Asymmetric synthesis of palitantin from the (5R)-tert-butyldimethylsiloxy-2-cyclohexenone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Efficient and practical synthesis of optically active 5-t-butyldimethylsiloxy-2-cyclohexenone as a convenient chiral 2,5-cyclohexadienone synthon
2. Unexpectedcis-Selective 1,4-Addition Reaction of Lower Order Cyanocuprates to Optically Active 5-(tert-Butyldimethylsiloxy)-2-cyclohexenone
3. Eine überraschendecis-selektive 1,4-Addition von Cyanocupraten niedriger Ordnung an optisch aktives 5-(tert-Butyldimethylsilyloxy)-2-cyclohexenon
4. Synthesis of Optically Active 5-(tert-Butyldimethylsiloxy)-2-cyclohexenone and Its 6-Substituted Derivatives as Useful Chiral Building Blocks for the Synthesis of Cyclohexane Rings. Syntheses of Carvone, Penienone, and Penihydrone
5. Studies in the biochemistry of micro-organisms
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3. Recent Advances on Stereoselective Organocatalytic Reactions. Organocatalytic Synthesis of Natural Products and Drugs;Catalytic Methods in Asymmetric Synthesis;2011-07-07
4. ChemInform Abstract: Asymmetric Synthesis of Palitantin from (5R)-tert-Butyldimethylsiloxy-2-cyclohexenone.;ChemInform;2010-06-11
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