Fleming−Tamao Oxidation and Masked Hydroxyl Functionality: Total Synthesis of (+)-Pramanicin and Structural Elucidation of the Antifungal Natural Product (−)-Pramanicin-Reference-Cited by-同舟云学术

Fleming−Tamao Oxidation and Masked Hydroxyl Functionality: Total Synthesis of (+)-Pramanicin and Structural Elucidation of the Antifungal Natural Product (−)-Pramanicin

Published:1999-07-23 Issue:16 Volume:64 Page:6005-6018
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Barrett Anthony G. M.¹,Head John¹,Smith Marie L.¹,Stock Nicholas S.¹,White A. J. P.¹,Williams D. J.¹

Affiliation:

1. Department of Chemistry, Imperial College of Science, Technology and Medicine, South Kensington, London SW7 2AZ, United Kingdom, and Celltech Therapeutics, 216 Bath Road, Slough, Berkshire SL1 4EN, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9905672

Reference34 articles.

1. Pramanicin, a novel antimicrobial agent from a fungal fermentation

2. The biosynthesis of pramanicin: origin of the carbon skeleton

3. Approaches to the Synthesis of Cytochalasans Part9. A versatile concept leading to all structural types of cytochalasans

4. The Utility of Phosphonate Carbanions in Olefin Synthesis

5. A useful 12-I-5 triacetoxyperiodinane (the Dess-Martin periodinane) for the selective oxidation of primary or secondary alcohols and a variety of related 12-I-5 species

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