Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 3: Synthesis of Fragment C15-21-Reference-Cited by-同舟云学术

Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 3: Synthesis of Fragment C15-21

Published:2003-12-04 Issue:1 Volume:8 Page:107-112
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Mickel Stuart J.,Sedelmeier Gottfried H.,Niederer Daniel,Schuerch Friedrich,Koch Guido,Kuesters E.,Daeffler Robert,Osmani Adnan,Seeger-Weibel Manuela,Schmid E.,Hirni Alfred,Schaer Karl,Gamboni Remo,Bach Andrew,Chen Stephen,Chen Weichun,Geng Peng,Jagoe Christopher T.,Kinder Frederick R.,Lee George T.,McKenna Joseph,Ramsey Timothy M.,Repič Oljan,Rogers Larry,Shieh Wen-Chung,Wang Run-Ming,Waykole Liladhar

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op034132z

Reference8 articles.

1. Evolution of a Gram-Scale Synthesis of (+)-Discodermolide

2. Gram-Scale Synthesis of (+)-Discodermolide

3. Protection of hydroxy groups by intramolecular oxidative formation of methoxybenzylidene acetals with DDQ

4. Improved Procedure for the Reduction of N-Acyloxazolidinones

5. A new, economical, practical and racemization-free method for the reductive removal of 2-oxazolidinones from N-acyloxazolidinones with sodium borohydride

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