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Kinetic resolution of 1,1'-binaphthyl-2,2'-diamine derivatives by chiral calcium phosphate-catalyzed acylation.
Uchikura, Tatsuhiro; Kanno, Yuki; Fukuda, Yukino; Sato, Mikoto; Akiyama, Takahiko.
Afiliação
  • Uchikura T; Department of Chemistry, Faculty of Science, Gakushuin University, 1-5-1, Mejiro, Toshima-ku, Tokyo, Japan. takahiko.akiyama@gakushuin.ac.jp.
  • Kanno Y; Department of Chemistry, Faculty of Science, Gakushuin University, 1-5-1, Mejiro, Toshima-ku, Tokyo, Japan. takahiko.akiyama@gakushuin.ac.jp.
  • Fukuda Y; Department of Chemistry, Faculty of Science, Gakushuin University, 1-5-1, Mejiro, Toshima-ku, Tokyo, Japan. takahiko.akiyama@gakushuin.ac.jp.
  • Sato M; Department of Chemistry, Faculty of Science, Gakushuin University, 1-5-1, Mejiro, Toshima-ku, Tokyo, Japan. takahiko.akiyama@gakushuin.ac.jp.
  • Akiyama T; Department of Chemistry, Faculty of Science, Gakushuin University, 1-5-1, Mejiro, Toshima-ku, Tokyo, Japan. takahiko.akiyama@gakushuin.ac.jp.
Org Biomol Chem ; 22(17): 3444-3447, 2024 May 01.
Article em En | MEDLINE | ID: mdl-38595221
ABSTRACT
1,1'-Binaphthyl-2,2'-diamine (BINAM) is a useful axially chiral compound. The kinetic resolution of BINAM is one of the most crucial methods for synthesizing chiral BINAM. We have developed a chiral calcium phosphate-catalyzed kinetic resolution of BINAM by utilizing an acylation reaction to produce a mono-amide. The kinetic resolution of BINAM derivatives was achieved by using isobutyric anhydride in the presence of chiral calcium phosphate and 4-morpholinopyridine with up to s = 127. 6,6'-Substituted BINAM derivatives were also applicable for this reaction. The resulting mono-acylated BINAM could be transformed into BINAM by hydrolysis under acidic conditions.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article