qxaxocs8-nGKJ5o6U3eoC8DeWNss8QHUie130uvqwLWRBwB7xQSXoXB8pgdNHDdvfd9Ft4SY9QwQIUBB3iSqfizX6kg4VErz5mGsgUvyEwMWwoZR8D-FAiBPqA6lxy6__T_kAn7NDpIdPpbx6z55vr5_kdf1jc3s-vHriZVsj7CqfYW6Ur3damdVQ3jqyU1Uw2dqamxqG1TrfSklNOkEFjyGisHWnXN219zPjPrUkx50SuWyW_1GnbCez2drtvu93ebre3W38BOlt0dg
CitedBy_id crossref_primary_10_1515_znb_2016_0119
crossref_primary_10_1002_jhet_3961
crossref_primary_10_1002_chin_201614132
crossref_primary_10_1515_znb_2017_0178
crossref_primary_10_1515_znb_2017_0200
crossref_primary_10_3987_COM_22_14666
crossref_primary_10_1002_slct_202200706
crossref_primary_10_1007_s13738_017_1193_y
crossref_primary_10_1016_j_molstruc_2022_134507
crossref_primary_10_1002_slct_201900639
crossref_primary_10_1038_s41598_022_05993_3
crossref_primary_10_1515_znb_2017_0091
crossref_primary_10_1016_j_colcom_2023_100704
crossref_primary_10_1080_17518253_2018_1502819
crossref_primary_10_2174_1570178618666210202155047
crossref_primary_10_1016_j_ultsonch_2017_07_015
crossref_primary_10_1080_24701556_2022_2034004
crossref_primary_10_1016_j_tetlet_2020_152144
crossref_primary_10_1038_s41598_022_13011_9
crossref_primary_10_1007_s00706_018_2246_3
crossref_primary_10_1007_s11164_018_3657_9
crossref_primary_10_1007_s12039_024_02254_w
crossref_primary_10_1002_slct_202201138
Cites_doi 10.3998/ark.5550190.p008.715
10.1021/ja01632a094
10.1016/j.tet.2012.02.051
10.1016/S0040-4020(01)93173-4
10.1021/op9700340
10.1016/j.molcata.2005.11.046
10.1021/jm050033v
10.1016/j.tetlet.2004.12.073
10.1016/j.ultsonch.2011.07.011
10.1016/j.jorganchem.2005.09.046
10.1016/j.tetlet.2004.10.103
10.1007/s00706-012-0850-1
10.1021/jo01348a021
10.1016/S0959-6526(98)00026-2
10.1016/j.tetlet.2011.04.094
10.1007/s12039-013-0451-5
10.1016/j.ultsonch.2012.10.004
10.1016/j.cclet.2010.05.003
10.1016/j.tetlet.2008.02.115
10.1007/s11051-014-2590-0
10.1016/j.molcata.2014.06.001
10.1080/00397910600619630
10.1016/j.tetlet.2004.03.017
10.1021/ja0211757
10.1016/j.crci.2012.08.010
10.1016/j.ejmech.2004.03.004
10.1002/asia.200800085
10.1016/j.ultsonch.2013.04.002
10.1016/j.ultsonch.2013.11.011
10.1039/B912284B
10.1016/j.bmcl.2011.01.057
10.1007/s10593-014-1625-x
10.1016/j.ultsonch.2013.01.005
10.1021/jo062432j
10.1016/S0920-5861(97)81500-1
10.1080/00397910902917682
10.1021/jo201261w
10.1002/ejoc.201100957
10.1016/j.tetlet.2009.05.048
10.1016/j.ultsonch.2012.10.018
ContentType Journal Article
DBID AAYXX
CITATION
DOI 10.1515/znb-2015-0070
DatabaseName CrossRef
DatabaseTitle CrossRef
DatabaseTitleList CrossRef
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
Sciences (General)
EISSN 1865-7117
EndPage 828
ExternalDocumentID 10_1515_znb_2015_0070
GroupedDBID -~X
0R~
3KA
4.4
AAAEU
AAFPC
AAGVJ
AAHBH
AAILP
AAKRG
AALGR
AAONY
AAPJK
AAQCX
AASQH
AASQN
AAXCG
AAXMT
AAYXX
ABABW
ABAQN
ABDBF
ABFKT
ABJNI
ABPLS
ABRQL
ABVMU
ABWLS
ACEFL
ACGFS
ACMKP
ACNCT
ACPMA
ACXLN
ACZBO
ADEQT
ADGQD
ADGYE
ADOZN
AEDGQ
AEGVQ
AEICA
AEKEB
AEQDQ
AERZL
AFBAA
AFBQV
AFCXV
AFGNR
AFYRI
AGBEV
AGWTP
AHVWV
AHXUK
AIKXB
AKXKS
ALMA_UNASSIGNED_HOLDINGS
AMAVY
ASYPN
AZMOX
BAKPI
BBCWN
BBDJO
BCIFA
BDLBQ
CITATION
DARCH
DBYYV
E3Z
EBS
EJD
HH5
HZ~
IAO
IPNFZ
IY9
O9-
QD8
RIG
SJN
SLJYH
UK5
WTRAM
ID FETCH-LOGICAL-c820-b2080bd7a2a63c6fe34fed552954d978cf0ddfa65def7f1ec0cceca03feafb463
ISSN 0932-0776
IngestDate Thu Sep 12 19:18:03 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 11
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c820-b2080bd7a2a63c6fe34fed552954d978cf0ddfa65def7f1ec0cceca03feafb463
PageCount 10
ParticipantIDs crossref_primary_10_1515_znb_2015_0070
PublicationCentury 2000
PublicationDate 2015-11-1
PublicationDateYYYYMMDD 2015-11-01
PublicationDate_xml – month: 11
  year: 2015
  text: 2015-11-1
  day: 01
PublicationDecade 2010
PublicationTitle Zeitschrift für Naturforschung. B, A journal of chemical sciences
PublicationYear 2015
References 2021062208173296768_j_znb-2015-0070_ref_047_w2aab2b8c45b1b7b1ab2ac47Aa
2021062208173296768_j_znb-2015-0070_ref_016_w2aab2b8c45b1b7b1ab2ac16Aa
2021062208173296768_j_znb-2015-0070_ref_002_w2aab2b8c45b1b7b1ab2ab2Aa
2021062208173296768_j_znb-2015-0070_ref_029_w2aab2b8c45b1b7b1ab2ac29Aa
2021062208173296768_j_znb-2015-0070_ref_007_w2aab2b8c45b1b7b1ab2ab7Aa
2021062208173296768_j_znb-2015-0070_ref_021_w2aab2b8c45b1b7b1ab2ac21Aa
2021062208173296768_j_znb-2015-0070_ref_034_w2aab2b8c45b1b7b1ab2ac34Aa
2021062208173296768_j_znb-2015-0070_ref_026_w2aab2b8c45b1b7b1ab2ac26Aa
2021062208173296768_j_znb-2015-0070_ref_039_w2aab2b8c45b1b7b1ab2ac39Aa
2021062208173296768_j_znb-2015-0070_ref_044_w2aab2b8c45b1b7b1ab2ac44Aa
2021062208173296768_j_znb-2015-0070_ref_031_w2aab2b8c45b1b7b1ab2ac31Aa
2021062208173296768_j_znb-2015-0070_ref_013_w2aab2b8c45b1b7b1ab2ac13Aa
2021062208173296768_j_znb-2015-0070_ref_045_w2aab2b8c45b1b7b1ab2ac45Aa
2021062208173296768_j_znb-2015-0070_ref_027_w2aab2b8c45b1b7b1ab2ac27Aa
2021062208173296768_j_znb-2015-0070_ref_004_w2aab2b8c45b1b7b1ab2ab4Aa
2021062208173296768_j_znb-2015-0070_ref_005_w2aab2b8c45b1b7b1ab2ab5Aa
2021062208173296768_j_znb-2015-0070_ref_014_w2aab2b8c45b1b7b1ab2ac14Aa
2021062208173296768_j_znb-2015-0070_ref_032_w2aab2b8c45b1b7b1ab2ac32Aa
2021062208173296768_j_znb-2015-0070_ref_028_w2aab2b8c45b1b7b1ab2ac28Aa
2021062208173296768_j_znb-2015-0070_ref_046_w2aab2b8c45b1b7b1ab2ac46Aa
2021062208173296768_j_znb-2015-0070_ref_020_w2aab2b8c45b1b7b1ab2ac20Aa
2021062208173296768_j_znb-2015-0070_ref_033_w2aab2b8c45b1b7b1ab2ac33Aa
2021062208173296768_j_znb-2015-0070_ref_015_w2aab2b8c45b1b7b1ab2ac15Aa
2021062208173296768_j_znb-2015-0070_ref_038_w2aab2b8c45b1b7b1ab2ac38Aa
2021062208173296768_j_znb-2015-0070_ref_030_w2aab2b8c45b1b7b1ab2ac30Aa
2021062208173296768_j_znb-2015-0070_ref_043_w2aab2b8c45b1b7b1ab2ac43Aa
2021062208173296768_j_znb-2015-0070_ref_025_w2aab2b8c45b1b7b1ab2ac25Aa
2021062208173296768_j_znb-2015-0070_ref_012_w2aab2b8c45b1b7b1ab2ac12Aa
2021062208173296768_j_znb-2015-0070_ref_048_w2aab2b8c45b1b7b1ab2ac48Aa
2021062208173296768_j_znb-2015-0070_ref_035_w2aab2b8c45b1b7b1ab2ac35Aa
2021062208173296768_j_znb-2015-0070_ref_017_w2aab2b8c45b1b7b1ab2ac17Aa
2021062208173296768_j_znb-2015-0070_ref_008_w2aab2b8c45b1b7b1ab2ab8Aa
2021062208173296768_j_znb-2015-0070_ref_040_w2aab2b8c45b1b7b1ab2ac40Aa
2021062208173296768_j_znb-2015-0070_ref_001_w2aab2b8c45b1b7b1ab2ab1Aa
2021062208173296768_j_znb-2015-0070_ref_022_w2aab2b8c45b1b7b1ab2ac22Aa
2021062208173296768_j_znb-2015-0070_ref_018_w2aab2b8c45b1b7b1ab2ac18Aa
2021062208173296768_j_znb-2015-0070_ref_036_w2aab2b8c45b1b7b1ab2ac36Aa
2021062208173296768_j_znb-2015-0070_ref_049_w2aab2b8c45b1b7b1ab2ac49Aa
2021062208173296768_j_znb-2015-0070_ref_010_w2aab2b8c45b1b7b1ab2ac10Aa
2021062208173296768_j_znb-2015-0070_ref_041_w2aab2b8c45b1b7b1ab2ac41Aa
2021062208173296768_j_znb-2015-0070_ref_023_w2aab2b8c45b1b7b1ab2ac23Aa
2021062208173296768_j_znb-2015-0070_ref_037_w2aab2b8c45b1b7b1ab2ac37Aa
2021062208173296768_j_znb-2015-0070_ref_019_w2aab2b8c45b1b7b1ab2ac19Aa
2021062208173296768_j_znb-2015-0070_ref_003_w2aab2b8c45b1b7b1ab2ab3Aa
2021062208173296768_j_znb-2015-0070_ref_009_w2aab2b8c45b1b7b1ab2ab9Aa
2021062208173296768_j_znb-2015-0070_ref_011_w2aab2b8c45b1b7b1ab2ac11Aa
2021062208173296768_j_znb-2015-0070_ref_024_w2aab2b8c45b1b7b1ab2ac24Aa
2021062208173296768_j_znb-2015-0070_ref_006_w2aab2b8c45b1b7b1ab2ab6Aa
2021062208173296768_j_znb-2015-0070_ref_042_w2aab2b8c45b1b7b1ab2ac42Aa
References_xml – ident: 2021062208173296768_j_znb-2015-0070_ref_006_w2aab2b8c45b1b7b1ab2ab6Aa
  doi: 10.3998/ark.5550190.p008.715
– ident: 2021062208173296768_j_znb-2015-0070_ref_010_w2aab2b8c45b1b7b1ab2ac10Aa
– ident: 2021062208173296768_j_znb-2015-0070_ref_046_w2aab2b8c45b1b7b1ab2ac46Aa
  doi: 10.1021/ja01632a094
– ident: 2021062208173296768_j_znb-2015-0070_ref_041_w2aab2b8c45b1b7b1ab2ac41Aa
  doi: 10.1016/j.tet.2012.02.051
– ident: 2021062208173296768_j_znb-2015-0070_ref_008_w2aab2b8c45b1b7b1ab2ab8Aa
  doi: 10.1016/S0040-4020(01)93173-4
– ident: 2021062208173296768_j_znb-2015-0070_ref_005_w2aab2b8c45b1b7b1ab2ab5Aa
  doi: 10.1021/op9700340
– ident: 2021062208173296768_j_znb-2015-0070_ref_013_w2aab2b8c45b1b7b1ab2ac13Aa
  doi: 10.1016/j.molcata.2005.11.046
– ident: 2021062208173296768_j_znb-2015-0070_ref_030_w2aab2b8c45b1b7b1ab2ac30Aa
  doi: 10.1021/jm050033v
– ident: 2021062208173296768_j_znb-2015-0070_ref_003_w2aab2b8c45b1b7b1ab2ab3Aa
  doi: 10.1016/j.tetlet.2004.12.073
– ident: 2021062208173296768_j_znb-2015-0070_ref_044_w2aab2b8c45b1b7b1ab2ac44Aa
  doi: 10.1016/j.ultsonch.2011.07.011
– ident: 2021062208173296768_j_znb-2015-0070_ref_029_w2aab2b8c45b1b7b1ab2ac29Aa
– ident: 2021062208173296768_j_znb-2015-0070_ref_004_w2aab2b8c45b1b7b1ab2ab4Aa
  doi: 10.1016/j.jorganchem.2005.09.046
– ident: 2021062208173296768_j_znb-2015-0070_ref_027_w2aab2b8c45b1b7b1ab2ac27Aa
– ident: 2021062208173296768_j_znb-2015-0070_ref_009_w2aab2b8c45b1b7b1ab2ab9Aa
  doi: 10.1016/j.tetlet.2004.10.103
– ident: 2021062208173296768_j_znb-2015-0070_ref_026_w2aab2b8c45b1b7b1ab2ac26Aa
– ident: 2021062208173296768_j_znb-2015-0070_ref_038_w2aab2b8c45b1b7b1ab2ac38Aa
  doi: 10.1007/s00706-012-0850-1
– ident: 2021062208173296768_j_znb-2015-0070_ref_047_w2aab2b8c45b1b7b1ab2ac47Aa
  doi: 10.1021/jo01348a021
– ident: 2021062208173296768_j_znb-2015-0070_ref_034_w2aab2b8c45b1b7b1ab2ac34Aa
  doi: 10.1016/S0959-6526(98)00026-2
– ident: 2021062208173296768_j_znb-2015-0070_ref_025_w2aab2b8c45b1b7b1ab2ac25Aa
– ident: 2021062208173296768_j_znb-2015-0070_ref_048_w2aab2b8c45b1b7b1ab2ac48Aa
– ident: 2021062208173296768_j_znb-2015-0070_ref_022_w2aab2b8c45b1b7b1ab2ac22Aa
  doi: 10.1016/j.tetlet.2011.04.094
– ident: 2021062208173296768_j_znb-2015-0070_ref_039_w2aab2b8c45b1b7b1ab2ac39Aa
  doi: 10.1007/s12039-013-0451-5
– ident: 2021062208173296768_j_znb-2015-0070_ref_043_w2aab2b8c45b1b7b1ab2ac43Aa
  doi: 10.1016/j.ultsonch.2012.10.004
– ident: 2021062208173296768_j_znb-2015-0070_ref_007_w2aab2b8c45b1b7b1ab2ab7Aa
– ident: 2021062208173296768_j_znb-2015-0070_ref_019_w2aab2b8c45b1b7b1ab2ac19Aa
  doi: 10.1016/j.cclet.2010.05.003
– ident: 2021062208173296768_j_znb-2015-0070_ref_015_w2aab2b8c45b1b7b1ab2ac15Aa
  doi: 10.1016/j.tetlet.2008.02.115
– ident: 2021062208173296768_j_znb-2015-0070_ref_021_w2aab2b8c45b1b7b1ab2ac21Aa
  doi: 10.1007/s11051-014-2590-0
– ident: 2021062208173296768_j_znb-2015-0070_ref_023_w2aab2b8c45b1b7b1ab2ac23Aa
  doi: 10.1016/j.molcata.2014.06.001
– ident: 2021062208173296768_j_znb-2015-0070_ref_014_w2aab2b8c45b1b7b1ab2ac14Aa
  doi: 10.1080/00397910600619630
– ident: 2021062208173296768_j_znb-2015-0070_ref_032_w2aab2b8c45b1b7b1ab2ac32Aa
  doi: 10.1016/j.tetlet.2004.03.017
– ident: 2021062208173296768_j_znb-2015-0070_ref_036_w2aab2b8c45b1b7b1ab2ac36Aa
  doi: 10.1021/ja0211757
– ident: 2021062208173296768_j_znb-2015-0070_ref_035_w2aab2b8c45b1b7b1ab2ac35Aa
  doi: 10.1016/j.crci.2012.08.010
– ident: 2021062208173296768_j_znb-2015-0070_ref_031_w2aab2b8c45b1b7b1ab2ac31Aa
  doi: 10.1016/j.ejmech.2004.03.004
– ident: 2021062208173296768_j_znb-2015-0070_ref_002_w2aab2b8c45b1b7b1ab2ab2Aa
– ident: 2021062208173296768_j_znb-2015-0070_ref_016_w2aab2b8c45b1b7b1ab2ac16Aa
  doi: 10.1002/asia.200800085
– ident: 2021062208173296768_j_znb-2015-0070_ref_011_w2aab2b8c45b1b7b1ab2ac11Aa
– ident: 2021062208173296768_j_znb-2015-0070_ref_042_w2aab2b8c45b1b7b1ab2ac42Aa
  doi: 10.1016/j.ultsonch.2013.04.002
– ident: 2021062208173296768_j_znb-2015-0070_ref_049_w2aab2b8c45b1b7b1ab2ac49Aa
  doi: 10.1016/j.ultsonch.2013.11.011
– ident: 2021062208173296768_j_znb-2015-0070_ref_020_w2aab2b8c45b1b7b1ab2ac20Aa
  doi: 10.1039/B912284B
– ident: 2021062208173296768_j_znb-2015-0070_ref_028_w2aab2b8c45b1b7b1ab2ac28Aa
  doi: 10.1016/j.bmcl.2011.01.057
– ident: 2021062208173296768_j_znb-2015-0070_ref_040_w2aab2b8c45b1b7b1ab2ac40Aa
  doi: 10.1007/s10593-014-1625-x
– ident: 2021062208173296768_j_znb-2015-0070_ref_037_w2aab2b8c45b1b7b1ab2ac37Aa
  doi: 10.1016/j.ultsonch.2013.01.005
– ident: 2021062208173296768_j_znb-2015-0070_ref_012_w2aab2b8c45b1b7b1ab2ac12Aa
  doi: 10.1021/jo062432j
– ident: 2021062208173296768_j_znb-2015-0070_ref_033_w2aab2b8c45b1b7b1ab2ac33Aa
  doi: 10.1016/S0920-5861(97)81500-1
– ident: 2021062208173296768_j_znb-2015-0070_ref_018_w2aab2b8c45b1b7b1ab2ac18Aa
  doi: 10.1080/00397910902917682
– ident: 2021062208173296768_j_znb-2015-0070_ref_024_w2aab2b8c45b1b7b1ab2ac24Aa
  doi: 10.1021/jo201261w
– ident: 2021062208173296768_j_znb-2015-0070_ref_045_w2aab2b8c45b1b7b1ab2ac45Aa
  doi: 10.1002/ejoc.201100957
– ident: 2021062208173296768_j_znb-2015-0070_ref_017_w2aab2b8c45b1b7b1ab2ac17Aa
  doi: 10.1016/j.tetlet.2009.05.048
– ident: 2021062208173296768_j_znb-2015-0070_ref_001_w2aab2b8c45b1b7b1ab2ab1Aa
  doi: 10.1016/j.ultsonch.2012.10.018
SSID ssj0019440
Score 2.067307
Snippet Abstract The ultrasound-assisted preparation of 2-(1 H -tetrazol-5-yl) acrylonitrile derivatives via a one-pot multi-component method is described successfully...
SourceID crossref
SourceType Aggregation Database
StartPage 819
Title Sonochemical synthesis of 5-substituted 1 H -tetrazoles catalyzed by ZrP 2 O 7 nanoparticles and regioselective conversion into new 2,5-disubstituted tetrazoles
Volume 70
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLa27gFeEBtM3OUHhEDGo7k4aR7bwqiQYEgp0tSXyontNRJNUJpOan8NP5Xj2E3SsYfBS1SldZz0fDkX-zvnIPQ6gqhHhBGnUr9ufuI5NGE8oipiEhwKxtO6Z-TXb8Hkh__lkl0eHJ52WEvrKjlLt7fmlfyPVOEcyFVnyf6DZJuLwgn4DPKFI0gYjneScVzkuuGVyfhfbXJw5mx9EUZXoBEMDUAQh0wIrWRV8q2u30TqNZvN1jifs_I7cckFCUnOcwihLVPOEM_lVVas6lY5mmFUU9Tr9TVdZqLQ7ciJC0JiVGTd-dqpur7vTGYVxNJlpiqi9Ab9aFxqsvRaE-zhC1A7Z2RklFWnoEX7gEYNNUFAzBWXGf28KJaZIfxec9FuiW2Wmg8c86XpWkViuJ9s2b4MM74Aw21WxdW6bMxTvOCLhG8zOvzJr01Pb3AkpK1QbhdIHGYzBTsrnZ4m2Ia24rbR84OA0dAxaaM7Q2A6mOwA73TU-sCqdeshmHT2v4wPq-t0bPOE1rehKym1VnbHLLhhfBtKpA7G4AJzGD7Xw-d6-CE6csOIhT10NBx9HJ03-2ORX6f6No9mq8fCBT7szd_xtjpu0_QhemDjHTw0qDpGBzI_QffGuzaDJ-jYWpcVfmtLoL97hH53kY0bZONC4T1kYwdPcAfZuEE2TjYYkI1dfIFDvIdsDMjG-8jGLbKxRjYGZGP3_Q1c43aix2h6_mk6nlDbS4Sm4OPSxIXIKBEhd3ngpYGSnq-kYPUut4jCQar6QigeMCFVqByZ9tNUprzvKclV4gfeKerlRS6fIJymuiODGPhMKd8XQcKYJ0Qgua-cYBCpp-jN7i-f_zIVY-a3CvfZXX_4HN1vcf0C9apyLV-CK1wlrywu_gCDXryD
link.rule.ids 315,786,790,27957,27958
linkProvider EBSCOhost
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=Sonochemical+synthesis+of+5-substituted+1+H+-tetrazoles+catalyzed+by+ZrP+2+O+7+nanoparticles+and+regioselective+conversion+into+new+2%2C5-disubstituted+tetrazoles&rft.jtitle=Zeitschrift+f%C3%BCr+Naturforschung.+B%2C+A+journal+of+chemical+sciences&rft.au=Safaei-Ghomi%2C+Javad&rft.au=Paymard-Samani%2C+Soleiman&rft.au=Zahedi%2C+Safura&rft.au=Shahbazi-Alavi%2C+Hossein&rft.date=2015-11-01&rft.issn=0932-0776&rft.eissn=1865-7117&rft.volume=70&rft.issue=11&rft.spage=819&rft.epage=828&rft_id=info:doi/10.1515%2Fznb-2015-0070&rft.externalDBID=n%2Fa&rft.externalDocID=10_1515_znb_2015_0070
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0932-0776&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0932-0776&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0932-0776&client=summon