Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ryoichi Okuda"'
Autor:
Michiaki Hashimoto, Izumi Watadani, Ryoichi Okuda, Yasuyuki Fujiwara, Hideki Okamoto, Masaru Kimura, Kyosuke Satake, Shiro Morosawa
Publikováno v:
ChemInform. 23
Demethoxycarbonylation of methyl 2,5,-di-tert-butyl-1H-azepine-1-carboxylate using 1,8-diazabicyclo[5.4.0]undec-7-ene gives exclusively two isomers of 3H-azepine derivatives, while methyl 3,6-di-tert-butyl-1H-azepine-1-carboxylate gives a mixture of
Autor:
Ryoichi Okuda, Hideki Okamoto, Michiaki Hashimoto, Kyosuke Satake, Yasuyuki Fujiwara, Shiro Morosawa, Masaru Kimura
Publikováno v:
ChemInform. 25
Demethoxycarbonylation of methyl 2,5-di-tert-butyl-1H-azepine-1-carboxylate using 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) gave 3H-azepines. Under similar conditions, methyl 3,6-di-tert-butyl-1H-azepine-1-carboxylate gave not only the 3H-azepine but
Autor:
Ryoichi Okuda, Masaru Kimura, Kyosuke Satake, Michiaki Hashimoto, Yasuyuki Fujiwara, Shiro Morosawa, Hideki Okamoto
Publikováno v:
Scopus-Elsevier
Demethoxycarbonylation of methyl 2,5-di-tert-butyl-1H-azepine-1-carboxylate using 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) gave 3H-azepines. Under similar conditions, methyl 3,6-di-tert-butyl-1H-azepine-1-carboxylate gave not only the 3H-azepine but
Autor:
Masaru Kimura, Ryoichi Okuda, Kyosuke Satake, Shiro Morosawa, Yasuyuki Fujiwara, Michiaki Hashimoto, Izumi Watadani, Hideki Okamoto
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :1154
Demethoxycarbonylation of methyl 2,5,-di-tert-butyl-1H-azepine-1-carboxylate using 1,8-diazabicyclo[5.4.0]undec-7-ene gives exclusively two isomers of 3H-azepine derivatives, while methyl 3,6-di-tert-butyl-1H-azepine-1-carboxylate gives a mixture of