Reactions of 2,3,5-Tri-O-benzoyl-d-ribofuranosyl Acetate with Enol Silyl Ethers Catalyzed by Tin(IV) Chloride. Regiochemical Features
- 1 February 1984
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 57 (2) , 553-556
- https://doi.org/10.1246/bcsj.57.553
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Regiochemical aspects in the reaction of 2,3,5-tri-o-benzoyl-d-ribofuranosylTetrahedron Letters, 1982
- Chirally selective synthesis of sugar moiety of nucleosides by chemicoenzymatic approach: L- and D-riboses, showdomycin, and cordycepinJournal of the American Chemical Society, 1981
- Total synthesis of the C-nucleoside dl-showdomycin by a Diels-Alder, retrograde Dieckmann strategyJournal of the American Chemical Society, 1981
- A general stereocontrolled route to carbocyclic C-nucleosides: (±) carba-showdowmycinTetrahedron Letters, 1981
- A stereocontrolled general synthesis of C-nucleosidesJournal of the American Chemical Society, 1978
- C-Nucleosides and related compounds. VII. Synthesis of carbocyclic analogues of C-nucleosidesCanadian Journal of Chemistry, 1976
- 5 The Chemistry and Biochemistry of C-NucleosidesProgress in Medicinal Chemistry, 1976
- Synthesis of the pyrazomycinsThe Journal of Organic Chemistry, 1976
- C-Glycosyl nucleosides. IV. Synthesis of several 4-(.beta.-D-ribofuranosyl)pyrazolesThe Journal of Organic Chemistry, 1974
- C-Glycosyl nucleosides. III. Facile synthesis of the nucleoside antibiotic showdomycinThe Journal of Organic Chemistry, 1973