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- W2109574023 endingPage "241" @default.
- W2109574023 startingPage "229" @default.
- W2109574023 abstract "Abstract Biomimetic studies of pyridoxal and pyridoxamine models are of both fundamental and practical interest. This review examines (i) deracemization of α‐amino acids with a chiral pyridoxal model, (ii) sensing of chirality of small molecules including α‐, β‐, and γ‐amino acids, peptides, amino alcohols and diamines with an achiral pyridoxal model and (iii) stereospecific synthesis of chiral diamines with a chiral pyridoxamine model. A binol‐based aldehyde is useful as a chiral pyridoxal model to deracemize a variety of α‐amino acids to make D ‐amino acids. 2,2′‐Dihydroxybenzophenone is useful as an achiral pyridoxal model for sensing the chirality of the above‐mentioned small molecules in a unified way. Bis(2‐hydroxyphenyl)‐ethylenediamine ( hpen ) is useful as a chiral pyridoxamine model for making chiral diamines. Weak forces (H‐bonding, steric and electronic effects) involved in transamination reactions with pyridoxamine for the synthesis of amino acids are compared with those for the diaza‐Cope rearrangement reaction with hpen for the synthesis of chiral diamines. Both experimental and computational methods are used to analyze the biomimetic systems." @default.
- W2109574023 created "2016-06-24" @default.
- W2109574023 creator A5008383067 @default.
- W2109574023 creator A5041629555 @default.
- W2109574023 creator A5077185233 @default.
- W2109574023 creator A5085447652 @default.
- W2109574023 date "2011-11-17" @default.
- W2109574023 modified "2023-10-18" @default.
- W2109574023 title "Mimicking Nature to Make Unnatural Amino Acids and Chiral Diamines" @default.
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