Remote Allylic Silyloxy Groups as Stereocontrol Elements in Intramolecular Oxymercurations of γ-Hydroxyalkenes
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 61 (6) , 2109-2117
- https://doi.org/10.1021/jo951853q
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Syntheses of the Lower Portions of the Pamamycins from .gamma.-(Silyloxy)allenes Using Stereoselective Cyclization, Reduction, and Aldehyde Addition MethodologiesThe Journal of Organic Chemistry, 1994
- Substrate-directable chemical reactionsChemical Reviews, 1993
- Total synthesis of the polyether antibiotic ionomycinJournal of the American Chemical Society, 1990
- The total synthesis of (+)-ionomycinJournal of the American Chemical Society, 1990
- Bornane sultam-directed asymmetric synthesis of crystalline, enantiomerically pure syn aldolsJournal of the American Chemical Society, 1990
- The total synthesis of the polyether antibiotic X-206Journal of the American Chemical Society, 1988
- Modeling chemical reactivity. 7. The effect of a change in rate-limiting step on the stereoselectivity of electrophilic addition to allylic alcohols and related chiral alkenesJournal of the American Chemical Society, 1987
- Enantiodivergent syntheses of (+)- and (-)-nonactic acid and the total synthesis of nonactinJournal of the American Chemical Society, 1984
- A series of (2S)-2-O-protected-2-hydroxypropanals (L-lactaldehydes) suitable for use as optically active intermediatesThe Journal of Organic Chemistry, 1983
- Intramolecular .pi. coordination in .gamma.-phenylpropylmercurialsOrganometallics, 1982