A catalytic enantioselective reaction using a C2-symmetric disulfonamide as a chiral ligand: Alkylation of aldehydes catalyzed by disulfonamide-Ti(O-i-Pr)4-Dialkyl zinc system

Ohno, Masaji.; Takahashi, Hideyo; Kobayashi, Susumu; Yoshioka, Masato; Kawakita, Takashi

doi:10.1016/0040-4020(92)80020-G

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A catalytic enantioselective reaction using a C2-symmetric disulfonamide as a chiral ligand: Alkylation of aldehydes catalyzed by disulfonamide-Ti(O-i-Pr)4-Dialkyl zinc system

Author(s): Hideyo Takahashi , Takashi Kawakita , Masaji Ohno , Masato Yoshioka , Susumu Kobayashi

Publication date Created: July 1992

Publication date (Print): July 1992

Journal: Tetrahedron

Publisher: Elsevier BV

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Resolution of racemic mixtures via lipase catalysis in organic solvents

Alexander M. Klibanov, Mark Scollar, Gerald Kirchner (1985)

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Asymmetric Diels-Alder reaction catalyzed by a chiral titanium reagent

Jun Sugimori, Masayuki Inoue, Tohru Yamada … (1989)

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Designed catalyst for enantioselective Diels-Alder addition from a C2-symmetric chiral bis(oxazoline)-iron(III) complex

E Corey, Hong Yue Zhang, Nobuyuki Imai (1991)

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Author and article information

Journal

Title: Tetrahedron

Abbreviated Title: Tetrahedron

Publisher: Elsevier BV

ISSN (Print): 00404020

Publication date Created: July 1992

Publication date (Print): July 1992

Volume: 48

Issue: 27

Pages: 5691-5700

Article

DOI: 10.1016/0040-4020(92)80020-G

SO-VID: 17a60814-ff96-4ce6-8a18-b37c64dc02b8

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A catalytic enantioselective reaction using a C2-symmetric disulfonamide as a chiral ligand: Alkylation of aldehydes catalyzed by disulfonamide-Ti(O-i-Pr)4-Dialkyl zinc system

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Genome Engineering using CRISPR

Most cited references 32

Resolution of racemic mixtures via lipase catalysis in organic solvents

Asymmetric Diels-Alder reaction catalyzed by a chiral titanium reagent

Designed catalyst for enantioselective Diels-Alder addition from a C2-symmetric chiral bis(oxazoline)-iron(III) complex

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