ChemInform Abstract: (1, 2‐Diaminoethane‐1, 2‐diyl)bis(N‐methylpyridinium) Salts as a Prospective Platform for Designing Recyclable Prolinamide‐Based Organocatalysts. Issue 9 (February 2016)

Record Type:: Journal Article
Title:: ChemInform Abstract: (1, 2‐Diaminoethane‐1, 2‐diyl)bis(N‐methylpyridinium) Salts as a Prospective Platform for Designing Recyclable Prolinamide‐Based Organocatalysts. Issue 9 (February 2016)
Main Title:: ChemInform Abstract: (1, 2‐Diaminoethane‐1, 2‐diyl)bis(N‐methylpyridinium) Salts as a Prospective Platform for Designing Recyclable Prolinamide‐Based Organocatalysts.
Authors:: Lisnyak, Vladislav G.
Kucherenko, Alexander S.
Valeev, Edward F.
Zlotin, Sergei G.
Abstract:: Abstract: A new, efficient, and recyclable organocatalyst for asymmetric cross‐aldol reactions under neat conditions in ketone—ketone, ketone—aldehyde, and aldehyde—aldehyde systems is developed.
Is Part Of:: ChemInform. Volume 47:Issue 9(2016)
Journal:: ChemInform
Issue:: Volume 47:Issue 9(2016)
Issue Display:: Volume 47, Issue 9 (2016)
Year:: 2016
Volume:: 47
Issue:: 9
Issue Sort Value:: 2016-0047-0009-0000
Page Start:: no
Page End:: no
Publication Date:: 2016-02
Subjects:: diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) -- C‐C bond formation -- addition reactions -- organocatalysis -- ketones (acyclic compounds) -- hydroxycarboxylic acids (ether carboxylic acids) (acyclic compounds) and esters
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.201609021 ↗
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:: 536.xml