Published August 15, 2018
| Supplemental Material + Accepted Version
Journal Article
Open
Catalytic Enantioselective Synthesis of Acyclic Quaternary Centers: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Acyclic Enol Carbonates
- Creators
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Alexy, Eric J.
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Zhang, Haiming
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Stoltz, Brian M.
Chicago
Abstract
The first enantioselective palladium-catalyzed decarboxylative allylic alkylation of fully substituted acyclic enol carbonates providing linear α-quaternary ketones is reported. Investigation into the reaction revealed that the use of an electron-deficient phosphinooxazoline ligand renders the enolate geometry of the starting material inconsequential, with the same enantiomer of product obtained in the same level of selectivity regardless of the starting ratio of enolates. As a result, a general method toward acyclic all-carbon quaternary stereocenters has been developed.
Additional Information
© 2018 American Chemical Society. Received: May 27, 2018; Published: July 26, 2018. We thank NIH-NIGMS (R01GM080269), the Gordon and Betty Moore Foundation, and Caltech for financial support. E.J.A. thanks the National Science Foundation for a predoctoral fellowship. We thank Dr. David VanderVelde (Caltech) for NMR expertise. Dr. Scott Virgil (Caltech) is thanked for instrumentation and SFC assistance. The authors declare no competing financial interest.Attached Files
Accepted Version - nihms985449.pdf
Supplemental Material - ja8b05560_si_001.pdf
Supplemental Material - ja8b05560_si_002.pdf
Files
ja8b05560_si_002.pdf
Additional details
- PMCID
- PMC6103296
- Eprint ID
- 88319
- Resolver ID
- CaltechAUTHORS:20180727-091530074
- NIH
- R01GM080269
- Gordon and Betty Moore Foundation
- Caltech
- NSF Predoctoral Fellowship
- Created
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2018-07-30Created from EPrint's datestamp field
- Updated
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2022-03-04Created from EPrint's last_modified field