Unexpected Rearrangement in the Peroxytrifluoroacetic Acid-Mediated Baeyer-Villiger Oxidation of trans-3.beta.-Hydroxy-4,4,10.beta.-trimethyl-9-decalone Forming a 7-Oxabicyclo[2.2.1]heptane. Structure Proof and Total Synthesis of (.+-.)-Farnesiferol-C-Reference-Cited by-同舟云学术

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Unexpected Rearrangement in the Peroxytrifluoroacetic Acid-Mediated Baeyer-Villiger Oxidation of trans-3.beta.-Hydroxy-4,4,10.beta.-trimethyl-9-decalone Forming a 7-Oxabicyclo[2.2.1]heptane. Structure Proof and Total Synthesis of (.+-.)-Farnesiferol-C

Published:1995-08 Issue:16 Volume:60 Page:5114-5120
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Demnitz F. W. Joachim,Philippini Cristiane,Raphael Ralph A.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo00121a032

Cited by 27 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Stereospecific Nitrogen Insertion Using Amino Diphenylphosphinates: An Aza-Baeyer–Villiger Rearrangement;Organic Letters;2022-08-17

2. ε-Caprolactone manufacture via efficient coupling Baeyer-Villiger oxidation with aerobic oxidation of alcohols;Molecular Catalysis;2020-07

3. Diversity-Oriented Synthesis of Natural Products via Gold-Catalyzed Cascade Reactions;Synlett;2018-05-16

4. Construction of bicyclic systems containing an oxygen bridge by isomerization of cyclic epoxy alcohols;Tetrahedron Letters;2017-03

5. Regio- and Stereoselective Syntheses of 7-Oxabicyclo[2.2.1]heptanes via a Gold(I)-Catalyzed Cycloisomerization of Alkynediols: Asymmetric Total Synthesis of Farnesiferol C;Advanced Synthesis & Catalysis;2016-04-28

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