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Structural Revision of Lydiamycin A by Reinvestigation of the Stereochemistry

Cited 11 time in Web of Science Cited 11 time in Scopus
Authors

Hwang, Sunghoon; Shin, Daniel; Kim, Tae Ho; An, Joon Soo; Jo, Shin-Il; Jang, Jichan; Hong, Suckchang; Shin, Jongheon; Oh, Dong-Chan

Issue Date
2020-05
Publisher
American Chemical Society
Citation
Organic Letters, Vol.22 No.10, pp.3855-3859
Abstract
Lydiamycin A (1) is a previously reported piperazic acid-bearing cyclic peptide from Streptomyces. The absolute configuration of lydiamycin A has not been fully determined despite the fact that multiple total syntheses have been reported. The absolute configuration of 1 was reinvestigated by the advanced Marfey's method, chemical derivatization, and quantum-mechanics-based computational analysis, eventually resulting in a structural revision and establishment of the complete configuration. Lydiamycin A displayed weak antituberculosis activity in vitro.
ISSN
1523-7060
URI
https://hdl.handle.net/10371/202008
DOI
https://doi.org/10.1021/acs.orglett.0c01110
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  • College of Pharmacy
  • Department of Manufacturing Pharmacy
Research Area Development of methodologies using metal catalyst, Total synthesis of natural products

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