Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
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

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
Files (16.5 MB)
Name Size Download all
md5:e3459069389a7ccdf0e0d7ed8246374c
14.5 MB Preview Download
md5:e7d83d78e61f60450f60b7d6d47fd41b
1.3 MB Preview Download
md5:cd81531ef3eee851731d75d31114eb9a
724.0 kB Preview Download

Additional details

Created:
August 19, 2023
Modified:
October 18, 2023