An Efficient Procedure for the Regioselective Monoprotection of 1,2-Diols
- 1 September 1992
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 48 (39) , 8337-8346
- https://doi.org/10.1016/s0040-4020(01)86582-0
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- A convenient procedure for the regioselective monoprotection of 1,n-diolsTetrahedron Letters, 1988
- Stereoselective reduction of bicyclic acetals. A method for reductive generation of heterocyclic ring systemsTetrahedron Letters, 1987
- Reductive cleavages of homochiral acetals: inversion of the stereoselectivityTetrahedron, 1987
- Regioselective manipulation of hydroxyl groups via organotin derivativesTetrahedron, 1985
- The brominolysis reaction of stannylene derivatives: a regiospecific synthesis of carbohydrate-derived hydroxy-ketonesJournal of the Chemical Society, Perkin Transactions 1, 1979
- An efficient reduction of acetals and ketals to methyl ethers.Tetrahedron Letters, 1978
- Stereoselective ring-cleavage of 3-O-benzyl- and 2,3-di-O-benzyl-4,6-O-benzylidenehexopyranoside derivatives with the LiAlH4AlCl3, reagentCarbohydrate Research, 1975
- Reductive Cleavage of Acetals and Ketals by BoraneCanadian Journal of Chemistry, 1974
- Reaction of O-benzylidene sugars with N-bromosuccinimide. II. Scope and synthetic utility in the methyl 4,6-0-benzylidenehexopyranoside seriesThe Journal of Organic Chemistry, 1969
- Reduction with Metal Hydrides. XII. Reduction of Acetals and Ketals with Lithium Aluminum Hydride-Aluminum ChlorideJournal of the American Chemical Society, 1962