Chemistry Letters p. 553 - 556 (1988)
Update date:2022-08-17
Topics:
Murakami, Teiichi
Harata, Kazuaki
Morimoto, Satoshi
Mono(3-acetylamino-3-deoxy)-β-cyclodextrin (4) was firstly prepared via regioselective ring opening of manno-epoxide by ammonia. 1H-NMR investigation clearly demonstrated that 4 recognized the chirality of mandelic acids and N-acetyl-phenyl-glycine by the formation of diastereomeric inclusion complexes.
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