Asymmetric Synthesis of Functionalized Secondary Alcohols by Catalytic Ring-Cleavage Reactions of Cyclic Acetals Derived from (R)-1,3-Butanediol
- 1 December 1996
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 69 (12) , 3639-3650
- https://doi.org/10.1246/bcsj.69.3639
Abstract
No abstract availableThis publication has 42 references indexed in Scilit:
- Highly diastereoselective acetal cleavages using novel reagents prepared from organoaluminum and pentafluorophenolJournal of the American Chemical Society, 1993
- Mechanism of the Lewis acid mediated cleavage of chiral acetalsThe Journal of Organic Chemistry, 1992
- On the stereoselectivity opening of achiral dioxane acetalsThe Journal of Organic Chemistry, 1991
- Studies on the mechanism and origin of stereoselective opening of chiral dioxane acetalsJournal of the American Chemical Society, 1991
- Chiral acetals in asymmetric synthesisTetrahedron: Asymmetry, 1990
- Acyclic stereoselection. 52. On the mechanism of Lewis acid mediated nucleophilic substitution reactions of acetalsThe Journal of Organic Chemistry, 1990
- Mechanistic and stereochemical divergence in the allylsilane-acetal addition reactionJournal of the American Chemical Society, 1989
- Asymmetric synthesis via acetal templates. 3. On the stereochemistry observed in the cyclization of chiral acetals of polyolefinic aldehydes; formation of optically active homoallylic alcoholsJournal of the American Chemical Society, 1983
- Practical asymmetric syntheses of 11-deoxydaunomycinone and related compoundsJournal of the American Chemical Society, 1982
- Practical asymmetric synthesis of aklavinoneJournal of the American Chemical Society, 1982