One-step stereospecific conversion of alcohols into dithiocarbamates: A smooth pathway for the introduction of a sulphur functionality
- 31 December 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (35) , 4169-4170
- https://doi.org/10.1016/s0040-4039(00)84938-2
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Nucleophilic Inversions of a Chiral Alcohol Mediated by Zinc SaltsSynthetic Communications, 1986
- Pentadienyl dithiocarbamate as a 1,5-dianion equivalent. Versatile reagent for polyene synthesisJournal of the American Chemical Society, 1983
- A novel, reductive ring-opening of carbohydrate benzylidene acetals, with unusual regioselectivityCarbohydrate Research, 1981
- Synthèse du 4-O-[(s)-1-carboxyéthyl]-d-glucose et de son isomère (R)Carbohydrate Research, 1978
- NEW SYNTHETIC REACTIONS BASED ON 1-METHYL-2-FLUOROPYRIDINIUM SALTS. STEREOSPECIFIC PREPARATION OF THIOALCOHOLS FROM ALCOHOLSChemistry Letters, 1977
- Stereoselective ring-cleavage of 3-O-benzyl- and 2,3-di-O-benzyl-4,6-O-benzylidenehexopyranoside derivatives with the LiAlH4AlCl3, reagentCarbohydrate Research, 1975
- Syntheses of ThiocarbamatesAngewandte Chemie International Edition in English, 1967
- Thiousugars.X.Studies on Glycosyl N, N-DialkyldithiocarbamatesCHEMICAL & PHARMACEUTICAL BULLETIN, 1967