Syntheses and anti-MRSA activities of the C3 analogs of mansonone F, a potent anti-bacterial sesquiterpenoid: insights into its structural requirements for anti-MRSA activity-Reference-Cited by-同舟云学术

Syntheses and anti-MRSA activities of the C3 analogs of mansonone F, a potent anti-bacterial sesquiterpenoid: insights into its structural requirements for anti-MRSA activity

Published:2004-09 Issue:17 Volume:14 Page:4519-4523
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Shin Dong-Yun,Nam Kim Sun,Chae Jung-Hyun,Hyun Soon-Sil,Seo Seung-Yong,Lee Yong-Sil,Lee Kwang-Ok,Kim Seok-Ho,Lee Yun-Sang,Min Jeong Jae,Choi Nam-Song,Suh Young-Ger

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

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4. Oxazolidinone Structure–Activity Relationships Leading to Linezolid

5. Facile construction of the oxaphenalene skeleton by peri ring closure. Formal synthesis of mansonone F

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