Published May 2013
| Accepted Version
Journal Article
Open
The Construction of All-Carbon Quaternary Stereocenters by Use of Pd-Catalyzed Asymmetric Allylic Alkylation Reactions in Total Synthesis
- Creators
- Hong, Allen Y.
-
Stoltz, Brian M.
Chicago
Abstract
All-carbon quaternary stereocenters have posed significant challenges in the synthesis of complex natural products. These important structural motifs have inspired the development of broadly applicable palladium-catalyzed asymmetric allylic alkylation reactions of unstabilized non-biased enolates for the synthesis of enantioenriched α-quaternary products. This microreview outlines key considerations in the application of palladium-catalyzed asymmetric allylic alkylation reactions and presents recent total syntheses of complex natural products that have employed these powerful transformations for the direct, catalytic, enantioselective construction of all-carbon quaternary stereocenters.
Additional Information
© 2013 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. Received: December 30, 2012; Published Online: March 27, 2013. The authors thank National Institutes of Health – National Institute of General Medical Sciences (grant number R01GM080269- 01), Roche, Abbott Laboratories, Amgen, Boehringer Ingelheim, the Gordon and Betty Moore Foundation, and Caltech for awards and financial support. Nick O'Connor, Kelly Kim, and Christopher Haley are acknowledged for editorial assistance.Attached Files
Accepted Version - nihms582798.pdf
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nihms582798.pdf
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Additional details
- PMCID
- PMC4059687
- Eprint ID
- 39005
- DOI
- 10.1002/ejoc.201201761
- Resolver ID
- CaltechAUTHORS:20130620-142930731
- NIH
- R01GM080269-01
- Roche
- Abbott Laboratories
- Amgen
- Boehringer Ingelheim
- Gordon and Betty Moore Foundation
- Caltech
- Created
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2013-06-21Created from EPrint's datestamp field
- Updated
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2021-11-09Created from EPrint's last_modified field