Deciphering Piperidine Formation in Polyketide-Derived Indolizidines Reveals a Thioester Reduction, Transamination, and Unusual Imine Reduction Process-Reference-Cited by-同舟云学术

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Deciphering Piperidine Formation in Polyketide-Derived Indolizidines Reveals a Thioester Reduction, Transamination, and Unusual Imine Reduction Process

Published:2016-11-03 Issue:12 Volume:11 Page:3278-3283
ISSN:1554-8929
Container-title:ACS Chemical Biology
language:en
Short-container-title:ACS Chem. Biol.

Author:

Peng Haidong¹,Wei Erman¹,Wang Jiali¹,Zhang Yanan¹,Cheng Lin¹,Ma Hongmin¹,Deng Zixin¹,Qu Xudong¹²

Affiliation:

1. Key Laboratory of Combinatorial Biosynthesis and Drug Discovery Ministry of Education, School of Pharmaceutical Sciences, Wuhan University, 185 Donghu Road, Wuhan 430071, China

2. Jiangsu National Synergetic Innovation Center for Advanced Materials (SICAM), 200 North Zhongshan Road, Nanjing 210009, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Molecular Medicine,General Medicine,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acschembio.6b00875

Reference28 articles.

1. Medicinal Natural Products

2. Bioactive Microbial Metabolites

3. Pyrrole, pyrrolidine, pyridine, piperidine and tropane alkaloids (1998 to 1999)

4. Indolizidine and quinolizidine alkaloids

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