Stereocontrol in intramolecular Michael–aldol reaction sequences of 3-acetoacetoxycholest-4-en-6-ones
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1994/P1/P19940000913
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1. Pentacyclic steroids. Part 1. Synthesis and X-ray conformational analysis of 4α,5β- and 4α,5β-dihydrobenzo[4,5,6]cholestan-5′(6′H)-one
2. Conformational analysis of tricyclo[7.3.1.05,13]tridecane (perhydrophenalene) by molecular mechanics
3. Synthesis of a potential forskolin A-B ring precursor by tandem Michael-Aldol reactions
4. Intramolecular Michael-aldol condensation approach to the construction of advanced intermediates in the synthesis of forskolin
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1. ChemInform Abstract: Stereocontrol in Intramolecular Michael-Aldol Reaction Sequences of 3- Acetoacetoxycholest-4-en-6-ones.;ChemInform;2010-08-19
2. Stereocontrol in a one-pot procedure for anionic oxy-Cope rearrangement followed by intramolecular aldol reaction;Journal of the Chemical Society, Perkin Transactions 1;2001
3. The Michael-Aldol Condensation Approach to the Construction of Key Intermediates in the Synthesis of Nimbolide and Nagilactone A;Synthetic Communications;1996-07
4. Steroids: reactions and partial synthesis;Natural Product Reports;1996
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