Enantiomeric recognition of amino acids using a chiral spiropyran derivative | Zendy

Tsubaki Kazunori | Zendy; Mukoyoshi Koichiro | Zendy; Morikawa Hiroshi | Zendy; Kinoshita Takayoshi | Zendy; Fuji Kaoru | Zendy

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Enantiomeric recognition of amino acids using a chiral spiropyran derivative

Author(s) -

Tsubaki Kazunori,

Mukoyoshi Koichiro,

Morikawa Hiroshi,

Kinoshita Takayoshi,

Fuji Kaoru

Publication year - 2002

Publication title -

chirality

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.43

H-Index - 77

eISSN - 1520-636X

pISSN - 0899-0042

DOI - 10.1002/chir.10111

Subject(s) - spiropyran , chemistry , merocyanine , enantiomer , amino acid , moiety , derivative (finance) , stereochemistry , optically active , chirality (physics) , ionone , organic chemistry , photochromism , chiral symmetry breaking , biochemistry , physics , quantum mechanics , nambu–jona lasinio model , financial economics , economics , quark

An optically active spiropyran 1 with a binaphthol moiety as a chiral source was synthesized. The colored merocyanine form of ( R )‐ 1 obtained by the UV irradiation remained in the presence of D ‐amino acids longer than with L ‐amino acids. Chirality 14:713–715, 2002. © 2002 Wiley‐Liss, Inc.

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