Response to Comment on “Asymmetric syntheses of sceptrin and massadine and evidence for biosynthetic enantiodivergence”

Author:

Ma Zhiqiang1,Wang Xiaolei1,Wang Xiao1,Rodriguez Rodrigo A.2,Moore Curtis E.3,Gao Shuanhu1,Tan Xianghui1,Ma Yuyong1,Rheingold Arnold L.3,Baran Phil S.2,Chen Chuo1

Affiliation:

1. Department of Biochemistry, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

2. Department of Chemistry, The Scripps Research Institute, La Jolla, CA 92037, USA.

3. Department of Chemistry and Biochemistry, University of California San Diego, La Jolla, CA 92093, USA.

Abstract

Sherman et al . commented on the precedence of enantiodivergence, listing a number of congeneric natural products with opposite chirality. However, these “congeners” are not derived from enantiodivergent biosyntheses. Instead, they are antipodes arising from separate enantiomeric biosyntheses. A distinct feature of the biosynthesis of the cyclic pyrrole-imidazole dimers is the production of antipodal congeners without the corresponding enantiomers.

Funder

NIH

Welch Foundation

The University of Texas Southwestern Medical Center

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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