Bicyclic Systems Related to Taxol. A Direct Means for Implementing C-2 Oxygenation and Demonstration of the Feasibility of α-Ketol Equilibration in a Fully Oxygenated B-Ring Setting-Reference-Cited by-同舟云学术

Bicyclic Systems Related to Taxol. A Direct Means for Implementing C-2 Oxygenation and Demonstration of the Feasibility of α-Ketol Equilibration in a Fully Oxygenated B-Ring Setting

Published:1998-01-01 Issue:1 Volume:63 Page:137-143
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Zeng Qingbei¹,Bailey Simon¹,Wang Ting-Zhong¹,Paquette Leo A.¹

Affiliation:

1. Evans Chemical Laboratories, The Ohio State University, Columbus, Ohio 43210

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo971592f

Reference14 articles.

1. ACS Symposium Series 583;For,1995

2. Generation of enantiopure trans-.DELTA.9,10-tricyclo[9.3.1.03,8]pentadecene diastereomers from a single precursor. Control of stereochemistry by means of rotationally restrictive nonbonded interactions

3. An unprecedented silyl triflate-promoted hydride shift within a taxane derivative

4. Setting the Bridgehead Oxidation Level intrans-Tricyclo[9.3.1.03,8]pentadecanes as a Prelude to the Dual Synthesis of Taxol and Taxusin

5. An Enantioselective Approach to the Taxanes: Direct access to functionalizedcis-tricyclo[9.3.1.03,8]pentadecanesvia ?-hydroxy ketone andWagner-Meerwein rearrangements

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