Crossref journal-article
Oxford University Press (OUP)
Chemistry Letters (286)
Abstract

Abstract 1,2-cis-Ribofuranosides are stereoselectively synthesized in high yields by the reaction of β-ribofuranosyl fluoride and alcohols in the presence of stannous chloride and trityl perchlorate. Under similar condition, α-arabinofuranosyl fluoride reacts with cholestanol to give 1,2-cis-arabinofuranoside predominatly.

Bibliography

Mukaiyama, T., Hashimoto, Y., & Shoda, S. (1983). STEREOSELECTIVE SYNTHESIS OF 1,2-CIS-GLYCOFURANOSIDES USING GLYCOFURANOSYL FLUORIDES. Chemistry Letters, 12(6), 935–938.

Dates
Type When
Created 19 years, 1 month ago (July 24, 2006, 10:44 p.m.)
Deposited 1 year, 7 months ago (Jan. 19, 2024, 12:53 p.m.)
Indexed 9 months, 2 weeks ago (Nov. 19, 2024, 11 a.m.)
Issued 42 years, 3 months ago (June 1, 1983)
Published 42 years, 3 months ago (June 1, 1983)
Published Online 19 years, 5 months ago (March 27, 2006)
Published Print 42 years, 2 months ago (June 5, 1983)
Funders 0

None

@article{Mukaiyama_1983, title={STEREOSELECTIVE SYNTHESIS OF 1,2-CIS-GLYCOFURANOSIDES USING GLYCOFURANOSYL FLUORIDES}, volume={12}, ISSN={1348-0715}, url={http://dx.doi.org/10.1246/cl.1983.935}, DOI={10.1246/cl.1983.935}, number={6}, journal={Chemistry Letters}, publisher={Oxford University Press (OUP)}, author={Mukaiyama, Teruaki and Hashimoto, Yukihiko and Shoda, Shin-ichiro}, year={1983}, month=jun, pages={935–938} }