Hydroxylamine-Mediated Anthrapyranone Formation, Solving 5-exo/6-endo Issue toward Synthesis of Pluramycin-Class Antibiotics-Reference-Cited by-同舟云学术

Hydroxylamine-Mediated Anthrapyranone Formation, Solving 5-exo/6-endo Issue toward Synthesis of Pluramycin-Class Antibiotics

Published:2019-12-16 Issue:1 Volume:22 Page:175-179
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Shimura Jun¹,Ando Yoshio¹^ORCID,Suzuki Keisuke¹^ORCID

Affiliation:

1. Department of Chemistry, Tokyo Institute of Technology, 2-12-1 O-okayama, Meguro-ku, Tokyo 152-8551, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b04127

Reference60 articles.

1. bSéquin, U. In Progress in the Chemistry of Organic Natural Products; Herz, W.; Grisebach, H.; Kirby, G. W.; Tamm, C., Eds. Springer: New York, 1986; pp 57–122.

2. cNote that the relative stereochemistry of the epoxide in pluramycin A has not been determined.

3. Pluramycins. Old Drugs Having Modern Friends in Structural Biology

4. Altromycin B Threads the DNA Helix Interacting with Both the Major and the Minor Grooves To Position Itself for Site-Directed Alkylation and Guanine N7

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