Zobrazeno 1 - 10
of 321
pro vyhledávání: '"Shunichi Hashimoto"'
Autor:
Masahiro Anada, Shunichi Hashimoto
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 77:553-565
Autor:
Shunichi Hashimoto, Takao Nomura, Katsumi Maenaka, Masahiro Anada, Hisanori Nambu, Naoyoshi Maeda, Hisashi Arase, Mikihiro Ishizuka, Nanao Hatori, Shigeki Matsunaga, Atsushi Furukawa, Kimiko Kuroki, Jiro Sakamoto, Fumina Ohsaka, Tomoki Yamada, Toyoyuki Ose, Takashi Saitoh, Kosuke Kakita
Publikováno v:
Journal of Biological Chemistry. 292(51):21128-21136
金沢大学医薬保健研究域薬学系
Before entering host cells, herpes simplex virus-1 uses its envelope glycoprotein B to bind paired immunoglobulin-like type 2 receptor α (PILRα) on immune cells. PILRα belongs to the Siglec (sialic a
Before entering host cells, herpes simplex virus-1 uses its envelope glycoprotein B to bind paired immunoglobulin-like type 2 receptor α (PILRα) on immune cells. PILRα belongs to the Siglec (sialic a
Autor:
Yasunobu Kurosaki, Taiki Hanari, Yu Jinushi, Koji Takeda, Kosuke Kakita, Yuta Sunadoi, Shunichi Hashimoto, Masahiro Anada, Shigeki Matsunaga, Kazuki Katsuse
Publikováno v:
Organic Letters. 19:5581-5584
The first total synthesis of brasilicardins A and C, novel diterpenoid-saccharide-amino acid hybrid metabolites with unique immunosuppressive activity, is described. The key step is a Diels-Alder/reductive angular methylation sequence capitalizing on
Publikováno v:
ISIJ International. 57:945-952
Autor:
Shunichi Hashimoto, Masahiro Anada, Motoki Ito, Yuji Kondo, Ryosuke Namie, Yoshihiro Natori, Koji Takeda, Hisanori Nambu, Yasunori Yamamoto
Publikováno v:
HETEROCYCLES. 103:1078
Autor:
Kazushi Minami, Motoki Ito, Shunichi Hashimoto, Masahiro Anada, Shigeki Matsunaga, Taku Miyazawa
Publikováno v:
Tetrahedron. 72:3939-3947
The first enantio-and diastereoselective construction of fused bicyclic ring systems via intramolecular C–H insertion reaction of σ-symmetric α-alkyl-α-diazoesters is described. With dirhodium(II) tetrakis[N-phthaloyl-(S)-tert-leucinate], Rh2(S-
Publikováno v:
Tetsu-to-Hagane. 102:525-533
Publikováno v:
Tetrahedron Letters. 56:4324-4327
An asymmetric synthesis of (−)-E-δ-viniferin, a trans-resveratrol dimer natural product containing a dihydrobenzofuran ring, has been achieved by exploiting a Rh(II)-catalyzed intramolecular C–H insertion reaction of a diaryldiazomethane derivat
Publikováno v:
Tetrahedron Letters. 56:1397-1400
The first catalytic asymmetric intramolecular 1,6-C–H insertion reaction of α-diazo esters is described. With dirhodium(II) tetrakis[N-phthaloyl-(S)-tert-leucinate], Rh2(S-PTTL)4, the C–H insertion proceeded in a chemoselective manner to give 2-
Publikováno v:
Organic Letters. 16:2054-2057
A stereoselective synthesis of the CDE ring portion of the antitumor saponin scillascilloside E-1 has been achieved, utilizing an Ireland-Claisen rearrangement to construct the contiguous tetrasubstituted stereocenters at C13 and C17 simultaneously a