期刊
ORGANIC LETTERS
卷 19, 期 17, 页码 4516-4519出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b02080
关键词
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资金
- National Science Foundation [CHE-1362213]
- Joan and Marvin Carmack Chair funds
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [1362213] Funding Source: National Science Foundation
S-Propyl glycosides of less activated sugars, such as peracetylated carbohydrates and uronic acid esters that could not previously be activated with triphenylbismuth ditriflate alone, were found to be glycosylated in the presence of propanethiol as an additive in under 3 h. This newly developed protocol was also found to be effective in promoting glycosylation of neutral and uronic acid esters of S-phenyl, S-thiazolinyl, S-benzoxazolyl, and S-adamantyl glycosides as well as sialic acid.
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