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Concise and practical approach to chiral des-A B-trienic corticosteroids

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TLDR
In this article, a concise and practical route to the enantiomerically pure des-A B-trienic steroid was developed by thermolysis of the optically active alkenic benzocyclobutene 13 obtained by selective nucleophilic addition of isopropenyl group to the chiral epoxide 9 as a key step.
Abstract
A concise and practical route to the enantiomerically pure des-A B-trienic steroid 14 was developed by thermolysis of the optically active alkenic benzocyclobutene 13 obtained by selective nucleophilic addition of isopropenyl group to the chiral epoxide 9 as a key step.

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Citations
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Journal ArticleDOI

Recent chemistry of benzocyclobutenes

TL;DR: In this article, a review of aspects related to the synthesis, reactions and applications of benzocyclobutenes is presented, including reactions, reactions, and applications, as well as the synthesis process.
Journal ArticleDOI

Cycloadditions of ortho-quinodimethanes derived from benzocyclobutenes in organic synthesis. a review

TL;DR: In this paper, the authors describe the CYCLOADDITIONS OF ortho-quinodimETHANES DERIVED FROM BENZOCYCLOBUTENES in ORGANIC SYNTHESIS.
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Ring C closure as key step in the synthesis of steriods

TL;DR: In this paper, the authors reviewed the use of Torgov syntheses, Michael additions and cyclisations, aldol cyclisation, polyene cyclisations and Friedel-Crafts cyclisations for the construction of Ring C.
References
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Journal ArticleDOI

Horner-wadsworth-emmons reaction: Use of lithium chloride and an amine for base-sensitive compounds

TL;DR: A mild olefination procedure, utilizing LiCl and an amine, has been developed for use with base-sensitive aldehydes and phosphonates as discussed by the authors.
Journal ArticleDOI

The synthetic methodology of nonracemic glycidol and related 2,3-epoxy alcohols

Robert M. Hanson
- 01 Jun 1991 - 
TL;DR: Berch et al. as mentioned in this paper presented a Synthetic Methodology of Nonra cemic Glycidol and Related 2,3-Epoxy Alcohols, Chemi cal Reviews, vol. 91, No. 4, (Jun. 1991) pp. 437-475.
Journal ArticleDOI

Regio- and stereoselective ring opening of epoxy alcohols with organoaluminium compounds leading to 1,2-diols

TL;DR: In this paper, the introduction of alkyl, alkynyl group, or hydride occurs regioselectively at the 3 position of the epoxy alcohols with inversion of the configuration upon treatment with organoaluminium reagents to produce vic-diols.