H. Hamaguchi

发表

Palladium(0)-catalyzed synthesis of medium-sized heterocycles by using bromoallenes as an allyl dication equivalent.

H. Ohno, H. Hamaguchi, Miyo Ohata, 2004, Journal of the American Chemical Society.

Discovery and structural characterization of peficitinib (ASP015K) as a novel and potent JAK inhibitor.

K. Nakai, Ayako Moritomo, Takayuki Inoue, 2018, Bioorganic & medicinal chemistry.

Discovery of 3,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridin-2(1H)-one derivatives as novel JAK inhibitors.

A. Tanaka, Ayako Moritomo, Takayuki Inoue, 2015, Bioorganic & medicinal chemistry.

Synthesis and evaluation of novel 1H-pyrrolo[2,3-b]pyridine-5-carboxamide derivatives as potent and orally efficacious immunomodulators targeting JAK3.

A. Tanaka, K. Nakai, Ayako Moritomo, 2015, Bioorganic & medicinal chemistry.

Palladium(0)-catalyzed tandem cyclization of allenenes: direct construction of tricyclic heterocycles through aromatic C--H activation.

H. Ohno, H. Hamaguchi, Tetsuaki Tanaka, 2005, Chemistry.

2-ethynylaziridines as chiral carbon nucleophiles: stereoselective synthesis of 1,3-amino alcohols with three stereocenters via allenylindium reagents bearing a protected amino group.

H. Ohno, H. Hamaguchi, T. Tanaka, 2001, The Journal of organic chemistry.

Stereoselective synthesis of chiral 2,3-cis-2-ethynylaziridines by base-mediated intramolecular amination of bromoallenes.

H. Ohno, H. Hamaguchi, Tetsuaki Tanaka, 2001, Organic letters.

Umpolung of Chiral 2‐Ethynylaziridines: Indium(I)‐Mediated Stereoselective Synthesis of Nonracemic 1,3‐Amino Alcohols Bearing Three Chiral Centers, Catalyzed by Palladium(0).

H. Ohno, H. Hamaguchi, Tetsuaki Tanaka, 2000 .

Novel Synthesis of Azocine, Azepine, Oxocine, and Oxepine Derivatives by Palladium-catalyzed Medium-Ring Formation from Bromoallenes

H. Ohno, H. Hamaguchi, Miyo Ohata, 2003 .

Bromoallenes as allyl dication equivalents in the presence or absence of palladium(0): direct construction of bicyclic sulfamides containing five- to eight-membered rings by tandem cyclization of bromoallenes.

N. Fujii, H. Ohno, H. Hamaguchi, 2007, Chemistry.

Bromoallenes as allyl dication equivalents in the absence of palladium(0): synthesis of bicyclic sulfamides by tandem cyclization of bromoallenes.

H. Ohno, H. Hamaguchi, Shohei Kosaka, 2005, Angewandte Chemie.

Umpolung of chiral 2-ethynylaziridines: Indium(I)-mediated stereoselective synthesis of nonracemic 1,3-amino alcohols bearing three chiral centers, catalyzed by palladium(0)

Ohno, H. Ohno, H. Hamaguchi, 2000, Organic letters.

Bromoallenes as synthetic equivalents of allyl dications: synthesis of medium-sized nitrogen heterocycles through the cyclization of bromoallenes in the presence of a palladium(0) catalyst and an alcohol.

H. Ohno, H. Hamaguchi, Miyo Ohata, 2003, Angewandte Chemie.

A highly cis-selective synthesis of 2-ethynylaziridines by intramolecular amination of chiral bromoallenes: improvement of stereoselectivity based on the computational investigation.

H. Ohno, K. Ando, H. Hamaguchi, 2002, Journal of the American Chemical Society.

Novel quinuclidinyl heteroarylcarbamate derivatives as muscarinic receptor antagonists.

M. Takeuchi, T. Kontani, Ayako Moritomo, 2014, Bioorganic & medicinal chemistry.