ChemInform Abstract: Mukaiyama—Michael Reactions with trans‐2, 5‐Diarylpyrrolidine Catalysts: Enantioselectivity Arises from Attractive Noncovalent Interactions, Not from Steric Hindrance. Issue 42 (14th October 2014)

Record Type:: Journal Article
Title:: ChemInform Abstract: Mukaiyama—Michael Reactions with trans‐2, 5‐Diarylpyrrolidine Catalysts: Enantioselectivity Arises from Attractive Noncovalent Interactions, Not from Steric Hindrance. Issue 42 (14th October 2014)
Main Title:: ChemInform Abstract: Mukaiyama—Michael Reactions with trans‐2, 5‐Diarylpyrrolidine Catalysts: Enantioselectivity Arises from Attractive Noncovalent Interactions, Not from Steric Hindrance.
Authors:: Kemppainen, Eeva K.
Sahoo, Gokarneswar
Piisola, Antti
Hamza, Andrea
Kotai, Bianka
Papai, Imre
Pihko, Petri M.
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The 2, 5‐diphenylpyrrolidine‐catalyzed enantioselective Mukaiyama—Michael reaction between substituted furans and enals is studied.</p> </abstract>
Is Part Of:: ChemInform. Volume 45:Issue 42(2014)
Journal:: ChemInform
Issue:: Volume 45:Issue 42(2014)
Issue Display:: Volume 45, Issue 42 (2014)
Year:: 2014
Volume:: 45
Issue:: 42
Issue Sort Value:: 2014-0045-0042-0000
Page Start:: no
Page End:: no
Publication Date:: 2014-10-14
Subjects:: 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.201442019 ↗
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:: 3398.xml