Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Yasuharu Shimasaki"'
Autor:
Yasuharu Shimasaki, Yumi Hayashi, Yosuke Tomioka, Toshiaki Aikawa, Takashi Miki, Hiroaki Okamoto, Tetsuya Ikemoto, Masahiro Takeda
Publikováno v:
Organic Process Research & Development. 20:1615-1620
An efficient method for synthesizing 1-({[(3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yloxy]carbonyl}oxy)pyrrolidine-2,5-dione (1), a key building block for HIV protease inhibitors, has been developed. A diphenylprolinol-catalyzed highly enantio- and di
Formal Synthesis of Ezetimibe Using a Proline-mediated, Asymmetric, Three-component Mannich Reaction
Publikováno v:
Chemistry Letters. 45:30-32
The formal total synthesis of ezetimibe was accomplished using a proline-mediated, asymmetric, three-component Mannich reaction as the key step. The two stereogenic centers on the β-lactam skeleton...
Autor:
Theresa Humphries, Takashi Miki, Qingping Tian, Scott Savage, Zhigang Cheng, Yasuharu Shimasaki, Norihiko Hirata, Mark Reynolds, Mitsuhiro Iwasaki, Srinivasan Babu, David Askin, Francis Gosselin, Herbert Yajima, Keena Green, Isao Kurimoto
Publikováno v:
Organic Process Research & Development. 17:97-107
We report a practical synthesis of PI3K inhibitor GDC-0941. The synthesis was achieved using a convergent approach starting from a thienopyrimidine intermediate through a sequence of formylation and reductive amination followed by Suzuki-Miyaura cros
Autor:
Osamu Nakayama, Yasuharu Shimasaki, Shigefumi Kuwahara, Masatoshi Saitoh, Hiromasa Kiyota, Tomoko Takada, Takafumi Takai
Publikováno v:
Synthesis. 2007:2471-2480
Synthesis of (-)-tabtoxinine-b-lactam and its (3R)-iso- mer, the cause of tobacco wildfire disease, was achieved from L- serine using a zinc-mediated coupling reaction, Sharpless asymmet- ric dihydroxylation and lactamization of b-mesyloxy benzylhy-
Publikováno v:
Tetrahedron. 62:9628-9634
(S)-Gizzerosine, a potent inducer of gizzard erosion in chicks, was synthesized using successive zinc-mediated and palladium-catalyzed coupling reactions as the key steps.
Publikováno v:
ChemInform. 38
Publikováno v:
ChemInform. 37
Gizzerosine, a potent inducer of gizzard erosion in chicks, was synthesized using successive zinc-mediated and palladium-catalyzed coupling reactions as the key steps. The piperonyl moiety was used as a novel N-protectinggroup.
Autor:
Yumi Hayashi, Toshiaki Aikawa, Yasuharu Shimasaki, Hiroaki Okamoto, Yosuke Tomioka, Takashi Miki, Masahiro Takeda, Tetsuya Ikemoto
Publikováno v:
Organic Process Research & Development; Sep2016, Vol. 20 Issue 9, p1615-1620, 6p
Autor:
Hiromasa Kiyota, Takafumi Takai, Yasuharu Shimasaki, Masatoshi Saitoh, Osamu Nakayama, Tomoko Takada, Shigefumi Kuwahara
Publikováno v:
Synthesis; 2007, Vol. 2007 Issue 16, p2471-2480, 10p