期刊
ORGANIC LETTERS
卷 11, 期 9, 页码 1983-1985出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol900413s
关键词
-
资金
- Lundbeck Foundation
A method for selective monofunctionalition of readily available cyclodextrin diols (2(A-F),3(A-F),6(B,C,E,F)-hexadeca-O-benzyl-alpha-cyclodextrin and 2(A-G),3(A-G),6(B,C,E-G)-nonadeca-O-benzyl-beta-cyclodextrin) by regioselective nucleophilic opening of their cyclic sulfates is presented. Although the A and D products are nonequivalent in beta-cyclodextrin, only the A product is formed.
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