Enantiomeric excesses of several alcohols and an amine have been determined by derivatization with racemic 2'-methoxy-1,1'-binaphthyl-2-carbonyl chloride rac-1, with no requirement for kinetic resolution in the acylation step. The necessary information is provided instead by CD and UV spectra of the derived esters and amides, the chiral signal being dominated by the binaphthyl component. (C) 2001 Elsevier Science Ltd. All rights reserved.
机构:Hokkaido Univ, Fac Agr, Dept Appl Biosci, Kita Ku, Sapporo, Hokkaido 0608589, Japan
Fukui, H
Fukushi, Y
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Hokkaido Univ, Fac Agr, Dept Appl Biosci, Kita Ku, Sapporo, Hokkaido 0608589, JapanHokkaido Univ, Fac Agr, Dept Appl Biosci, Kita Ku, Sapporo, Hokkaido 0608589, Japan
Fukushi, Y
Tahara, S
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机构:Hokkaido Univ, Fac Agr, Dept Appl Biosci, Kita Ku, Sapporo, Hokkaido 0608589, Japan
机构:Hokkaido Univ, Fac Agr, Dept Appl Biosci, Kita Ku, Sapporo, Hokkaido 0608589, Japan
Fukui, H
Fukushi, Y
论文数: 0引用数: 0
h-index: 0
机构:
Hokkaido Univ, Fac Agr, Dept Appl Biosci, Kita Ku, Sapporo, Hokkaido 0608589, JapanHokkaido Univ, Fac Agr, Dept Appl Biosci, Kita Ku, Sapporo, Hokkaido 0608589, Japan
Fukushi, Y
Tahara, S
论文数: 0引用数: 0
h-index: 0
机构:Hokkaido Univ, Fac Agr, Dept Appl Biosci, Kita Ku, Sapporo, Hokkaido 0608589, Japan