A new stereoselective method for synthesis of optically active β-alkylhomoallyl alcohols and γ,δ-epoxy-β-alkyl alcohols
- 14 January 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (3) , 371-374
- https://doi.org/10.1016/s0040-4039(00)92631-5
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Synthesis of optically active α-trimethylsilyl δα,β-butenolides and their conversion into various butenolides and saturated γ-lactonesTetrahedron Letters, 1990
- Asymmetric synthesis using tartrate ester modified allylboronates. 1. Factors influencing stereoselectivityThe Journal of Organic Chemistry, 1990
- Practical method for synthesis of optically pure propargylic alcoholsTetrahedron Letters, 1989
- An efficient synthesis of 2(5H)-furanone and furan derivatives using 3-(phenylthio)propenal as a 1,3-dipolar synthon.CHEMICAL & PHARMACEUTICAL BULLETIN, 1989
- A highly efficient synthesis of optically pure γ-iodo allylic alcohols and their conversion into various optically active allylic alcoholsTetrahedron Letters, 1987
- [2,3]-Wittig sigmatropic rearrangements in organic synthesisChemical Reviews, 1986
- Diastereo- and enantioselective preparation of β-alkylhomoallylic alcoholsTetrahedron, 1986
- Acyclic stereoselection using highly stereoselective addition reaction of achiral nucleophiles to chiral carbonyl compounds.Journal of Synthetic Organic Chemistry, Japan, 1986
- Stereoselective synthesis of .gamma.,.delta.-epoxy-.beta.-methyl-.gamma.-(trimethylsilyl)alkanols. Synthesis of the C(1)-C(7) segment of 6-deoxyerythronolide BJournal of the American Chemical Society, 1985
- Vanadium-catalyzed epoxidations. 2. Highly stereoselective epoxidations of acyclic homoallylic alcohols predicted by a detailed transition-state modelJournal of the American Chemical Society, 1981