Effect of 9,10-Cyclic Acetal Stereochemistry on Feasible Operation of the α-Ketol Rearrangement in Highly Functionalized Paclitaxel (Taxol) Precursors-Reference-Cited by-同舟云学术

Effect of 9,10-Cyclic Acetal Stereochemistry on Feasible Operation of the α-Ketol Rearrangement in Highly Functionalized Paclitaxel (Taxol) Precursors

Published:2003-02-19 Issue:6 Volume:68 Page:2266-2275
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Paquette Leo A.¹,Hofferberth John E.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/jo020627v

Reference35 articles.

1. Enantiospecific Total Synthesis of Natural (+)-Taxusin. 1. Retrosynthesis, Advancement to Diastereomeric trans-Δ9,10-Tricyclic Olefinic Intermediates, and the Stereocontrol Attainable Because of Intrinsic Rotational Barriers Therein

2. Enantiospecific Total Synthesis of Natural (+)-Taxusin. 2. Functionalization of the A-Ring and Arrival at the Target

3. From D-camphor to the taxanes. Highly concise rearrangement-based approaches to taxusin and taxol

4. Recent applications of anionic oxy-cope rearrangements

5. Stereocontrolled Construction of Complex Cyclic Ketones via Oxy-Cope Rearrangement

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