N-Acetylbornane-10,2-sultam: A Useful, Enantiomerically Pure Acetate Synthon for Asymmetric Aldol Reactions
- 1 September 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 62 (18) , 6397-6400
- https://doi.org/10.1021/jo961953b
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- The total synthesis of pamamycin 607. 1. Synthesis of a C1′-C11′ synthonTetrahedron Letters, 1996
- Remote Allylic Silyloxy Groups as Stereocontrol Elements in Intramolecular Oxymercurations of γ-HydroxyalkenesThe Journal of Organic Chemistry, 1996
- Efficient asymmetric synthesis of anti-aldols from bornanesultam derived boryl enolatesTetrahedron Letters, 1993
- Optically pure, crystalline ‘acetate’-aldols from N-acetylbornane-10,2-sultamTetrahedron Letters, 1992
- Synthesis of 3-pyrrolines by an intramolecular Wittig reactionThe Journal of Organic Chemistry, 1991
- Transition-state modeling of the aldol reaction of boron enolates: a force field approachThe Journal of Organic Chemistry, 1990
- Theoretical studies of aldol stereoselectivity: the development of a force field model for enol borinates and the investigation of chiral enolate .pi.-face selectivityThe Journal of Organic Chemistry, 1990
- Bornane sultam-directed asymmetric synthesis of crystalline, enantiomerically pure syn aldolsJournal of the American Chemical Society, 1990
- Metal ion effects in Wittig reactions. A general hypothesis for the mechanism of the Wittig reactionThe Journal of Organic Chemistry, 1990
- Enantio‐ and anti‐Diastereoselective Aldol Additions of Acetates and Propionates via O‐Silyl Ketene AcetalsAngewandte Chemie International Edition in English, 1985