Grignard reagent induced tandem semipinacol rearrangement/ketone addition reaction of 20S-hydroxy-5α-pregnane-16(17)-epoxide-Reference-Cited by-同舟云学术

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Grignard reagent induced tandem semipinacol rearrangement/ketone addition reaction of 20S-hydroxy-5α-pregnane-16(17)-epoxide

Published:2011-08 Issue:32 Volume:52 Page:4123-4125
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Huang Chun-Xi,Shi Yong,Lin Jing-Rong,Jin Rong-Hua,Tian Wei-Sheng

Funder

Science and Technology Commission of Shanghai Municipality

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. Recent advances in the semi-pinacol rearrangement of α-hydroxy epoxides and related compounds

2. A Tandem Non-Aldol Aldol Mukaiyama Aldol Reaction

3. Samarium-Catalyzed Tandem Semipinacol Rearrangement/Tishchenko Reaction ofα-Hydroxy Epoxides: A Novel Approach to Highly Stereoselective Construction of 2-Quaternary 1,3-Diol Units

4. Stereoselective Reductive Rearrangement of α-Hydroxy Epoxides: A New Method for Synthesis of 1,3-Diols1

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1. Microbial metabolism of diosgenin by a novel isolated Mycolicibacterium sp. HK‐90: A promising biosynthetic platform to produce 19‐carbon and 21‐carbon steroids;Microbial Biotechnology;2024-02

2. The Semipinacol Rearrangements;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2023

3. A Tandem Semipinacol Rearrangement/Aldehyde Arylation or Alkylation of Trisubstituted 2,3-Epoxy Alcohols with Grignard Reagents for Functionalized 1,3-Diols;The Journal of Organic Chemistry;2022-06-09

4. Ring Opening Reactions of Epoxides. A Review;Organic Preparations and Procedures International;2021-11-08

5. A one-pot diastereoselective synthesis of 1,3-diols and 1,3,5-triols via cascade reactions of arylalkynyl Grignard reagents with enol esters;Journal of Chemical Research;2020-03-04

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