Static to inducibly dynamic stereocontrol: The convergent use of racemic β-substituted ketones

Author:

DeHovitz Jacob S.1ORCID,Loh Yong Yao1ORCID,Kautzky Jacob A.1,Nagao Kazunori1ORCID,Meichan Andrew J.1,Yamauchi Motoshi1ORCID,MacMillan David W. C.1ORCID,Hyster Todd K.1ORCID

Affiliation:

1. Merck Center for Catalysis, Princeton University, Princeton, NJ 08544, USA.

Abstract

Expanding the kinetic resolution purview Dynamic kinetic resolution (DKR) is a powerful method to transform a pair of mirror-image reactants into just one of the two possible mirror-image products. The key is to find a means of rapidly interconverting the reactants while one of them is being more efficiently funneled to product. DeHovitz et al. report cooperative application of organocatalysis, photoredox catalysis, and enzymatic catalysis to achieve DKR of β-substituted ketones into chiral alcohols. This β position has typically been considered too configurationally stable for a DKR approach. Science , this issue p. 1113

Funder

National Science Foundation

U.S. Department of Energy

Alfred P. Sloan Foundation

Bristol-Myers Squibb Foundation

Searle Scholars Program

A*STAR

ACS-PRF

JSPS

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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