Preparation of Alkyl Silyl Acetals from Carboxylic Esters with tert-Butyldimethylsilyldihalomethyllithium. 1,3-Rearrangement of Silyl Group from Carbon to Oxygen
- 1 June 1995
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 24 (6) , 461-462
- https://doi.org/10.1246/cl.1995.461
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Evidence for an Oxocarbenium Ion Intermediate in Lewis Acid Mediated Reactions of Acyclic AcetalsJournal of the American Chemical Society, 1994
- tert-Butyldimethylsilyldichloromethyllithium as a dichloromethylene dianion synthon. 1,3-rearrangement of silyl group from carbon to oxideTetrahedron Letters, 1993
- First general synthesis of monosilyl acetals. Trimethylsilyl trapping of the intermediate in DIBALH reduction of carboxylic acid esters using trimethylsilyl trifluoromethanesulfonateTetrahedron Letters, 1993
- Highly selective acetal cleavage using new organoaluminum reagentsJournal of the American Chemical Society, 1991
- Asymmetric synthesis via acetal templates. 3. On the stereochemistry observed in the cyclization of chiral acetals of polyolefinic aldehydes; formation of optically active homoallylic alcoholsJournal of the American Chemical Society, 1983