Zobrazeno 1 - 10
of 19
pro vyhledávání: '"T. P. Selby"'
Publikováno v:
ACS Symposium Series ISBN: 9780841218857
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85a89040dac60a13b42c91aa0d61fe30
https://doi.org/10.1021/bk-1991-0443.ch006
https://doi.org/10.1021/bk-1991-0443.ch006
Autor:
T. P. Selby, B. K. Smith
Publikováno v:
ChemInform. 21
Condensation of 2-amino-4-hydroxy-2-mercaptopyrimidine (2) hydrate and ethyl 4-bromocrotonate gave a mixture of ethyl 7-amino-2,3-dihydro-5-oxo-5H-thiazolo [3,2-a] pyrimidine-3-acetate (4) and 2a,3-dihydro-1-thia-5,8,8b-triazaacenaphthylene-4,7(2H)-d
Autor:
T. P. Selby, E. Campaigne
Publikováno v:
Journal of Heterocyclic Chemistry. 15:401-411
By varying the acidity, solvent polarity, and temperature when thiosemicarbazide reacted with ethyl 4-chloroacetoacetate, ethyl 2-amino-6H-1,3,4-thiadiazine-5-acetate hydrochloride, ethyl 2-hydrazinothiazole-4-acetate, and ethyl 2-imino-3-aminothiazo
Publikováno v:
Journal of Heterocyclic Chemistry. 16:725-729
Condensation of ethyl 4-chloroacetoacetate with 4-amino-6-hydroxy-2-pyrimidinethiol produced ethyl 3-hydroxy-5-amino-7-oxothiazolino[3,2-a]pyrimidin-3-acetate (7a) on crystallization. Subsequent ring closure of 7a produced the tricyclic 6a-hydroxy-5,
Autor:
G. E. Lepone, T. P. Selby
Publikováno v:
Journal of Heterocyclic Chemistry. 21:61-64
Previously it was shown that condensation of dimethyl N-cyanodithioimidocarbonate (1a) with methylhydrazine gave predominantly 1-methyl-5-methylthio-1H-,2,4-triazol-3-amine (2), which was initially identified erroneously as the regioisomer l-methyl-3
Autor:
E. Campaigne, T. P. Selby
Publikováno v:
Journal of Heterocyclic Chemistry. 16:151-156
A unique covalently hydrated cyclazine adduct, 2-imino-6a-hydroxy-4,5,6,6a-tetrahydro-7H-8-thia-J, 4-diazacycl[3.3.2]azin-5-one hydrochloride was prepared by reacting ethyl 4-chloro-acetoacetate with 4,6-diamino-2-thiopyrimidine in neutral alcohol. N
Autor:
B. K. Smith, T. P. Selby
Publikováno v:
Journal of Heterocyclic Chemistry. 26:1237-1240
Condensation of 2-amino-4-hydroxy-2-mercaptopyrimidine (2) hydrate and ethyl 4-bromocrotonate gave a mixture of ethyl 7-amino-2,3-dihydro-5-oxo-5H-thiazolo [3,2-a] pyrimidine-3-acetate (4) and 2a,3-dihydro-1-thia-5,8,8b-triazaacenaphthylene-4,7(2H)-d
Publikováno v:
Journal of Heterocyclic Chemistry. 18:575-580
Ethyl 4-chloroacetoacetate condenses with 4-amino-6-hydroxy-2-pyrimidinethiol to yield ethyl 3-hydroxy-5-oxo-7-aminothiazolino[3,2-a]pyrimidin-3-acetate (3), and not ethyl 3-hydroxy-5-amino-7-oxothiazolino[3,2-a]-pyrimidin-3-acetate, as previously re
Autor:
E. Campaigne, T. P. Selby
Publikováno v:
Journal of Heterocyclic Chemistry. 17:1249-1253
Nitrosation of hydrazino substituted thiazole-4-acetates has been shown to occur on the ring, rather than the α-methylene carbon, as previously reported. Thus nitrosation of ethyl 2-isopropylidenehydrazono-, 2-benzylidenehydrazono-, 2-(2-benzoylhydr
Autor:
T. P. Selby, E. Campaigne
Publikováno v:
Journal of Heterocyclic Chemistry. 17:1255-1257