Neighbouring group participation in the cleavage of steroidal α-hydroxyacetals
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1992/P1/P19920000075
Reference28 articles.
1. Rearrangement of a steroidal α-hydroxyacetal: a convenient new method for the introduction of a 5α-methyl group into the steroid nucleus
2. The Grignard addition to steroidal cyclic ketals
3. THE STEREOCHEMISTRY OF THE i-STEROIDS AND THEIR TRANSFORMATION PRODUCTS
4. Nitration of Unsaturated Steroids
5. Nonenzymic biogenetic-like olefinic cyclizations. Stereospecific cyclization of dienic acetals
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1. Westphalen Rearrangement;Comprehensive Organic Name Reactions and Reagents;2010-09-15
2. ChemInform Abstract: Neighboring Group Participation in the Cleavage of Steroidal α- Hydroxyacetals.;ChemInform;2010-08-22
3. Steroids: reactions and partial syntheses;Natural Product Reports;1994
4. Cleavage of steroidal α-hydroxy acetals with methylmagnesium iodide;J. Chem. Soc., Perkin Trans. 1;1993
5. Steroids;The Chemistry of Natural Products;1993
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