Switching enantiofacial selectivities using one chiral source: catalytic enantioselective synthesis of the key intermediate for (20S)-camptothecin family by (S)-selective cyanosilylation of ketones. | J Am Chem Soc;123(40): 9908-9, 2001 Oct 10. | MEDLINE

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Switching enantiofacial selectivities using one chiral source: catalytic enantioselective synthesis of the key intermediate for (20S)-camptothecin family by (S)-selective cyanosilylation of ketones.

Yabu, K; Masumoto, S; Yamasaki, S; Hamashima, Y; Kanai, M; Du, W; Curran, D P; Shibasaki, M.

Affiliation

Yabu K; Graduate School of Pharmaceutical Sciences, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

J Am Chem Soc ; 123(40): 9908-9, 2001 Oct 10.

Article in En | MEDLINE | ID: mdl-11583560

Subject(s)

Camptothecin/chemical synthesis; Cyanides/chemistry; Trimethylsilyl Compounds/chemistry; Glucose/chemistry; Stereoisomerism

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Collection: 01-internacional Database: MEDLINE Main subject: Trimethylsilyl Compounds / Camptothecin / Cyanides Language: En Journal: J Am Chem Soc Year: 2001 Document type: Article Affiliation country: Japan

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Collection: 01-internacional Database: MEDLINE Main subject: Trimethylsilyl Compounds / Camptothecin / Cyanides Language: En Journal: J Am Chem Soc Year: 2001 Document type: Article Affiliation country: Japan