Highly stereoselective approach to chiral building block possessing three contiguous asymmetric centers. Preparation of four possible diastereomers of β,β′-dimethyl-bis-homoallylic alcohol derivative
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (31) , 3707-3710
- https://doi.org/10.1016/s0040-4039(00)89229-1
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Enantio- and diastereomerically pure threo-homoallylic alcohols via highly stereoselective reduction of α-methyl-β,γ-unsaturated ketonesTetrahedron Letters, 1984
- Asymmetric synthesis of optically pure α-methyl-β,γ-unsaturated ketones via triethylaluminum-mediated stereospecific pinacol rearrangement of alkenyl groupsTetrahedron Letters, 1984
- Reductive pinacol-type rearrangement of chiral α-mesyloxy ketones promoted by organoaluminum compoundsTetrahedron Letters, 1984
- Synthesis of four possible steric isomers of β-methylhomoallyl alcoholsJournal of the Chemical Society, Chemical Communications, 1984
- Stereoselective synthesis of the synthons having three consective chiral centersTetrahedron Letters, 1983
- Stereocontrolled synthesis of chiral synthons for polyketide-derived natural productsTetrahedron Letters, 1983
- Stereoselective reactions of chiral enolates. Application to the synthesis of (+)-prelog-djerassi lactonic acid.Tetrahedron Letters, 1982
- Total synthesis of 6-deoxyerythronolide BJournal of the American Chemical Society, 1981
- Further synthetic studies on rifamycin sTetrahedron, 1981
- Stereo- and regioselective methods for the synthesis of three consecutive asymmetric units found in many natural productsTetrahedron Letters, 1979