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Muraminomicins, new lipo-nucleoside antibiotics from Streptosporangium sp. SANK 60501-structure elucidations of muraminomicins and supply of the core component for derivatization

Journal of antibiotics, 2019-12, Vol.72 (12), p.943-955

2019

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Muraminomicins, novel ester derivatives: in vitro and in vivo antistaphylococcal activity

Journal of antibiotics, 2019-12, Vol.72 (12), p.956-969

2019

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Design, Synthesis and Antifungal Activity of the Novel Water-Soluble Prodrug of Antifungal Triazole CS-758

Chemical and Pharmaceutical Bulletin, 2010/06/01, Vol.58(6), pp.794-804

2010

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Synthesis, cleavage, and antifungal activity of a number of novel, water-soluble ester prodrugs of antifungal triazole CS-758

Bioorganic & medicinal chemistry letters, 2009-07, Vol.19 (13), p.3559-3563

2009

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Synthesis and Antifungal Activities of R-102557 and Related Dioxane-Triazole Derivatives

Chemical and Pharmaceutical Bulletin, 2000/05/01, Vol.48(5), pp.694-707

2000

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Amide analogs of antifungal dioxane-triazole derivatives : Synthesis and in vitro activities

Bioorganic & medicinal chemistry letters, 2009-04, Vol.19 (7), p.2013-2017

2009

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Synthesis and in Vitro Antifungal Activities of Novel Triazole Antifungal Agent CS-758

Chemical and Pharmaceutical Bulletin, 2001, Vol.49(12), pp.1647-1650

2001

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Substituent effect of fluorine atoms in the 2,4-difluorophenyl group on antifungal activity of CS-758

Journal of fluorine chemistry, 2006-05, Vol.127 (4), p.643-650

2006

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Carbon analogs of antifungal dioxane-triazole derivatives: Synthesis and in vitro activities

Bioorganic & medicinal chemistry, 2008-12, Vol.18 (24), p.6538-6541

2008

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Synthesis of Racemic and Optically Active Cispentacin (FR109615) Using Intramolecular Nitrone-Olefin Cycloaddition

Chemical and Pharmaceutical Bulletin, 1993/06/15, Vol.41(6), pp.1012-1018

1993

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Enantiocontrolled Synthesis of the Antifungal β-Lactam (2R, 5S)-2-(Hydroxymethyl)clavam

Chemical and Pharmaceutical Bulletin, 1991/09/25, Vol.39(9), pp.2212-2215

1991

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Concise synthesis of optically active oxirane precursors for the preparation of triazole antifungals using the Friedel-Crafts reaction of ( S)-2-tosyloxypropionyl chloride

Tetrahedron letters, 1991-12, Vol.32 (51), p.7545-7548

1991

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Synthesis and evaluation of N-substituted 1,4-oxazepanyl sordaricins as selective fungal EF-2 inhibitors

Bioorganic & medicinal chemistry letters, 2002-07, Vol.12 (13), p.1705-1708

2002

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A novel approach to the stereoselective semi-synthesis of GM-237354 by employing a highly β-selective glycosylation

Tetrahedron letters, 2002-09, Vol.43 (38), p.6705-6708

2002

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Synthesis and evaluation of novel pyrrolidinyl sordaricin derivatives as antifungal agents

Bioorganic & medicinal chemistry letters, 2002-10, Vol.12 (19), p.2733-2736

2002

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Structural Study of Triazole Antifungals. II. Crystal and Molecular Structures of the Two Diastereoisomers (4R,5R)- and (4S,5R)-5-(2,4-Difluorophenyl)-4-methyl-5-[(1H-1,2,4-triazol-1-yl)methyl]-3-[4-(trifluoromethyl)benzoyl]oxazolidine

Bulletin of the Chemical Society of Japan, 1991-10, Vol.64 (10), p.2877-2881

1991

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Triazole Antifungals. II. : Synthesis and Antifungal Activities of 3-Acyl-4-methyloxazolidine Derivatives

Chemical and Pharmaceutical Bulletin, 1990/09/25, Vol.38(9), pp.2476-2486

1990

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Triazole Antifungals. IV. Synthesis and Antifungal Activities of 3-Acylamino-2-aryl-2-butanol Derivatives

Chemical and Pharmaceutical Bulletin, 1991/10/25, Vol.39(10), pp.2581-2589

1991

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Synthesis of Skeleton of Antitumor Quassinoid

Bulletin of the Chemical Society of Japan, 1988-10, Vol.61 (10), p.3587-3605

1988

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Synthesis of Sordaricin Analogues as Potent Antifungal Agents against Candida albicans

Bioorganic & medicinal chemistry letters, 2002-03, Vol.12 (5), p.803-806

2002

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Crystal Structure and Absolute Configuration of (2R, 3R)-(-)-2-(2, 4-dichlorophenyl)-3-azido-1-(1H-1, 2, 4-triazol-1-yl)-2-butanol

Analytical Sciences, 1990/10/10, Vol.6(5), pp.789-790

1990

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Synthesis and Antifungal Activities of Some Thiolane-Triazole Derivatives

Chemical and Pharmaceutical Bulletin, 1990/05/25, Vol.38(5), pp.1258-1265

1990

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β-Lactam Antifungals. II. Enantiocontrolled Synthesis of (2R, 5S)-2-Hydroxymethyl-1-carbapenam, the Carba-Analog of a Clavam Antifungal

Chemical and Pharmaceutical Bulletin, 1991/11/25, Vol.39(11), pp.2813-2818

1991

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Triazole Antifungals. III. Stereocontrolled Synthesis of an Optically Active Triazolylmethyloxirane Precursor to Antifungal Oxazolidine Derivatives

Chemical and Pharmaceutical Bulletin, 1991/09/25, Vol.39(9), pp.2241-2246

1991

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Payne rearrangement route to the optically active oxirane precursor for the preparation of trizole antifungals

Chemical & pharmaceutical bulletin, 1992, Vol.40 (2), p.562-564

1992

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Muraminomicins, new lipo-nucleoside antibiotics from Streptosporangium sp. SANK 60501-structure elucidations of muraminomicins and supply of the core component for derivatization

Muraminomicins, novel ester derivatives: in vitro and in vivo antistaphylococcal activity

Design, Synthesis and Antifungal Activity of the Novel Water-Soluble Prodrug of Antifungal Triazole CS-758

Synthesis, cleavage, and antifungal activity of a number of novel, water-soluble ester prodrugs of antifungal triazole CS-758

Synthesis and Antifungal Activities of R-102557 and Related Dioxane-Triazole Derivatives

Amide analogs of antifungal dioxane-triazole derivatives : Synthesis and in vitro activities

Synthesis and in Vitro Antifungal Activities of Novel Triazole Antifungal Agent CS-758

Substituent effect of fluorine atoms in the 2,4-difluorophenyl group on antifungal activity of CS-758

Carbon analogs of antifungal dioxane-triazole derivatives: Synthesis and in vitro activities

Synthesis of Racemic and Optically Active Cispentacin (FR109615) Using Intramolecular Nitrone-Olefin Cycloaddition

Enantiocontrolled Synthesis of the Antifungal β-Lactam (2R, 5S)-2-(Hydroxymethyl)clavam

Concise synthesis of optically active oxirane precursors for the preparation of triazole antifungals using the Friedel-Crafts reaction of ( S)-2-tosyloxypropionyl chloride

Synthesis and evaluation of N-substituted 1,4-oxazepanyl sordaricins as selective fungal EF-2 inhibitors

A novel approach to the stereoselective semi-synthesis of GM-237354 by employing a highly β-selective glycosylation

Synthesis and evaluation of novel pyrrolidinyl sordaricin derivatives as antifungal agents

Structural Study of Triazole Antifungals. II. Crystal and Molecular Structures of the Two Diastereoisomers (4R,5R)- and (4S,5R)-5-(2,4-Difluorophenyl)-4-methyl-5-[(1H-1,2,4-triazol-1-yl)methyl]-3-[4-(trifluoromethyl)benzoyl]oxazolidine

Triazole Antifungals. II. : Synthesis and Antifungal Activities of 3-Acyl-4-methyloxazolidine Derivatives

Triazole Antifungals. IV. Synthesis and Antifungal Activities of 3-Acylamino-2-aryl-2-butanol Derivatives

Synthesis of Skeleton of Antitumor Quassinoid

Synthesis of Sordaricin Analogues as Potent Antifungal Agents against Candida albicans

Crystal Structure and Absolute Configuration of (2R, 3R)-(-)-2-(2, 4-dichlorophenyl)-3-azido-1-(1H-1, 2, 4-triazol-1-yl)-2-butanol

Synthesis and Antifungal Activities of Some Thiolane-Triazole Derivatives

β-Lactam Antifungals. II. Enantiocontrolled Synthesis of (2R, 5S)-2-Hydroxymethyl-1-carbapenam, the Carba-Analog of a Clavam Antifungal

Triazole Antifungals. III. Stereocontrolled Synthesis of an Optically Active Triazolylmethyloxirane Precursor to Antifungal Oxazolidine Derivatives

Payne rearrangement route to the optically active oxirane precursor for the preparation of trizole antifungals

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