H. Ohmizu

发表

Electroorganic chemistry. 62. Reaction of iminium ion with nucleophile: a versatile synthesis of tetrahydroquinolines and julolidines

T. Shono, Y. Matsumura, Kenji Inoue, 1982 .

Quantitative structure-activity analyses of novel hydroxyphenylurea derivatives as antioxidants.

T. Fujita, H. Kubota, H. Ohmizu, 1998, Bioorganic & medicinal chemistry.

Antioxidative property of T-0970, a new ureidophenol derivative

H. Kubota, H. Ohmizu, T. Suzuki, 2000, Free radical research.

Electroorganic chemistry. 62. Reaction of iminium ion with nucleophile: a versatile synthesis of tetrahydroquinolines and julolidines

T. Shono, Y. Matsumura, Kenji Inoue, 1982 .

Design, synthesis, and evaluation of orally active inhibitors of plasminogen activator inhibitor-1 (PAI-1) production.

H. Ohmizu, H. Miyazaki, T. Ogiku, 2008, Bioorganic & medicinal chemistry letters.

Synthesis and evaluation of 1,4-diphenylbutadiene derivatives as inhibitors of plasminogen activator inhibitor-1 (PAI-1) production.

H. Ohmizu, H. Miyazaki, T. Ogiku, 2010, Bioorganic & medicinal chemistry.

Evaluation of pyrrolin-2-one derivatives synthesized by a new practical method as inhibitors of plasminogen activator inhibitor-1 (PAI-1).

H. Ohmizu, H. Miyazaki, T. Miyake, 2010, Bioorganic & medicinal chemistry letters.

Facile Stereoselective Synthesis of (E)- and (Z)-α-Substituted Cinnamates: Stereospecific Dehydration Reaction with 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) and Copper(II) Chloride.

H. Ohmizu, T. Ogiku, H. Sai, 2008 .

A NOVEL SYNTHESIS OF TERMINAL OLEFINS BY ANODIC OXIDATION OF CARBOXYLIC ACIDS HAVING A TRIMETHYLSILYL GROUP ON THE β-POSITION

T. Shono, H. Ohmizu, N. Kise, 1980 .

Novel selective synthesis of α-chloromethyl, α,α-dichloromethyl, and α,α,α-trichloromethyl ketones from aldehyde utilizing electroreduction as key reactions

T. Shono, H. Ohmizu, N. Kise, 1982 .

Novel synthesis of carbohydrates using electroreduction as key reactions

T. Shono, H. Ohmizu, N. Kise, 1982 .

A novel chain reaction induced by cathodic reduction. Addition of trichloromethyl anion to aldehydes or vimyl acetate

T. Shono, H. Ohmizu, N. Kise, 1981 .

Electroorganic chemistry. 31. Reductive cyclization of nonconjugated olefinic ketones to cyclic tertiary alcohols

T. Shono, H. Ohmizu, I. Nishiguchi, 1978 .

A facile synthesis of the key intermediate for penems, carbapenems, and related β-lactam antibiotics

H. Ohmizu, M. Seki, T. Miyake, 1996 .

Highly stereoselective and practical synthesis of a key intermediate for 1-β-methylcarbapenems

H. Ohmizu, M. Seki, T. Yamanaka, 1996 .

A novel synthesis of a key intermediate for penems and carbapenems utilizing lipase-catalyzed kinetic resolution

H. Ohmizu, M. Seki, T. Miyake, 1996 .

New Synthesis of 2,6-Diaryl-4-oxo-3,7-dioxabicyclo[3.3.0]octanes: Synthesis of (±)-Styraxin

H. Ohmizu, S. Yoshida, T. Ogiku, 1997 .

First Stereocontrolled Syntheses of Unsymmetrically Substituted Bislactone Lignans: Stereocontrolled Syntheses of Four Possible Isomers of Methyl 4,8-Dioxoxanthoxylol

H. Ohmizu, S. Yoshida, T. Ogiku, 1997 .

Quinazolin-2-ones Having a Spirohydantoin Ring.I. : Synthesis of Spiro[1, 2, 3, 4-tetrahydroquinazoline-4, 4'-imidazolidine]-2, 2', 5'-trione by Reaction of 1-Carbamoylisatin with Uera or Guanidine

H. Ohmizu, Yoshihisa Yamada, K. Ozaki, 1990 .

EFFICIENT SYNTHESES OF 1-ARYLNAPHTHALENE LIGNAN LACTONES AND RELATED COMPOUNDS FROM CYANOHYDRINS

H. Ohmizu, S. Yoshida, T. Ogiku, 1995 .

Stereoselective Syntheses of Lignans Utilizing Cyanohydrins

H. Ohmizu, T. Iwasaki, 1995 .

A New Synthesis of Arylnaphthalene Lignan Lactones

H. Ohmizu, S. Yoshida, T. Ogiku, 1992 .

A new two-step synthesis of 1-arylnaphthalene lignans from cyanohydrins

H. Ohmizu, T. Ogiku, M. Takahashi, 1990 .

Stereoselective Syntheses of (E)-α,β-Dehydroamino Acids and (E)-α,β-Dehydropeptides by Stereospecific Dehydration with 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC)

H. Ohmizu, T. Ogiku, H. Sai, 2003 .

A Novel Synthesis of a Key Intermediate for Penems and Carbapenems Utilizing Lipase-Catalyzed Kinetic Resolution.

H. Ohmizu, M. Seki, T. Miyake, 1996 .

Highly Stereoselective and Practical Synthesis of a Key Intermediate for 1-β-Methylcarbapenems.

H. Ohmizu, M. Seki, T. Yamanaka, 1996 .

A Facile Synthesis of the Key Intermediate for Penems, Carbapenems, and Related β-Lactam Antibiotics.

H. Ohmizu, M. Seki, T. Miyake, 1996 .

Electroreductive crossed hydrocoupling of aromatic ketones with enol acetates

T. Shono, H. Ohmizu, S. Kawakami, 1979 .

A new synthesis of 2,2′-disubstituted unsymmetrical biphenyls based on the intramolecular Ullmann coupling reaction utilising salicyl alcohol as a template

H. Ohmizu, K. Kondo, T. Ogiku, 1993 .

Facile stereoselective synthesis of (E)- and (Z)-α-substituted cinnamates: stereospecific dehydration reaction with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) and copper(II) chloride

H. Ohmizu, T. Ogiku, H. Sai, 2007 .

Novel Synthesis of Highly Functionalized Unsymmetrical Biphenyls

H. Ohmizu, K. Kondo, S. Yoshida, 1994 .

Asymmetric syntheses of lignans utilizing novel diastereoselective Michael addition of cyanohydrin: Syntheses of (+)-fargesin and (−)-picropodophyllone

H. Ohmizu, Y. Moritani, T. Miyake, 1997 .

Stereoselective Syntheses of Cis- and Trans-Isomers of alpha-Hydroxy-alpha,beta-dibenzyl-gamma-butyrolactone Lignans: New Syntheses of (+/-)-Trachelogenin and (+/-)-Guayadequiol.

T. Ukita, H. Ohmizu, T. Miyagishima, 1996, The Journal of organic chemistry.

Facile stereoselective syntheses of (E)- and (Z) -α-substituted cinnamates by stereoselective dehydration reaction with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC)

H. Ohmizu, H. Sai, 1999 .

A new synthesis of unsymmetrical diphenic acid derivatives: template-directed intramolecular Ullmann coupling reaction

H. Ohmizu, K. Kondo, T. Ogiku, 1991 .

Electroreductive acylation of benzyl chloride and related compounds with acid chlorides.

T. Shono, H. Ohmizu, I. Nishiguchi, 1977 .

Electroreductive hydrocoupling of activated olefins with ketones or aldehydes in the presence of trimethylchlorosilane

H. Sugiyama, T. Shono, H. Ohmizu, 1980 .

Electroorganic chemistry. 30. A novel acylation of some activated olefins by electroreductive method

T. Shono, H. Ohmizu, I. Nishiguchi, 1977 .

A new stereocontrolled synthesis of diequatorial furofuran lignans having two different aryl groups: A synthesis of methyl piperitol

H. Ohmizu, S. Yoshida, T. Ogiku, 1992 .

AN EFFICIENT SYNTHESIS OF HETEROCYCLIC ANALOGS OF 1-ARYLNAPHTHALENE LIGANDS

H. Ohmizu, T. Nishitani, K. Kondo, 1994 .

Synthesis of verrucarin A

W. C. Still, H. Ohmizu, 1981 .

Stereoselective Syntheses of cis‐ and trans‐Isomers of α‐Hydroxy‐ α,β‐dibenzyl‐γ‐butyrolactone Lignans: New Syntheses of (.+‐.)‐Trachelogenin and (.+‐.)‐Guayadequiol.

T. Ukita, H. Ohmizu, T. Miyagishima, 2010 .

A new stereocontrolled synthesis of axial-equatorial furofuran lignans having two different aryl groups: A synthesis of Fargesin

H. Ohmizu, S. Yoshida, T. Ogiku, 1992 .

Stereocontrolled Syntheses of Diequatorial and Axial-Equatorial Furofuran Lignans

H. Ohmizu, S. Yoshida, T. Ogiku, 1995 .

Novel hydroxyphenylurea dual inhibitor against acyl-CoA: cholesterol acyltransferase (ACAT) and low density lipoprotein (LDL) oxidation as antiatherosclerotic agent.

H. Kubota, H. Ohmizu, K. Nakao, 2001, Bioorganic & medicinal chemistry.

Synthesis and evaluation of pyrrolin-2-one compounds, a series of plasminogen activator inhibitor-1 inhibitors.

H. Ohmizu, Y. Moritani, H. Miyazaki, 2009, Chemical & pharmaceutical bulletin.

The first stereocontrolled synthesis of axial-equatorial bislactone furofuran lignans having two different aryl groups: A synthesis of methyl 4, 8-dioxoxanthoxylol

H. Ohmizu, S. Yoshida, T. Ogiku, 1995 .

Practical Synthetic Method of (2Z,3E)-1,4-Diphenylbutadiene T-2639, an Inhibitor of Plasminogen Activator Inhibitor-1 (PAI-1) Production

H. Ohmizu, H. Miyazaki, T. Ogiku, 2009 .

An efficient synthesis of highly functionalized unsymmetrical biphenyls having substituents on the ortho positions

H. Ohmizu, Y. Moritani, K. Kondo, 1992 .

Synthesis of 1,4-diphenylbutadiene derivatives: novel inducer of tissue-type plasminogen activator (t-PA) in cultured bovine endothelial cells.

H. Ohmizu, T. Ogiku, H. Sai, 2006, Chemical & pharmaceutical bulletin.

Major proteins released by a protein-producing bacterium, Bacillus brevis 47, are derived from cell wall protein.

H. Ohmizu, K. Yagi, N. Tsukagoshi, 1983, Journal of biochemistry.

Simple Synthesis of trans-.ALPHA.,.BETA.-Dibenzyl-.GAMMA.-butyrolactone Lignans by Diastereoselective Reduction of .ALPHA.-Benzylidene-.BETA.-benzyl-.GAMMA.-butyrolactones Using NaBH4-NiCl2.

H. Ohmizu, T. Miyagishima, Y. Moritani, 1996 .

Simple Synthesis of trans‐α,β‐Dibenzyl‐γ‐ butyrolactone Lignans by Diastereoselective Reduction of α‐ Benzylidene‐β‐benzyl‐γ‐butyrolactones Using NaBH4‐NiCl2.

H. Ohmizu, T. Miyagishima, Y. Moritani, 1996 .

A Facile Synthesis of Highly Functionalized Unsymmetrical Heterobiaryls Utilizing the Intramolecular Ullmann Coupling Reaction Directed by Salicyl Alcohol as a Template

H. Ohmizu, K. Kondo, T. Ogiku, 1992 .

A highly stereoselective synthesis of 3-hydroxy-1-aryltetralin lignans based on the stereoselective hydroxylation of α,β-dibenzyl-γ-butyro-lactones: the first synthesis of (±)-cycloolivil

T. Ukita, H. Ohmizu, Y. Moritani, 1996 .

A Highly Stereoselective Synthesis of 3-Hydroxy-1-aryltetralin Lignans based on the Stereoselective Hydroxylation of α,β-Dibenzyl-. gamma.-butyrolactones: The First Synthesis of (.+-.)-Cycloolivil.

T. Ukita, H. Ohmizu, Y. Moritani, 1997 .

Syntheses of Aryltetralin Lignans: Concise Syntheses of (±)-Isopodophyllotoxone, (±)-Picropodophyllone and Their Related Compounds

H. Ohmizu, S. Yoshida, T. Ogiku, 1992 .

A novel asymmetric synthesis of axial-equatorial furofuran lignans: A synthesis of (+)-fargesin

H. Ohmizu, Y. Moritani, T. Miyake, 1995 .

The first synthesis of (±)-cycloolivil: a highly stereoselective synthesis of 3-hydroxy-1-aryltetralin lignans based on the stereoselective hydroxylation of α,β-dibenzyl-γ-butyrolactones

T. Ukita, H. Ohmizu, Y. Moritani, 1995 .

A Facile Synthesis of Highly Functionalized Unsymmetrical Heterobiaryls Utilizing the Intramolecular Ullmann Coupling Reaction Directed by Salicyl Alcohol as a Template.

H. Ohmizu, K. Kondo, T. Ogiku, 2010 .