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.
References
13
Referenced
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{'key': '2024011917524269700_r8'}
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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) |
@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} }