Simple and Practical Routes to Enantiomerically Pure 5-(Trialkylsilyl)-2-cyclohexenones
- 4 August 1999
- journal article
- letter
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 1 (5) , 811-814
- https://doi.org/10.1021/ol990805f
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Lipase-mediated diastereoselective and enantioselective acetylations of 3-substituted cyclohexanolsTetrahedron Letters, 1998
- A simple, effective, new, palladium-catalyzed conversion of enol silanes to enones and enalsTetrahedron Letters, 1995
- The phenyldimethylsilyl group as a masked hydroxy groupJournal of the Chemical Society, Perkin Transactions 1, 1995
- Conjugate addition of the phenyldimethylsilyl group to αβ-unsaturated carbonyl compounds using a silylzincate in place of the silylcuprateJournal of the Chemical Society, Perkin Transactions 1, 1994
- Enantiodivergent Preparation of Chiral 2,5-Cyclohexadienone SynthonsSynthesis, 1993
- The first isolation of lignans, megacerotonic acid and anthocerotonic acid, from non-vascular plants, anthocerotae (hornworts)Tetrahedron Letters, 1990
- Synthesis of (R)-(+)-4-Butyl-2,6-cycloheptadienone, a Constituent of Marine AlgaeChemistry Letters, 1988
- Synthesis of chiral 5-substituted cyclohex-2-enones from 5-trimethylsilylcyclohex-2-enoneJournal of the Chemical Society, Chemical Communications, 1988
- Highly selective, kinetically controlled enolate formation using lithium dialkylamides in the presence of trimethylchlorosilaneTetrahedron Letters, 1984
- Dimethyloxosulfonium Methylide ((CH3)2SOCH2) and Dimethylsulfonium Methylide ((CH3)2SCH2). Formation and Application to Organic SynthesisJournal of the American Chemical Society, 1965