Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Masaaki Imasho"'
Synthetic studies on the starfish alkaloid imbricatine. Construction of an ent-imbricatine framework
Publikováno v:
Chemical & pharmaceutical bulletin. 47(1):83-89
A chiral synthetic route to the amino esters 5 and 6, which contain the fundamental framework of ent-imbricatine (ent-3), has been developed as a prelude to the total synthesis of the starfish alkaloid imbricatine (3). The route started from the sulf
Autor:
Raymond J. Andersen, Masashi Ohba, Masaaki Imasho, Julia Kubanek, Tatsuya Fujii, Yoshikazu Nishimura
Publikováno v:
Tetrahedron Letters. 39:5999-6002
A chiral synthesis of tri- O -methylimbricatine ( 2 ), the tri- O -methyl derivative of the unique benzyltetrahydroisoquinoline alkaloid imbricatine ( 1 ) isolated from the starfish Dermasterias imbricata , has been accomplished. As a result of the s
Publikováno v:
ChemInform. 27
Autor:
Julia Kubanek, Masaaki Imasho, Yoshikazu Nishimura, Tatsuya Fujii, Raymond J. Andersen, Masashi Ohba
Publikováno v:
ChemInform. 29
A chiral synthesis of tri- O -methylimbricatine ( 2 ), the tri- O -methyl derivative of the unique benzyltetrahydroisoquinoline alkaloid imbricatine ( 1 ) isolated from the starfish Dermasterias imbricata , has been accomplished. As a result of the s
Publikováno v:
ChemInform. 30
A chiral synthetic route to the amino esters 5 and 6, which contain the fundamental framework of ent-imbricatine (ent-3), has been developed as a prelude to the total synthesis of the starfish alkaloid imbricatine (3). The route started from the sulf
Autor:
Masaaki Imasho, Yoshiyuki Tsumamoto, Mohammad Ali, Shinzo Hosoi, Fumiyuki Kiuchi, Yoshisuke Tsuda, Youhei Sasaki, Eriko Tanaka, Norio Nakamura, Kaoru Kondo
Publikováno v:
Chemicalpharmaceutical bulletin. 47(1)
Twenty diarylnonanones were synthesized and their nematocidal activity was examined. Among those, the p-hydroxy compound 16 exhibited the strongest activity comparable to the natural diarylnonanoids, malabaricones A and C. Diarylundecanoid 57 also sh
Publikováno v:
HETEROCYCLES. 42:219