Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kaoru, Inada"'
Autor:
Hiroshi, Ueda, Shingo, Nakamura, Taro, Nakamura, Kaoru, Inada, Takashi, Okubo, Naohiro, Furukawa, Reiichi, Murakami, Shigeo, Tsuchida, Yonathan, Zohar, Kotaro, Konno, Masahiko, Watanabe
Publikováno v:
Scientific Reports
The olfactory hypothesis for salmon imprinting and homing to their natal stream is well known, but the endocrine hormonal control mechanisms of olfactory memory formation in juveniles and retrieval in adults remain unclear. In brains of hatchery-rear
Autor:
Norio Miyaura, Kaoru Inada
Publikováno v:
Tetrahedron. 56:8657-8660
The cross-coupling reaction of tolylboronic acids (1.3 equiv.) with chloroarenes in toluene was carried out at 80–100°C in the presence of a NiCl2/PPh3 catalyst (3 mol%) and K3PO4·nH2O (2.6 equiv.). The reaction can be applied to various electron
Autor:
Kaoru Inada, Norio Miyaura
Publikováno v:
Tetrahedron. 56:8661-8664
The cross-coupling reaction of tolylboronic acids (1.3 equiv.) with chloropyridines, chloroquinoline, or activated chloroarenes having an electron-withdrawing group was carried out in toluene at 80°C in the presence of a polymer-bound PdCl 2 catalys
Autor:
Masahiko Watanabe, Reiichi Murakami, Kaoru Inada, Shingo Nakamura, Takashi Okubo, Taro Nakamura, Kotaro Konno, Hiroshi Ueda, Yonathan Zohar, Naohiro Furukawa, Shigeo Tsuchida
Publikováno v:
Scientific reports. 6:21102
The olfactory hypothesis for salmon imprinting and homing to their natal stream is well known, but the endocrine hormonal control mechanisms of olfactory memory formation in juveniles and retrieval in adults remain unclear. In brains of hatchery-rear
Autor:
Norio Miyaura, Kaoru Inada
Publikováno v:
ChemInform. 32
The cross-coupling reaction of tolylboronic acids (1.3 equiv.) with chloropyridines, chloroquinoline, or activated chloroarenes having an electron-withdrawing group was carried out in toluene at 80°C in the presence of a polymer-bound PdCl 2 catalys
Autor:
Norio Miyaura, Kaoru Inada
Publikováno v:
ChemInform. 32
The cross-coupling reaction of tolylboronic acids (1.3 equiv.) with chloroarenes in toluene was carried out at 80–100°C in the presence of a NiCl2/PPh3 catalyst (3 mol%) and K3PO4·nH2O (2.6 equiv.). The reaction can be applied to various electron