2015年7月
Organocatalytic Activation of the Leaving Group in the Intramolecular Asymmetric S(N)2 ' Reaction
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
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- 巻
- 54
- 号
- 28
- 開始ページ
- 8263
- 終了ページ
- 8266
- 記述言語
- 英語
- 掲載種別
- 研究論文（学術雑誌）
- DOI
- 10.1002/anie.201502831
- 出版者・発行元
- WILEY-V C H VERLAG GMBH
A BrOnsted-acid-catalyzed intramolecular enantioselective S(N)2 reaction was developed utilizing trichloroacetimidate as a leaving group. The findings indicated that dual activation of the substrates is operative. This metal-free allylic alkylation allows highly enantioselective access to 2-vinylpyrrolidines bearing various substituents.
- リンク情報
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- DOI
- https://doi.org/10.1002/anie.201502831
- J-GLOBAL
- https://jglobal.jst.go.jp/detail?JGLOBAL_ID=201502219351490553
- PubMed
- https://www.ncbi.nlm.nih.gov/pubmed/26016987
- Web of Science
- https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000357209000044&DestApp=WOS_CPL
- URL
- http://www.scopus.com/inward/record.url?eid=2-s2.0-84933525336&partnerID=MN8TOARS
- URL
- http://orcid.org/0000-0002-1798-7919
- ID情報
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- DOI : 10.1002/anie.201502831
- ISSN : 1433-7851
- eISSN : 1521-3773
- J-Global ID : 201502219351490553
- ORCIDのPut Code : 45409572
- PubMed ID : 26016987
- SCOPUS ID : 84933525336
- Web of Science ID : WOS:000357209000044