cheminform abstract: asymmetric addition of nucleophiles to c-1 position of isoquinolines using...

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2002 isoquinoline derivatives isoquinoline derivatives R 0420 08 - 146 Asymmetric Addition of Nucleophiles to C-1 Position of Isoquino- lines Using (S)-Alanine Derivatives as Chiral Auxiliaries. The title reaction offers a general and highly stereoselective method to prepare 1-substituted tetrahydroisoquinolines which are of biological interest. Intro- duction of bromo groups on the substrate efficiently increases both chemical yield and stereoselectivity. — (ITOH, TAKASHI; NAGATA, KAZUHIRO; MIYAZAKI, MICHIKO; KAMEOKA, KEIKO; OHSAWA, AKIO; Tetrahedron 57 (2001) 42, 8827-8839; Sch. Pharm. Sci., Showa Univ., Shinagawa, Tokyo 142, Japan; EN) 1

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2002 isoquinoline derivatives

isoquinoline derivativesR 0420

08 - 146Asymmetric Addition of Nucleophiles to C-1 Position of Isoquino-lines Using (S)-Alanine Derivatives as Chiral Auxiliaries. — Thetitle reaction offers a general and highly stereoselective method to prepare1-substituted tetrahydroisoquinolines which are of biological interest. Intro-duction of bromo groups on the substrate efficiently increases both chemicalyield and stereoselectivity. — (ITOH, TAKASHI; NAGATA, KAZUHIRO;MIYAZAKI, MICHIKO; KAMEOKA, KEIKO; OHSAWA, AKIO; Tetrahedron57 (2001) 42, 8827-8839; Sch. Pharm. Sci., Showa Univ., Shinagawa, Tokyo142, Japan; EN)

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