Observations on the choice of Lewis acid and mode of addition for the Lewis acid mediated reaction of crotyltri- -butylstannane with aldehydes: convenient and highly selective access to both and products
- 1 January 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (36), 3927-3930
- https://doi.org/10.1016/0040-4039(84)80032-5
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Stereocontrolled additions of allyltri-Tetrahedron Letters, 1984
- Stereochemical consequences for the Lewis acid mediated additions of allyl and crotyltri-Tetrahedron Letters, 1984
- Chelation controlled diastereofacial selectivity in crotyltri--butylstannane additions to α-alkoxyaldehydesTetrahedron Letters, 1984
- Erythroselectivity in addition of γ-substituted allylsilanes to aldehydes in the presence of titanium chlorideTetrahedron Letters, 1983
- On the stereochemistry of allylmetal‐aldehyde condensations. Preliminary communicationHelvetica Chimica Acta, 1983
- Organometallic Compounds of Titanium and Zirconium as Selective Nucleophilic Reagents in Organic SynthesisAngewandte Chemie International Edition in English, 1983
- Diastereogenic Addition of Crotylmetal Compounds to AldehydesAngewandte Chemie International Edition in English, 1982
- Oraganometallic Compounds for Stereoregulated Synthesis of Acyclic Systems. Their Application to the Synthesis of the Prelog-Djerassi Lactonic AcidHETEROCYCLES, 1982
- Erythro-selective addition of crotyltrialkyltins to aldehydes regardless of the geometry of the crotyl unit. Stereoselection independent of the stereochemistry of precursorsJournal of the American Chemical Society, 1980