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Intracerebroventricular administration of histamine H3 receptor antagonists decreases seizures in rat models of epilepsia

Methods and findings in experimental and clinical pharmacology, 2004-05, Vol.26 (4), p.263-270

2004

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Design and synthesis of an aminobenzo-15-crown-5-labeled estradiol tethered with disulfide linkage

Tetrahedron, 2004-12, Vol.60 (51), p.11911-11922

2004

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Nucleobase Participation in Ribozyme Catalysis

Journal of the American Chemical Society, 2005-04, Vol.127 (14), p.5026-5027

2005

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A Selective Human H 4 -Receptor Agonist: (−)-2-Cyano-1-methyl-3-{(2 R ,5 R )-5- [1 H -imidazol-4(5)-yl]tetrahydrofuran-2-yl}methylguanidine

Journal of medicinal chemistry, 2003-07, Vol.46 (14), p.3162-3165

2003

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Efficient and β-Stereoselective Synthesis of Pyrazole C-Nucleosides

Synthesis (Stuttgart), 2006-03, Vol.2006 (5), p.793-798

2006

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Synthesis of novel C4-linked imidazole ribonucleoside phosphoramidites for probing general acid and base catalysis in ribozyme

Tetrahedron, 2005-12, Vol.61 (50), p.11976-11985

2005

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Accurate molecular weight measurements of nucleoside phosphoramidites: a suitable matrix of mass spectrometry

Tetrahedron, 2005-05, Vol.61 (19), p.4689-4699

2005

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(13-Methyl-1,4,7,8,13,13b-hexahydro[1',2']oxazepino[2',3':1,2]pyrido[3,4-b]indol-1-yl)methanol and its Unusual Packing Style

Acta crystallographica. Section C, Crystal structure communications, 1995-01, Vol.51 (1), p.135-139

1995

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Efficient and beta-Stereoselective Synthesis of 4(5)-(beta-D-Ribofuranosyl)- and 4(5)-(2-Deoxyribofuranosyl)imidazoles(1)

Journal of organic chemistry, 1996-06, Vol.61 (13), p.4405-4411

1996

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Formation of Two 4-Imidazolylmethylphosphonium Salts and their Synthetic Studies Toward Histamine H 3 -Ligands

Synthesis (Stuttgart), 2003-12 (18), p.2844-2850

2003

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An efficient synthesis of magallanesine using [1,2]-Meisenheimer rearrangement and Heck cyclization

Tetrahedron, 1996-11, Vol.52 (46), p.14563-14576

1996

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Synthesis of imifuramine and its stereoisomers exhibiting histamine H 3-agonistic activity

Tetrahedron letters, 1999-03, Vol.40 (13), p.2561-2564

1999

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Synthesis of 4(5)-(a-D-Xylofuranosyl)imidazole Starting from L-Arabinose: Mitsunobu Cyclization via C4’-Oxyphosphonium Intermediate

Heterocycles, 2001-10, Vol.55 (10), p.1907

2001

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Cyano phosphate: an efficient intermediate for the chemoselective conversion of carbonyl compounds to nitriles

Journal of organic chemistry, 1991-03, Vol.56 (5), p.1827-1832

1991

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Stereoselective synthesis of the C-4 linked imidazole nucleosides using modified Mitsunobu reaction

Tetrahedron letters, 1995-05, Vol.36 (18), p.3165-3168

1995

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A synthesis of taxusin

Journal of the American Chemical Society, 1988-09, Vol.110 (19), p.6558-6560

1988

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Synthesis of an indole analog of magallanesine via the [1,2]-meisenheimer rearrangement

Journal of heterocyclic chemistry, 1996-11, Vol.33 (6), p.1909-1913

1996

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Studies on the [2, 3]-Meisenheimer Rearrangement of 2-Vinylazetidine N-Oxides

Chemical and Pharmaceutical Bulletin, 1998/05/15, Vol.46(5), pp.853-856

1998

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A total synthesis of magallanesine via [1, 2]-Meisenheimer rearrangement

Tetrahedron letters, 1994-05, Vol.35 (22), p.3749-3752

1994

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Efficient and β-Stereoselective Synthesis of 4(5)-Methyl-5(4)-(5-amino-5-deoxy-β-D-ribofuranosyl)imidazole and Related Compounds Exhibiting Antiulcer Activity

Chemical and Pharmaceutical Bulletin, 1997/01/15, Vol.45(1), pp.53-61

1997

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[3,3]Sigmatropic ring expansion of cyclic thionocarbonates. 12. synthesis of (−)-yellow scale pheromone

Tetrahedron, 1993, Vol.49 (46), p.10577-10586

1993

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Synthesis of medium-membered heterocyclic allenes by [3,3]sigmatropic rearrangement and its synthetic application to the antifungal constituent of sapium japonicum

Tetrahedron letters, 1994-02, Vol.35 (8), p.1255-1258

1994

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Synthesis of C-Ring Modified Analogues of Camptothecin

Heterocycles, 1997, Vol.46 (1), p.357

1997

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[3,3]Sigmatropic ring expansion of cyclic thionocarbonates. 9. total synthesis of (±)-yellow scale pheromone via 10-membered thiolcarbonate

Tetrahedron, 1993-08, Vol.49 (35), p.7657-7666

1993

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Cyanophosphate: An efficient intermediate for conversion of carbonyl compounds to nitriles

Tetrahedron letters, 1989, Vol.30 (28), p.3681-3684

1989

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Intracerebroventricular administration of histamine H3 receptor antagonists decreases seizures in rat models of epilepsia

Design and synthesis of an aminobenzo-15-crown-5-labeled estradiol tethered with disulfide linkage

Nucleobase Participation in Ribozyme Catalysis

A Selective Human H 4 -Receptor Agonist: (−)-2-Cyano-1-methyl-3-{(2 R ,5 R )-5- [1 H -imidazol-4(5)-yl]tetrahydrofuran-2-yl}methylguanidine

Efficient and β-Stereoselective Synthesis of Pyrazole C-Nucleosides

Synthesis of novel C4-linked imidazole ribonucleoside phosphoramidites for probing general acid and base catalysis in ribozyme

Accurate molecular weight measurements of nucleoside phosphoramidites: a suitable matrix of mass spectrometry

(13-Methyl-1,4,7,8,13,13b-hexahydro[1',2']oxazepino[2',3':1,2]pyrido[3,4-b]indol-1-yl)methanol and its Unusual Packing Style

Efficient and beta-Stereoselective Synthesis of 4(5)-(beta-D-Ribofuranosyl)- and 4(5)-(2-Deoxyribofuranosyl)imidazoles(1)

Formation of Two 4-Imidazolylmethylphosphonium Salts and their Synthetic Studies Toward Histamine H 3 -Ligands

An efficient synthesis of magallanesine using [1,2]-Meisenheimer rearrangement and Heck cyclization

Synthesis of imifuramine and its stereoisomers exhibiting histamine H 3-agonistic activity

Synthesis of 4(5)-(a-D-Xylofuranosyl)imidazole Starting from L-Arabinose: Mitsunobu Cyclization via C4’-Oxyphosphonium Intermediate

Cyano phosphate: an efficient intermediate for the chemoselective conversion of carbonyl compounds to nitriles

Stereoselective synthesis of the C-4 linked imidazole nucleosides using modified Mitsunobu reaction

A synthesis of taxusin

Synthesis of an indole analog of magallanesine via the [1,2]-meisenheimer rearrangement

Studies on the [2, 3]-Meisenheimer Rearrangement of 2-Vinylazetidine N-Oxides

A total synthesis of magallanesine via [1, 2]-Meisenheimer rearrangement

Efficient and β-Stereoselective Synthesis of 4(5)-Methyl-5(4)-(5-amino-5-deoxy-β-D-ribofuranosyl)imidazole and Related Compounds Exhibiting Antiulcer Activity

[3,3]Sigmatropic ring expansion of cyclic thionocarbonates. 12. synthesis of (−)-yellow scale pheromone

Synthesis of medium-membered heterocyclic allenes by [3,3]sigmatropic rearrangement and its synthetic application to the antifungal constituent of sapium japonicum

Synthesis of C-Ring Modified Analogues of Camptothecin

[3,3]Sigmatropic ring expansion of cyclic thionocarbonates. 9. total synthesis of (±)-yellow scale pheromone via 10-membered thiolcarbonate

Cyanophosphate: An efficient intermediate for conversion of carbonyl compounds to nitriles

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