Domino Mukaiyama–Michael reactions in the synthesis of polycyclic systems
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference44 articles.
1. Stereoselective Mukaiyama-Michael/Michael/Aldol Domino Cyclization as the Key Step in the Synthesis of Pentasubstituted Arenes: An Efficient Access to Highly Active Inhibitors of Cholesteryl Ester Transfer Protein (CETP)
2. Double Michael addition reaction of oxophorone and its derivatives leading to bicyclo[2.2.2]octane compounds
3. Diastereoselective Approaches to trans-Hydrindane Derivatives − Total Synthesis of 8-(Phenylsulfonyl)de-A,B-cholestane Precursors to 25-Hydroxyvitamin D3
4. 1,3- versus 1,4-Asymmetric induction in Mukaiyama–Michael additions of optically active ketene acetals to 2-methylcyclopent-2-en-1-one: a remarkable inversion of facial selectivity
5. Tandem transformations initiated and determined by the Michael reaction
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