Conformational analysis of MαNP esters, powerful chiral resolution and 1H NMR anisotropy tools - aromatic geometry and solvent effects on Δδ values

Yusuke Kasai, Akinori Sugio, Satoshi Sekiguchi, Shunsuke Kuwahara, Takatoshi Matsumoto, Masataka Watanabe, Akio Ichikawa, Nobuyuki Harada

研究成果: Article

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The MαNP acid method is very powerful for the preparation of enantiopure alcohols by resolution and the simultaneous determination of their absolute configurations by the 1H NMR anisotropy effect, where the syn-syn conformation is taken as the preferred conformation of MαNP esters. However, the syn-syn conformation of MαNP esters looks unstable, because two electronegative oxygen atoms {CH3O and C=O} are close to each other. To solve the problem of why the MαNP esters take such a syn-syn conformation, the aromatic geometry and solvent effects on the 1H NMR anisotropy data were studied, leading to the following conclusions: i) the hydrogen-bonding-like interaction among the H-8′ of the naphthyl group, the ester carbonyl oxygen, and the methoxy oxygen supports a triangular intramolecular force to stabilize the syn-syn conformation; ii) triangular hydrogen bonding among a hydrogen atom of protic solvents, the ester carbonyl oxygen, and the methoxy oxygen also supports the syn-syn conformation. This hydrogen bonding, as the solvation effect implies, suggests that a similar hydrogen bonding between a MαNP ester and a hydroxy group of the silica gel surface would make a dominant contribution to the excellent Discrimination of diastereomeric MαNP esters observed in the HPLC on silica gel.

元の言語English
ページ(範囲)1811-1826
ページ数16
ジャーナルEuropean Journal of Organic Chemistry
発行部数11
DOI
出版物ステータスPublished - 2007 6 22

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry

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