Deciphering the roles of multiple additives in organocatalyzed Michael additions
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Supporting information
Author(s)
Type
Journal Article
Abstract
The synergistic effects of multiple additives (water and acetic acid) on the asymmetric Michael addition of acetone to nitrostyrene catalyzed by primary amine-thioureas (PAT) were precisely determined. Acetic acid facilitates hydrolysis of the imine intermediates, thus leading to catalytic behavior, and minimizes the formation of the double addition side product. In contrast, water slows down the reaction but minimizes catalyst deactivation, eventually leading to higher final yields.
Date Issued
2016-04-25
Date Acceptance
2016-04-25
Citation
Chemical Communications, 2016, 52 (41), pp.6821-6824
ISSN
1364-548X
Publisher
Royal Society of Chemistry
Start Page
6821
End Page
6824
Journal / Book Title
Chemical Communications
Volume
52
Issue
41
Copyright Statement
© Royal Society of Chemistry 2016
Sponsor
Research Executive Agency
Imperial College London
Subjects
Science & Technology
Physical Sciences
Chemistry, Multidisciplinary
Chemistry
DIRECT CONJUGATE ADDITION
ASYMMETRIC ALDOL REACTION
AMINE-THIOUREA CATALYST
BIFUNCTIONAL ORGANOCATALYSTS
MECHANISTIC RATIONALIZATION
1,3-DICARBONYL COMPOUNDS
ALPHA-AMINATION
CONTINUOUS-FLOW
WATER
NITROALKENES
Organic Chemistry
03 Chemical Sciences
Publication Status
Published