Lewis Base-Catalyzed Enantioselective Conjugate Reduction of ß,ß-Disubstituted &#945;,ß-Unsaturated Ketones with Trichlorosilane: <i>E</i>/<i>Z</i>-Isomerization, Regioselectivity, and Synthetic Applications.

Sugiura, Masaharu; Ashikari, Yasuhiko; Takahashi, Yuka; Yamaguchi, Koki; Kotani, Shunsuke; Nakajima, Makoto

Lewis Base-Catalyzed Enantioselective Conjugate Reduction of ß,ß-Disubstituted α,ß-Unsaturated Ketones with Trichlorosilane: E/Z-Isomerization, Regioselectivity, and Synthetic Applications.

Sugiura, Masaharu; Ashikari, Yasuhiko; Takahashi, Yuka; Yamaguchi, Koki; Kotani, Shunsuke; Nakajima, Makoto.

Afiliación

Sugiura M; Faculty of Pharmaceutical Sciences , Sojo University , 4-22-1 Ikeda , Nishi-ku, Kumamoto 860-0082 , Japan.
Ashikari Y; Graduate School of Pharmaceutical Sciences , Kumamoto University , 5-1 Oe-honmachi , Chuo-ku, Kumamoto 862-0973 , Japan.
Takahashi Y; Graduate School of Pharmaceutical Sciences , Kumamoto University , 5-1 Oe-honmachi , Chuo-ku, Kumamoto 862-0973 , Japan.
Yamaguchi K; Faculty of Pharmaceutical Sciences , Sojo University , 4-22-1 Ikeda , Nishi-ku, Kumamoto 860-0082 , Japan.
Kotani S; Graduate School of Pharmaceutical Sciences , Kumamoto University , 5-1 Oe-honmachi , Chuo-ku, Kumamoto 862-0973 , Japan.
Nakajima M; Graduate School of Pharmaceutical Sciences , Kumamoto University , 5-1 Oe-honmachi , Chuo-ku, Kumamoto 862-0973 , Japan.

J Org Chem ; 84(18): 11458-11473, 2019 09 20.

Article en En | MEDLINE | ID: mdl-31449412

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2019 Tipo del documento: Article País de afiliación: Japón

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