Tetrahedron Letters p. 3587 - 3590 (1984)
Update date:2022-08-03
Topics:
Fujita, Kahee
Ejima, Seiji
Imoto, Taiji
Cyclohexaamylose hydrolyzed α-naphthyl acetates more rapidly than the corresponding β-isomers, a phenomenon termed "α-selectivity", while cyclopentaamylose showed 'β-selectivity' and the selectivity of cycloheptaamylose fell between those of cyclohexa- and cycloocta-amyloses.
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Doi:10.1246/bcsj.35.1869
(1962)Doi:10.1080/10426500500543768
(2006)Doi:10.1007/s00706-013-1123-3
(2014)Doi:10.1002/jps.2600730837
(1984)Doi:10.1002/ejic.200600241
(2006)Doi:10.1016/S0040-4020(01)83511-0
(1984)
