Camphor-derived 2-stannyl-N-Boc-1,3-oxazolidine: A new chiral formylanion equivalent for the asymmetric synthesis of 1,2-diols
- 17 April 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (16) , 2863-2866
- https://doi.org/10.1016/0040-4039(95)00369-n
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Asymmetric synthesis of homochiral 1,2-diols via N-boc oxazolidinesTetrahedron Letters, 1994
- Chiral 2-lithio-13-dioxolanes and -2-lithiooxazolidines: New formyl anion equivalentsTetrahedron Letters, 1994
- .alpha.,.beta.-Unsaturated oxazolines, a powerful tool in asymmetric Diels-Alder cycloadditionsJournal of the American Chemical Society, 1990
- α-tributylstannylacetals: Preparation via transacetalisation of diethoxymethyltributyltin, and use for the synthesis of new α-stannylated ethersJournal of Organometallic Chemistry, 1990
- (Dialkoxymethyl)lithiums: generation, stability, and synthetic transformationsJournal of the American Chemical Society, 1989
- Asymmetric syntheses based on 1,3-oxathianes. 2. Synthesis of chiral tertiary .alpha.-hydroxy aldehydes, .alpha.-hydroxy acids, glycols [R1R2C(OH)CH2OH], and carbinols [R1R2C(OH)Me] in high enantiomeric purity.Journal of the American Chemical Society, 1984
- A Convenient Synthesis ofN,N-Disubstituted Aminomethyltri-n-butylstannanes, Precursors of the Corresponding Lithium ReagentsSynthesis, 1984
- Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketonesThe Journal of Organic Chemistry, 1983
- Quelques aspects de la reactivite de l'α-chloro α-ethoxymethyltributyletain : etherification reductrice des aldehydes aromatiques et mise en evidence de formyltributyletain lors de la reaction d'hydrolyseJournal of Organometallic Chemistry, 1983
- Asymmetric synthesis of nearly optically pure atrolactic acid methyl etherThe Journal of Organic Chemistry, 1979