Challenging the absence of observable hydrogens in the assignment of absolute configurations by NMR: application to chiral primary alcohols

Literature Information

Publication Date 2007-01-30
DOI 10.1039/B617184B
Impact Factor 6.222
Authors

Félix Freire, José Manuel Seco, Emilio Quiñoá, Ricardo Riguera


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Abstract

The absolute configuration of β-chiral primary alcohols devoid of observable hydrogens on one of the β-substituents at the asymmetric carbon (L1/L2) can be determined by comparison of the 1H NMR of their (R)- and (S)-9-AMA ester derivatives and analysis of the ΔδRS for the L substituent and the Cβ-H.

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