ChemInform Abstract: Direct Construction of Chiral Quaternary Dihydropyranones Through Highly Enantioselective Organocatalytic hetero‐Diels—Alder Reactions of Olefinic Azlactones. Issue 36 (August 2016)

Record Type:: Journal Article
Title:: ChemInform Abstract: Direct Construction of Chiral Quaternary Dihydropyranones Through Highly Enantioselective Organocatalytic hetero‐Diels—Alder Reactions of Olefinic Azlactones. Issue 36 (August 2016)
Main Title:: ChemInform Abstract: Direct Construction of Chiral Quaternary Dihydropyranones Through Highly Enantioselective Organocatalytic hetero‐Diels—Alder Reactions of Olefinic Azlactones.
Authors:: Gao, Tai‐Ping
Liu, Dan
Lin, Jun‐Bing
Hu, Xiu‐Qin
Wang, Zhu‐Yin
Xu, Peng‐Fei
Abstract:: Abstract: For the first time, an enantioselective hetero‐Diels—Alder reaction of an in situ generated diene with β, γ‐unsaturated α‐keto esters or α‐keto esters is reported.
Is Part Of:: ChemInform. Volume 47:Issue 36(2016)
Journal:: ChemInform
Issue:: Volume 47:Issue 36(2016)
Issue Display:: Volume 47, Issue 36 (2016)
Year:: 2016
Volume:: 47
Issue:: 36
Issue Sort Value:: 2016-0047-0036-0000
Page Start:: no
Page End:: no
Publication Date:: 2016-08
Subjects:: pyran derivatives -- amide formation -- carboxylic amides (benzene compounds) -- organocatalysis -- diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) -- cycloaddition 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.201636145 ↗
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:: 1740.xml