Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Hiromi Ohtomo"'
Publikováno v:
Journal of Heterocyclic Chemistry. 48:715-719
N-[2-([1,2,4]Oxadiazol-5-yl)cyclohepten-1-yl]formamide oximes were synthesized by fusion of (6,7,8,9-tetrahydro-5H-cyclohepta[1,2-d]pyrimidin-4-yl)amidines with hydroxylamine hydrochloride through a subsequent rearrangement reaction. Effects of the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::902cbd08910e705283c3b37c55fff08d
https://doi.org/10.1002/jhet.564
https://doi.org/10.1002/jhet.564
Publikováno v:
Synthetic Communications. 41:812-819
The reaction of 3-(2-bromoethyl)quinazolin-4(3H)-one with ethyl- and n-propylamine gave abnormal fused 3-alkyl-4-alkyliminoquinazolines via a Dimroth-type rearrangement, as well as normal substituted 3-(2-alkylaminoethyl) derivatives in methanol. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b501289ab9b3799f0d87d4a7b810fa5
https://doi.org/10.1080/00397911003668570
https://doi.org/10.1080/00397911003668570
Publikováno v:
Chemical and Pharmaceutical Bulletin. 57:755-758
Reaction of some fused tricyclic 3-(2-bromoethyl)pyrimidin-4(3H)-ones with primary alkyl amines gave abnormal fused 3-alkyl-4-alkyliminopyrimidines via a Dimroth-type rearrangement, as well as normal substituted 3-(2-alkylaminoethyl) derivatives in m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77113480a52ea19c8bcafe4159928f23
https://doi.org/10.1248/cpb.57.755
https://doi.org/10.1248/cpb.57.755
Publikováno v:
Tetrahedron. 63:12541-12546
Reaction of fused 3-(2-bromoethyl)pyrimidin-4(3H)-ones with primary alkylamines gave abnormal fused 3-alkyl-4-alkyliminopyrimidines via a new rearrangement, as well as normal substituted 3-(2-alkylaminoethyl) derivatives. Antidepressive evaluation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b76db4614ec29cd758c64566d999073d
https://doi.org/10.1016/j.tet.2007.10.024
https://doi.org/10.1016/j.tet.2007.10.024
Publikováno v:
Journal of Heterocyclic Chemistry. 33:1663-1669
Synthesis of 11-substituted 1,2,4,5-tetrahydrobenzo[h]imidazo[1,2-c]quinazolines corresponding to 12-substituted 11,13,15-triazasteroid is described. Evaluation on inhibitory activity against collagen-induced platelet aggregation of these compounds a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fcb0d2a8bfc56a232bee1b35089cae2
https://doi.org/10.1002/jhet.5570330619
https://doi.org/10.1002/jhet.5570330619
Publikováno v:
ChemInform. 42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14feea208ad47cd1d0a5040f532fb994
https://doi.org/10.1002/chin.201142131
https://doi.org/10.1002/chin.201142131
Publikováno v:
ChemInform. 42
The reaction of quinazolinone or tetrahydroquinazolinone derivatives of type (II) with alkylamines gives 3-alkyl-4-alkylimino compounds of type (IV) via a Dimroth-type rearrangement or normal substitution products of type (V).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f7e01ebaff2f72b8f33133694534847
https://doi.org/10.1002/chin.201132158
https://doi.org/10.1002/chin.201132158
Publikováno v:
Journal of Heterocyclic Chemistry. 30:989-992
Synthesis of benzo[3,4]cyclohepta[1,2-e]pyrimido[1,2-c]pyrimidines, corresponding to the B,D-dihomo-11,13,15-triazasteroidal skeleton as a novel ring system is described. Their effects on reserpine-induced hypothermia in mice and inhibitory activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::855a472bfd9db9fc29b12414ba1d9038
https://doi.org/10.1002/jhet.5570300425
https://doi.org/10.1002/jhet.5570300425
Autor:
Hiromi Ohtomo, Yoshiji Hantani, Minoru Yamada, Tomohisa Nagamatsu, Takashi Hirota, Taiji Nakayama, Kenji Sasaki
Publikováno v:
Journal of Heterocyclic Chemistry. 30:193-202
As a series of polyheterocyclic compounds for exploitation as anti-platelet agents, tricyclic heterocyclic compounds, 4-substituted 6,7-dihydro-5H-pyrimido[5,4-d][1]benzazepines 3–6, 9, 12–14, and 16–26, having nitrogen, oxygen, or sulfur conta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfb174ebea4ebd2ceaa3dd856d6c7442
https://doi.org/10.1002/jhet.5570300134
https://doi.org/10.1002/jhet.5570300134
Autor:
Kenji Sasaki, Tomohisa Nagamatsu, Yoshiji Hantani, Hiromi Ohtomo, Taiji Nakayama, Takashi Hirota
Publikováno v:
Journal of Heterocyclic Chemistry. 30:233-240
A study of the cyclization method by heating of N-(6,7-dihydro-5H-pyrimido[5,4-d][1]benzazepin-4-yl)amino acids 3a-h, 6, and 9a,b with excess acetic anhydride for the preparation of 2-substituted 1-acetoxy-6-acetyl-5,6-dihydro-4H-imidazo[1,2′:1,6]p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4192f12df07a88553a0539d55ecc3d74
https://doi.org/10.1002/jhet.5570300140
https://doi.org/10.1002/jhet.5570300140