Synthesis of a Novel Macrolide: 9(S)-9-Dihydro-12-O-methylerythromycin A via Regioselective Methylation-Reference-Cited by-同舟云学术

Synthesis of a Novel Macrolide: 9(S)-9-Dihydro-12-O-methylerythromycin A via Regioselective Methylation

Published:1999-03-01 Issue:6 Volume:64 Page:2107-2109
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ku Yi-Yin¹,Riley David¹,Grieme Tim¹,Tien Jim¹,Zhang XiaoLin¹

Affiliation:

1. Chemical Process Research, Chemical and Agricultural Products Division, and Analytical Department, Pharmaceutical Products Division, Abbott Laboratories, North Chicago, Illinois 60064-4000

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9805605

Reference19 articles.

1. Erythromycin: A Microbial and Clinical Perspective After 30 Years of Clinical Use (First of Two Parts)

2. Erythromycin: A Microbial and Clinical Perspective After 30 Years of Clinical Use (Second of Two Parts)

3. Kurath, P.; Jones, P. H.; Egan, R. S.; Perun, T. J.Experientia1971,27, 362.

4. Kinetic studies on the decomposition of erythromycin A in aqueous acidic and neutral buffers

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2. Highlights of Semi-synthetic Developments from Erythromycin A;Current Pharmaceutical Design;2000-01-01

3. Synthesis and Antibacterial Activities of Novel 12-D-Methylerythromycin A Derivatives.;The Journal of Antibiotics;1999