Susumu Akutagawa
Takasago International Corporation
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Susumu Akutagawa.
Applied Catalysis A-general | 1995
Susumu Akutagawa
Abstract This article covers catalytic asymmetric syntheses effected by BINAP (R or S 2,2′-diphenylphosphino-1,1′-binaphthyl) ligand. The atropisomeric ligand is outstanding in its extremely high enantioselective recognition of hydrogen, when coordinated to rhodium or ruthenium metal. A unique chiral multiplication (asymmetric catalysis) derived from the isomerization of allylic amines to enamines by Rh-BINAP catalysis is reviewed from discovery to industrialization. The catalyst converted isoprenoid allylic amine to citronellal enamine in perfect selectivities (99% yield and 98% enantiomer excess) and activity (TON > 400 000) that promised the commercial manufacturing of enantiomerically pure terpene aldehydes. The industrial application of the highly sensitive and expensive Rh-BINAP catalyst for the production of 1500 t/y scale of chiral terpene compounds is introduced with some technical know how. A series of new ruthenium BINAP complexes was prepared and evaluated for asymmetric hydrogenation. Neutral Ru-BINAP dicarboxylato complexes catalyzed the hydrogenation of activated carbon-carbon double bonds enantioselectively. Prochiral unsaturated substrates including α-(acylamino)acrylic acids, allylic alcohols, α,β-unsaturated carboxylic acids and cyclic enamides were easily reduced to give saturated products in quantitative yields with 90–99% enantiomer excesses. Cationic Ru-BINAP complexes catalyzed the hydrogenation of functionalized ketones enantioselectively. Prochiral ketones bearing hetero atom-containing functional groups at α,β or γ position were smoothly reduced affording corresponding alcohols in quantitative yields with high enantiomeric excesses. Industrial applications of these methodologies for pharmaceuticals and new materials are summarized.
Topics in Catalysis | 1997
Susumu Akutagawa
Enantioselective isomerizations of allylamines to enamines are summarized from idea to industry. The Rh–BINAP catalyst reveals high selectivities, 99% yield and 98% enantiomer excess and high activity, TON > 400,000. Its industrial use for the production of a 1,500 t/y scale of (–)-menthol is introduced emphasizing technical development.
Archive | 1988
Noboru Sayo; Takao Saito; Hidenori Kumobayashi; Susumu Akutagawa; Ryoji Noyori; Hidemasa Takaya
Archive | 1985
Sadao Yoshikawa; Masahiko Saburi; Takao Ikariya; Youichi Ishii; Susumu Akutagawa
Archive | 1987
Hidemasa Takaya; Tetsuo Ohta; Ryoji Noyori; Noboru Sayo; Hidenori Kumobayashi; Susumu Akutagawa
Archive | 2011
Hidemasa Takaya; Tetsuo Ohta; Ryoji Noyori; Noboru Sayo; Hidenori Kumobayashi; Susumu Akutagawa
Archive | 1989
Shigeru Mitsuhashi; Hitoshi Kondo; Tetsuharu Okazaki; Shinji Endoh; Hiroko Kudo; Akio Yamaguchi; Haruki Tsuruta; Susumu Akutagawa
Archive | 1991
Takanao Taketomi; Susumu Akutagawa; Hidenori Kumobayashi; Hidemasa Takaya; Kazushi Mashima
ChemInform | 2005
Susumu Akutagawa; Kazuhide Tani
Archive | 1993
Akio Yamaguchi; Yoji Hori; Susumu Akutagawa