Stereospecific transformation of a chiral pyrimidyl alkanol into L-valine

Kenso Soai, Shigehisa Tanji, Yasutaka Kodaka, Takanori Shibata

研究成果: Article

5 引用 (Scopus)

抄録

A chiral pyrimidyl alkanol with high enantiomeric excess is transformed into L-valine with high e.e. by a notable oxidative cleavage of pyrimidine ring using ruthenium oxide as a key step. This process would correlate natural α-amino acids with a chiral pyrimidyl alkanol, which is reported to possess an asymmetric autocatalytic activity with amplification of e.e.

元の言語English
ページ(範囲)241-243
ページ数3
ジャーナルEnantiomer
3
発行部数3
出版物ステータスPublished - 1998
外部発表Yes

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Ruthenium
Valine
Oxides
Amplification
Amino Acids
pyrimidine

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Biochemistry
  • Chemistry(all)
  • Organic Chemistry

これを引用

Stereospecific transformation of a chiral pyrimidyl alkanol into L-valine. / Soai, Kenso; Tanji, Shigehisa; Kodaka, Yasutaka; Shibata, Takanori.

:: Enantiomer, 巻 3, 番号 3, 1998, p. 241-243.

研究成果: Article

Soai, K, Tanji, S, Kodaka, Y & Shibata, T 1998, 'Stereospecific transformation of a chiral pyrimidyl alkanol into L-valine', Enantiomer, 巻. 3, 番号 3, pp. 241-243.
Soai, Kenso ; Tanji, Shigehisa ; Kodaka, Yasutaka ; Shibata, Takanori. / Stereospecific transformation of a chiral pyrimidyl alkanol into L-valine. :: Enantiomer. 1998 ; 巻 3, 番号 3. pp. 241-243.
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