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Stereoselective hydroxylation by CYP2C19 and oxidation by ADH4 in the in vitro metabolism of tivantinib

Xenobiotica, 2016-11, Vol.46 (11), p.967-976

2016

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Syntheses of glucose derivatives of E5564-related compounds and their LPS-antagonistic activities

Carbohydrate research, 2006-05, Vol.341 (7), p.811-822

2006

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Synthesis of lipid A analogues containing glucose instead of glucosamine and their LPS-antagonistic activities

Tetrahedron, 2005-05, Vol.61 (21), p.5101-5122

2005

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From Penicillin to Penem and Carbapenem. VIII. Introduction of an Allyl Group at the C-4 Position of the Azetidinone Molecule, and the Synthesis of Dethiathienamycin

Bulletin of the Chemical Society of Japan, 1986-05, Vol.59 (5), p.1363-1369

1986

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Versatile Synthesis of an Intermediate for the 1b-Methylcarbapenem Synthesis

Heterocycles, 1994, Vol.38 (2), p.277

1994

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From Penicillin to Penem and Carbapenem. IX. C1-Unit Introduction and the Carbapenam Synthesis from the Penicillin Molecule

Bulletin of the Chemical Society of Japan, 1986-06, Vol.59 (6), p.1887-1896

1986

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Lipid A-Type Pyrancarboxylic Acid Derivatives, their Synthesis and their Biological Activities

Tetrahedron, 2000-09, Vol.56 (39), p.7691-7703

2000

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From penicillin to penem and carbapenem. VI1

Tetrahedron letters, 1985-01, Vol.26 (1), p.89-92

1985

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From penicillin to penem and carbapenem. II synthesis of 3,4-disubstituted azetidinone derivatives from 6,6-bis(phenylselenyl)penicillanate

Tetrahedron letters, 1982, Vol.23 (39), p.4021-4024

1982

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From Penicillin to Penem and Carbapenem. VII. : Synthesis and Antibacterial Activity of Penem Derivatives

Chemical and Pharmaceutical Bulletin, 1986/03/25, Vol.34(3), pp.999-1014

1986

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From penicillin to penem and carbapenem. IV Synthesis of 2-oxocarbapenam derivative

Tetrahedron letters, 1983, Vol.24 (31), p.3251-3254

1983

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Synthesis and biological activities of lipid A-type pyrancarboxylic acid derivatives

Carbohydrate research, 2000-03, Vol.324 (4), p.225-230

2000

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From Penicilin to Penem and Carbapenem. 1. Racemization of 6,6-Dibromo Secopenicillin, and Synthesis of 2-Oxo Penam Derivative

Heterocycles, 1982, Vol.17 (1), p.201

1982

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Synthesis of Δ1-carbapenem derivative by aldol condensation method

Tetrahedron letters, 1981-01, Vol.22 (11), p.1021-1024

1981

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A novel synthesis of 7-methoxycephalosporins and 6-methoxypenicillins

Tetrahedron letters, 1976-01, Vol.17 (16), p.1307-1310

1976

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Synthesis of Oxapenam Derivatives by Silver Induced Cyclization

Chemical and Pharmaceutical Bulletin, 1978/06/25, Vol.26(6), pp.1761-1767

1978

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7alpha-methoxylation of cephalosporins

Chemical & pharmaceutical bulletin, 1977-01, Vol.25 (2), p.369-370

1977

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Versatile synthesis of an intermediate for the 1β-methylcarbapenem synthesis

Heterocycles, 1994-02, Vol.38 (2), p.277-280

1994

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From penicillin to penem and carbapenem. III C1-unit introduction at C-4 position of azetidinone

Tetrahedron letters, 1982-01, Vol.23 (39), p.4025-4026

1982

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From penicillin to penem and carbapenem. V Synthesis ofcarbapenam skeleton by (3 + 2) cyclization

Tetrahedron letters, 1984, Vol.25 (11), p.1151-1154

1984

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From penicillin to penem and carbapenem. VI 1) : Synthesis of dethiathienamycin

Tetrahedron letters, 1985, Vol.26 (1), p.89-92

1985

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From penicillin to penem and carbapenem. VI: Synthesis of dethiathienamycin

Tetrahedron letters, 1985, Vol.26 (1), p.89-92

1985

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From penicillin to penem and carbapenem. III C 1-unit introduction at C-4 position of azetidinone

Tetrahedron letters, 1982, Vol.23 (39), p.4025-4026

1982

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A convenient synthesis of the β-lactam ring by 3 + 1 cyclization

Tetrahedron letters, 1979, Vol.20 (22), p.2031-2034

1979

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From Penicillin to Penem and Carbapenem. VII

Chemical & pharmaceutical bulletin, 1986-03, Vol.34 (3), p.999

1986

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Stereoselective hydroxylation by CYP2C19 and oxidation by ADH4 in the in vitro metabolism of tivantinib

Syntheses of glucose derivatives of E5564-related compounds and their LPS-antagonistic activities

Synthesis of lipid A analogues containing glucose instead of glucosamine and their LPS-antagonistic activities

From Penicillin to Penem and Carbapenem. VIII. Introduction of an Allyl Group at the C-4 Position of the Azetidinone Molecule, and the Synthesis of Dethiathienamycin

Versatile Synthesis of an Intermediate for the 1b-Methylcarbapenem Synthesis

From Penicillin to Penem and Carbapenem. IX. C1-Unit Introduction and the Carbapenam Synthesis from the Penicillin Molecule

Lipid A-Type Pyrancarboxylic Acid Derivatives, their Synthesis and their Biological Activities

From penicillin to penem and carbapenem. VI1

From penicillin to penem and carbapenem. II synthesis of 3,4-disubstituted azetidinone derivatives from 6,6-bis(phenylselenyl)penicillanate

From Penicillin to Penem and Carbapenem. VII. : Synthesis and Antibacterial Activity of Penem Derivatives

From penicillin to penem and carbapenem. IV Synthesis of 2-oxocarbapenam derivative

Synthesis and biological activities of lipid A-type pyrancarboxylic acid derivatives

From Penicilin to Penem and Carbapenem. 1. Racemization of 6,6-Dibromo Secopenicillin, and Synthesis of 2-Oxo Penam Derivative

Synthesis of Δ1-carbapenem derivative by aldol condensation method

A novel synthesis of 7-methoxycephalosporins and 6-methoxypenicillins

Synthesis of Oxapenam Derivatives by Silver Induced Cyclization

7alpha-methoxylation of cephalosporins

Versatile synthesis of an intermediate for the 1β-methylcarbapenem synthesis

From penicillin to penem and carbapenem. III C1-unit introduction at C-4 position of azetidinone

From penicillin to penem and carbapenem. V Synthesis ofcarbapenam skeleton by (3 + 2) cyclization

From penicillin to penem and carbapenem. VI 1) : Synthesis of dethiathienamycin

From penicillin to penem and carbapenem. VI: Synthesis of dethiathienamycin

From penicillin to penem and carbapenem. III C 1-unit introduction at C-4 position of azetidinone

A convenient synthesis of the β-lactam ring by 3 + 1 cyclization

From Penicillin to Penem and Carbapenem. VII

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