Tetrahedron Asymmetry p. 785 - 788 (1991)
Update date:2022-08-05
Topics:
Giordano, Claudio
Restelli, Angelo
For the first time it is reported that 1,5-benzothiazepines (1a-e) (Figure 1) behave as effective chiral solvating agents (CSA) for NMR enantiomeric excess (ee) determination of different classes of compounds such as α-arylalkanoic acids, α-hydroxy acids,
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Doi:10.1016/j.poly.2013.02.003
(2013)Doi:10.1016/0040-4020(89)80044-4
(1989)Doi:10.1021/jo3012682
(2012)Doi:10.1016/j.tetlet.2008.03.092
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(1991)Doi:10.1039/c7ob00555e
(2017)
