Asymmetric synthesis of 4,4-disubstituted-2-cyclohexen-1-ones from a chiral 2-(trimethylsilyl)benzamide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Thio-Claisen Rearrangements. An Asymmetric Synthesis of 4,4-Disubstituted Cyclohexenones with Vicinal Quaternary and Tertiary Stereocenters
2. Asymmetric Total Synthesis of (+)-Apovincamine and a Formal Synthesis of (+)-Vincamine. Demonstration of a Practical “Asymmetric Linkage” between Aromatic Carboxylic Acids and Chiral Acyclic Substrates
3. Solid-state photochemistry. Remarkable effects of the packing of molecules in crystals on the diastereoselectivity of the intramolecular 2 + 2 photocycloaddition of a 4-(3'-butenyl)-2,5-cyclohexadien-1-one
4. An improved procedure for the conversion of3,3-disubstituted-1,4-cyclohexadienes to 2,5-cyclohexadien-1-ones
5. Intramolecular 2 + 2 photocycloadditions of 4-(3'-alkenyl)- and 4-(3'-pentynyl)-2,5-cyclohexadien-1-ones
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4. ChemInform Abstract: Asymmetric Synthesis of 4,4-Disubstituted-2-cyclohexen-1-ones from a Chiral 2-(Trimethylsilyl)benzamide.;ChemInform;2010-08-03
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