Carboxyl Formation from Methyl via Triple Hydroxylations by XiaM in Xiamycin A Biosynthesis-Reference-Cited by-同舟云学术

Carboxyl Formation from Methyl via Triple Hydroxylations by XiaM in Xiamycin A Biosynthesis

Published:2012-12-03 Issue:24 Volume:14 Page:6142-6145
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhang Qingbo¹,Li Huixian¹,Li Sumei¹,Zhu Yiguang¹,Zhang Guangtao¹,Zhang Haibo¹,Zhang Wenjun¹,Shi Rong¹,Zhang Changsheng¹

Affiliation:

1. CAS Key Laboratory of Marine Bio-resources Sustainable Utilization, RNAM Center for Marine Microbiology, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, Chinese Academy of Sciences, 164 West Xingang Road, Guangzhou 510301, China, Graduate University of the Chinese Academy of Sciences, Beijing 100049, China, and Département de Biochimie, de Microbiologie et de Bio-informatique, PROTEO et IBIS, Université Laval, Québec, G1V 0A6, Canada

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol302782u

Reference24 articles.

1. Oridamycins A and B, Anti-Saprolegnia parasitica Indolosesquiterpenes Isolated from Streptomyces sp. KS84

2. Xiamycin, a pentacyclic indolosesquiterpene with selective anti-HIV activity from a bacterial mangrove endophyte

3. A family of multicyclic indolosesquiterpenes from a bacterial endophyte

4. N-N-Coupled Indolo-sesquiterpene Atropo-Diastereomers from a Marine-Derived Actinomycete

5. Identification and Characterization of Xiamycin A and Oxiamycin Gene Cluster Reveals an Oxidative Cyclization Strategy Tailoring Indolosesquiterpene Biosynthesis

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