ChemInform Abstract: Enantioselective Synthesis of 2‐Amino‐3‐nitrile‐chromenes Catalyzed by Cinchona Alkaloids: A Remarkable Additive Effect. Issue 22 (12th May 2016)

Record Type:: Journal Article
Title:: ChemInform Abstract: Enantioselective Synthesis of 2‐Amino‐3‐nitrile‐chromenes Catalyzed by Cinchona Alkaloids: A Remarkable Additive Effect. Issue 22 (12th May 2016)
Main Title:: ChemInform Abstract: Enantioselective Synthesis of 2‐Amino‐3‐nitrile‐chromenes Catalyzed by Cinchona Alkaloids: A Remarkable Additive Effect.
Authors:: Zheng, Yuan‐Qin
Luan, Chun‐Feng
Wang, Zhi‐Jing
Yao, Yong‐Qi
Shi, Zhi‐Chuan
Li, Xue‐Feng
Zhao, Zhi‐Gang
Chen, Feng
Abstract:: Abstract: An efficient methodology to form 2‐amino‐3‐nitrile chromenes, compounds with significant antitumor activity, from readily available functionalized chalcones and malononitrile is developed.
Is Part Of:: ChemInform. Volume 47:Issue 22(2016)
Journal:: ChemInform
Issue:: Volume 47:Issue 22(2016)
Issue Display:: Volume 47, Issue 22 (2016)
Year:: 2016
Volume:: 47
Issue:: 22
Issue Sort Value:: 2016-0047-0022-0000
Page Start:: no
Page End:: no
Publication Date:: 2016-05-12
Subjects:: diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) -- benzopyran derivatives -- ring closure reactions, annulation reactions
Chemistry -- Abstracts -- Periodicals
540.5
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1522-2667 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/chin.201622024 ↗
Languages:: English
ISSNs:: 0931-7597
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3158.195000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 2571.xml