A novel and convenient route to cyclic and acyclic carbonates from unprotected methyl d-glycosides
- 10 June 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (24) , 2751-2754
- https://doi.org/10.1016/0040-4039(91)85076-h
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- A new protected form of glucuronic acid for the synthesis of labile 1-O-acyl-β-D-glucuronidesTetrahedron Letters, 1989
- Glycosylations de Diols-4,6 en SerieGlucoetManno, Utilises Comme Accepteurs, Avec des DonneursN-Allyloxycarbonyles de la GlucosamineJournal of Carbohydrate Chemistry, 1989
- Selective cleavage of the allyl and (allyloxy)carbonyl groups through palladium-catalyzed hydrostannolysis with tributyltin hydride. Application to the selective protection-deprotection of amino acid derivatives and in peptide synthesisThe Journal of Organic Chemistry, 1987
- Use of the Allyloxycarbonyl Protective Group in Carbohydrate ChemistryJournal of Carbohydrate Chemistry, 1986
- Total synthesis of bleomycin A21)Tetrahedron Letters, 1982
- Practical synthesis of O-β-d-mannopyranosyl-, O-α-d-mannopyranosyl-, and O-β-d-glucopyranosyl-(1→4)-O-α-l-rhamnopyranosyl-(1→3)-d-galactosesCarbohydrate Research, 1980
- Regioselective syntheses of mono-O-acylglucoses.CHEMICAL & PHARMACEUTICAL BULLETIN, 1979
- Use of 2,2,2-tribromoethyl chloroformate for the protection of nucleoside hydroxyl groupsThe Journal of Organic Chemistry, 1968
- A facile route to trans cyclic carbonates of sugarsCarbohydrate Research, 1967
- Use of p-nitrophenyl chloroformate in blocking hydroxyl groups in nucleosidesThe Journal of Organic Chemistry, 1967