Asymmetric oxidation by new cyclic flavins with planar chirality (chiral flavinophanes)

Seiji Shinkai; Toshiro Yamaguchi; Akito Kawase; Akiyo Kitamura; Osamu Manabe

doi:10.1039/C39870001506

Asymmetric oxidation by new cyclic flavins with planar chirality (chiral flavinophanes)

Seiji Shinkai, Toshiro Yamaguchi, Akito Kawase, Akiyo Kitamura, Osamu Manabe

Research output: Contribution to journal › Article › peer-review

16 Citations (Scopus)

Abstract

Cyclic flavins with planar chirality (chiral flavinophanes) can oxidise thiols (ca. 43% enantiomeric excess) and NADH model compounds (ca. 60% enantiomeric excess) in an asymmetric manner.

Original language	English
Pages (from-to)	1506-1508
Number of pages	3
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	19
DOIs	https://doi.org/10.1039/C39870001506
Publication status	Published - 1987
Externally published	Yes

All Science Journal Classification (ASJC) codes

Molecular Medicine

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10.1039/C39870001506

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@article{31a27a1ea30b433395f67c371fbc490b,

title = "Asymmetric oxidation by new cyclic flavins with planar chirality (chiral flavinophanes)",

abstract = "Cyclic flavins with planar chirality (chiral flavinophanes) can oxidise thiols (ca. 43% enantiomeric excess) and NADH model compounds (ca. 60% enantiomeric excess) in an asymmetric manner.",

author = "Seiji Shinkai and Toshiro Yamaguchi and Akito Kawase and Akiyo Kitamura and Osamu Manabe",

year = "1987",

doi = "10.1039/C39870001506",

language = "English",

pages = "1506--1508",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "19",

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T1 - Asymmetric oxidation by new cyclic flavins with planar chirality (chiral flavinophanes)

AU - Shinkai, Seiji

AU - Yamaguchi, Toshiro

AU - Kawase, Akito

AU - Kitamura, Akiyo

AU - Manabe, Osamu

PY - 1987

Y1 - 1987

N2 - Cyclic flavins with planar chirality (chiral flavinophanes) can oxidise thiols (ca. 43% enantiomeric excess) and NADH model compounds (ca. 60% enantiomeric excess) in an asymmetric manner.

AB - Cyclic flavins with planar chirality (chiral flavinophanes) can oxidise thiols (ca. 43% enantiomeric excess) and NADH model compounds (ca. 60% enantiomeric excess) in an asymmetric manner.

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U2 - 10.1039/C39870001506

DO - 10.1039/C39870001506

M3 - Article

AN - SCOPUS:37049074316

SN - 1359-7345

SP - 1506

EP - 1508

JO - Chemical Communications

JF - Chemical Communications

IS - 19

ER -

Asymmetric oxidation by new cyclic flavins with planar chirality (chiral flavinophanes)

Abstract

All Science Journal Classification (ASJC) codes

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