The use of hydrazones for efficient mannich type coupling with aldehydes and secondary amines

The Mannich reaction of hydrazones originally limited to the coupling of hydrazones with formaldehyde has been extended to a large variety of aldehydes through appropriate selection of experimental conditions; in conjunction with the Japp-Klingmann reaction, this process provides an efficient synthe...

Full description

Saved in:
Bibliographic Details
Published inChemical communications (Cambridge, England) no. 17; pp. 1585 - 1586
Main Authors Atlan, Bienayme, H, El Kaim, L, Majee, A
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 01.01.2000
Subjects
Online AccessGet full text

Cover

Loading…
Abstract The Mannich reaction of hydrazones originally limited to the coupling of hydrazones with formaldehyde has been extended to a large variety of aldehydes through appropriate selection of experimental conditions; in conjunction with the Japp-Klingmann reaction, this process provides an efficient synthetic tool for the formation of carbon-carbon bonds.
AbstractList The Mannich reaction of hydrazones originally limited to the coupling of hydrazones with formaldehyde has been extended to a large variety of aldehydes through appropriate selection of experimental conditions; in conjunction with the Japp-Klingmann reaction, this process provides an efficient synthetic tool for the formation of carbon-carbon bonds.
Author Majee, A
Atlan
El Kaim, L
Bienayme, H
Author_xml – sequence: 1
  surname: Atlan
  fullname: Atlan
– sequence: 2
  givenname: H
  surname: Bienayme
  fullname: Bienayme, H
– sequence: 3
  givenname: L
  surname: El Kaim
  fullname: El Kaim, L
– sequence: 4
  givenname: A
  surname: Majee
  fullname: Majee, A
BookMark eNqNkNtKAzEQhoNUsK2Cj5BLQVaTzWGTS1k8QcGbCt7Iks3BjXSTstlS6tObpeq1w8DMwDc_M_8CzEIMFoBLjG4wIvK2RaisGOpPwBwTTgtGxdts6pksKkLZGVik9IlyYCbm4H3dWbhLFkYHu4MZ1FeWS9DFAVrnvPY2jLBXIXjdwfGwtVDH3Xbjwwfc-7GDamNs3ssrKhiYrI7BqOEAVe-zzjk4dWqT7MVPXYLXh_t1_VSsXh6f67tVocuSjYUQklTEaUSwQ0oyxFEppeOiJYZrk0fFDLc5McUt4oYbWuGKcqqxtFKQJbg66uohpjRY12wH3-c7GoyayZbm15aMXh_RvW2jS9OD2v7hky_5GkzFZBDJtPg_XftRjT6GOu7CSL4BLal34Q
CitedBy_id crossref_primary_10_1002_1099_0682_20022_2002_2_481__AID_EJIC481_3_0_CO_2_0
crossref_primary_10_1002_chin_200048045
crossref_primary_10_1021_om060953r
crossref_primary_10_1039_C6CC08171A
crossref_primary_10_1039_C5RA12715G
crossref_primary_10_1002_ejoc_201100261
crossref_primary_10_1039_B306242B
crossref_primary_10_1081_SCC_120027244
crossref_primary_10_1016_S0040_4039_02_01977_9
crossref_primary_10_1016_S0020_1693_02_00708_9
crossref_primary_10_1016_j_tetlet_2007_03_164
crossref_primary_10_1002_anie_201702295
crossref_primary_10_1016_j_tetlet_2010_09_098
crossref_primary_10_1039_B610229H
crossref_primary_10_1039_C7OB02840G
crossref_primary_10_1002_ejoc_201300787
crossref_primary_10_1002_ejoc_200700746
crossref_primary_10_1002_jhet_5570440118
crossref_primary_10_1002_ange_201702295
crossref_primary_10_3184_030823405774909441
ContentType Journal Article
DBID 1KM
1KN
BLEPL
DTL
FKBAJ
AAYXX
CITATION
DOI 10.1039/b002750m
DatabaseName Index Chemicus
Current Chemical Reactions
Web of Science Core Collection
Science Citation Index Expanded
Web of Science - Science Citation Index Expanded - 2000
CrossRef
DatabaseTitle Web of Science
CrossRef
DatabaseTitleList Web of Science
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 1364-548X
EndPage 1586
ExternalDocumentID 10_1039_b002750m
000088914800013
GroupedDBID ---
-DZ
-JG
-~X
0-7
0R~
186
1KM
1KN
1TJ
29B
2WC
3EH
4.4
53G
5GY
6J9
6TJ
705
70~
7~J
9M8
AAEMU
AAHBH
AAMEH
AANOJ
AAXHV
AAXPP
ABEMK
ABJNI
ABPDG
ABXOH
ACBEA
ACGFO
ACGFS
ACHDF
ACIWK
ACLDK
ACMRT
ACNCT
ADSRN
AEFDR
AENEX
AESAV
AFFNX
AGKEF
AGRSR
AGSTE
AHGXI
AI.
ALMA_UNASSIGNED_HOLDINGS
ANLMG
ANUXI
ASPBG
AVWKF
AZFZN
BBWZM
BLAPV
BLEPL
BSQNT
C6K
CAG
COF
CS3
DTL
DU5
EBS
EE0
EEHRC
EF-
EJD
F20
F5P
FEDTE
GNO
GROUPED_WOS_SCIENCE_CITATION_INDEX_EXPANDED
H13
HVGLF
HZ~
H~N
IDY
IDZ
IH2
J3G
J3H
J3I
KC5
L-8
M4U
MVM
N9A
NDZJH
O9-
P2P
R56
R7B
R7D
RAOCF
RCNCU
RNS
ROL
RPMJG
RRA
RRC
SJN
SKA
SKF
SKH
SLH
TN5
TWZ
UHB
UPT
VH1
VH6
VQA
WH7
XJT
ZCG
0UZ
71~
AAIWI
AAJAE
AAWGC
AAYOK
AAYXX
ABASK
ABDVN
ABRYZ
ADMRA
AENGV
AETIL
AFLYV
AFOGI
AFRDS
AFVBQ
AGEGJ
AHGCF
ANBJS
APEMP
ASKNT
AUDPV
CITATION
ECGLT
FA8
GGIMP
OHT
R7C
RCLXC
RIG
RRXOS
RSCEA
WHG
X7L
ZKB
ID FETCH-LOGICAL-c225t-889373fc031f0a95060299f68b3d6cd060a5d6ed6e141b06d6d4717464c19e983
IEDL.DBID RRA
ISICitedReferencesCount 30
ISICitedReferencesURI https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000088914800013
ISSN 1359-7345
IngestDate Fri Aug 23 02:57:07 EDT 2024
Tue Sep 17 23:32:39 EDT 2024
Fri Oct 18 19:52:22 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 17
Language English
LinkModel DirectLink
LogoURL https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg
MergedId FETCHMERGED-LOGICAL-c225t-889373fc031f0a95060299f68b3d6cd060a5d6ed6e141b06d6d4717464c19e983
PageCount 2
ParticipantIDs webofscience_primary_000088914800013
webofscience_primary_000088914800013CitationCount
crossref_primary_10_1039_b002750m
PublicationCentury 2000
PublicationDate 2000-01-01
PublicationDateYYYYMMDD 2000-01-01
PublicationDate_xml – month: 01
  year: 2000
  text: 2000-01-01
  day: 01
PublicationDecade 2000
PublicationPlace CAMBRIDGE
PublicationPlace_xml – name: CAMBRIDGE
PublicationTitle Chemical communications (Cambridge, England)
PublicationTitleAbbrev CHEM COMMUN
PublicationYear 2000
Publisher Royal Soc Chemistry
Publisher_xml – name: Royal Soc Chemistry
References SEEBACH, D (WOS:A1984TK76500025) 1984; 67
KLEINMAN EF (WOS:000088914800013.3) 1991; 2
Attanasi, OA (WOS:A1997YG33000002) 1997
RIED, W (WOS:A1957WU15600020) 1957; 605
Yamada, K (WOS:000084141900018) 1999; 38
References_xml – volume: 2
  start-page: 893
  year: 1991
  ident: WOS:000088914800013.3
  publication-title: COMPREHENSIVE ORGANI
  contributor:
    fullname: KLEINMAN EF
– volume: 67
  start-page: 1593
  year: 1984
  ident: WOS:A1984TK76500025
  article-title: DIASTEREOSELECTIVE SYNTHESIS OF NOVEL MANNICH-BASES) THROUGH TITANIUM REAGENTS
  publication-title: HELVETICA CHIMICA ACTA
  contributor:
    fullname: SEEBACH, D
– volume: 605
  start-page: 167
  year: 1957
  ident: WOS:A1957WU15600020
  article-title: BEITRAGE ZUR MANNICH-REAKTION
  publication-title: ANNALEN DER CHEMIE-JUSTUS LIEBIG
  contributor:
    fullname: RIED, W
– volume: 38
  start-page: 3504
  year: 1999
  ident: WOS:000084141900018
  article-title: The first catalytic asymmetric nitro-Mannich-type reaction promoted by a new heterobimetallic complex
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  contributor:
    fullname: Yamada, K
– start-page: 1128
  year: 1997
  ident: WOS:A1997YG33000002
  article-title: Working twenty years on conjugated azo-alkenes (and environs) to find new entries in organic synthesis
  publication-title: SYNLETT
  contributor:
    fullname: Attanasi, OA
SSID ssj0000158
Score 1.7983987
Snippet The Mannich reaction of hydrazones originally limited to the coupling of hydrazones with formaldehyde has been extended to a large variety of aldehydes through...
Source Web of Science
SourceID crossref
webofscience
SourceType Aggregation Database
Enrichment Source
Index Database
StartPage 1585
SubjectTerms Chemistry
Chemistry, Multidisciplinary
Physical Sciences
Science & Technology
Title The use of hydrazones for efficient mannich type coupling with aldehydes and secondary amines
URI http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000088914800013
WOS 000088914800013
WOSCitedRecordID wos000088914800013
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1LawIxEB7ES3vpu9S-SIvXFddk4-YoS0UK7aFU8FIkm0eFVi26HvTXd2bXLZY-EPaykGRDMrPfl8d8A1AXLSNC51zQNnEUkIUEsVNNCvCJOLqT95pihx8eZa8v7gfRoAK3f5zgc0VZDkmDfEy_WUQjWpA_dTYUovIUnCGPVNDmIir1ZTcqfkOcX9AlR5LuPiRlPE5xgeStscjShln9lGf8p5MHsLcmkqxTzPwhVNzkCHaSMn_bMbygBbDF3LGpZ6OlnekVyfIzJKnM5boRCDdsTCmLzIjRTiwz0wXF574y2pxl-t06rIdV9MSyOS2crZ4tmR7TTfkT6HfvnpNesE6mEBh02SyIiZhwb9CJfVMr0hVEJPIyTrmVxuKrjqx0-IQiTJvSSou41RZSmFA5FfNTqE6wn2fAQmlbnrTsvNQi9jxFVhAaoaTWqce2anBTDvjwo9DMGOZn3VwNy4GqQX1zJr7K5Rw2VrhIy9lpDcJtiiVrPXOK48_Ot_j8BewWMfW0l3IJ1Wy2cFfILrL0OrevTw2vyfk
link.rule.ids 315,786,790,2812,27955,27956
linkProvider Royal Society of Chemistry
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=The+use+of+hydrazones+for+efficient+mannich+type+coupling+with+aldehydes+and+secondary+amines&rft.jtitle=Chemical+communications+%28Cambridge%2C+England%29&rft.au=Atlan%2C+Val%C3%A9rie&rft.au=Bienaym%C3%A9%2C+Hugues&rft.au=El+Kaim%2C+Laurent&rft.au=Majee%2C+Adinath&rft.date=2000-01-01&rft.issn=1359-7345&rft.eissn=1364-548X&rft.issue=17&rft.spage=1585&rft.epage=1586&rft_id=info:doi/10.1039%2Fb002750m&rft.externalDBID=n%2Fa&rft.externalDocID=10_1039_b002750m
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1359-7345&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1359-7345&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1359-7345&client=summon