Remarkable increase in the diastereofacial selectivity of the addition of β-methyl α-(alkoxy)allylstannane to aldehydes: substituent effects on diastereofacial selectivity
- 1 January 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (1) , 13-16
- https://doi.org/10.1016/s0040-4039(00)71205-6
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Total synthesis of FK506 and an FKBP probe reagent, [C(8),C(9)-13C2]-FK506Journal of the American Chemical Society, 1990
- Total synthesis of (+)-colletodiol: new methodology for the synthesis of macrolactonesThe Journal of Organic Chemistry, 1989
- Cobalt(II) chloride-promoted thionation of carbonyl compounds: a simple access to silyl thio ketones and thio aldehydesThe Journal of Organic Chemistry, 1989
- Synthesis of homochiral α-alkoxystannanes: stereospecific conversion to cembranolide precursorsTetrahedron Letters, 1988
- Stereoselective total synthesis of cembranolides through cyclizationof a homochiral (α-alkoxyallyl)stannane precursorTetrahedron Letters, 1988
- Acyclic stereocontrol via allylic organometallic compoundsAccounts of Chemical Research, 1987
- Highly stereoselective reaction ofα-methylthio aldehydes with allyltriphenylstannane: Synthesis of anti-β-methylthio alcoholsTetrahedron Letters, 1985
- Stereocontrolled additions of allyltri-Tetrahedron Letters, 1984
- Stereo- and regiocontrol of acyclic systems via the lewis acid mediated reaction of allylic stannanes with aldehydesTetrahedron, 1984
- Chelation controlled diastereofacial selectivity in crotyltri--butylstannane additions to α-alkoxyaldehydesTetrahedron Letters, 1984