Rapid reduction of alkyl tosylates with lithium triethylborohydride. A convenient and advantageous procedure for the deoxygenation of simple and hindered alcohols. Comparison of various hydride reagents
- 15 August 1978
- journal article
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 156 (1) , 171-181
- https://doi.org/10.1016/s0022-328x(00)84874-3
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Selective reductive displacement of alkyl halides and sulfonate esters with cyanoborohydride reagents in hexamethylphosphoramideThe Journal of Organic Chemistry, 1977
- Reactions of lithium alkyl and alkynyl cuprates. Selective removal of halo and mesyloxy groups and reduction of .alpha.,.beta.-unsaturated ketonesJournal of the American Chemical Society, 1974
- Reductive removal of halo and mesyloxy groups with a copper(I) complexJournal of the American Chemical Society, 1973
- Sodium cyanoborohydride in hexamethylphosphoramide. An exceptionally selective reagent system for the reduction of alkyl iodides, bromides, and tosylatesJournal of the Chemical Society D: Chemical Communications, 1971
- Sodium borohydride in dimethyl sulfoxide or sulfolane. Convenient systems for selective reductions of primary, secondary and certain tertiary halides and tosylatesTetrahedron Letters, 1969
- Reduction of organic halogen compounds by sodium borohydrideThe Journal of Organic Chemistry, 1969
- A method for deoxygenation of allylic and benzylic alcoholsThe Journal of Organic Chemistry, 1969
- Selective Reductions. IX. Reaction of Lithium Aluminum Hydride with Selected Organic Compounds Containing Representative Functional Groups1Journal of the American Chemical Society, 1966
- Über Verbindungen mit Urotropin‐Struktur, XII. Monofunktionelle Adamantan‐DerivateEuropean Journal of Inorganic Chemistry, 1959
- 60. Triterpenoids. Part I. Morolic acid, a new triterpenoid sapogeninJournal of the Chemical Society, 1951