Zobrazeno 1 - 8
of 8
pro vyhledávání: '"P. L. Nyce"'
Autor:
Ashit K. Ganguly, S. Rosenhouse, John K. Jenkins, Viyyoor M. Girijavallabhan, Stuart W. McCombie, D. Gala, P. L. Nyce, M. Steinman, John S. Chiu, R. S. Jaret
Publikováno v:
ChemInform. 23
A synthesis of penems from azetidinone 1 is described in detail. This synthesis is used to prepare multikilo batches of (5R,6S)-2-[[-(carbamoyloxy)ethyl]thio]-6-[(R)-1-hydroxyethyl]penem-3-carboxylic acid (10), (Sch 34343). It is practical as all che
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63a13a955df3610c85a593c590798131
https://doi.org/10.1002/chin.199221303
https://doi.org/10.1002/chin.199221303
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16fed0879f92605d829182e13a869c5e
https://doi.org/10.1002/chin.199149186
https://doi.org/10.1002/chin.199149186
Autor:
P. L. Nyce, Stuart W. McCombie, D. Gala, Ashit K. Ganguly, S. Rosenhouse, John K. Jenkins, Viyyoor M. Girijavallabhan, M. Steinman, John S. Chiu, R. S. Jaret
Publikováno v:
Tetrahedron. 48:1175-1182
A synthesis of penems from azetidinone 1 is described in detail. This synthesis is used to prepare multikilo batches of (5R,6S)-2-[[-(carbamoyloxy)ethyl]thio]-6-[(R)-1-hydroxyethyl]penem-3-carboxylic acid (10), (Sch 34343). It is practical as all che
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee79c09a9bb06179043409270dd7386d
https://doi.org/10.1016/s0040-4020(01)90781-1
https://doi.org/10.1016/s0040-4020(01)90781-1
Publikováno v:
Synthesis. 1991:571-574
A new, efficient synthesis of 1,8-naphthyridin-2(1H)-ones as applied to the synthesis of the leukotriene release inhibitor, 1,2-dihydro-1-phenyl-3-pyrrolidinio-2-oxo-1,8-naphthyridin-4-olate inner salt (4) from methyl 2-phenylamino-3-pyridinecarboxyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d7f288a48d71e34d760476a993a0aa8
https://doi.org/10.1055/s-1991-26519
https://doi.org/10.1055/s-1991-26519
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09a4fc46f54ac16eeb9c4c04cd43c918
https://doi.org/10.1002/chin.199050149
https://doi.org/10.1002/chin.199050149
Publikováno v:
Synlett. 1990:431-432
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fd9df06486167d3867525914149f1eb
https://doi.org/10.1055/s-1990-21119
https://doi.org/10.1055/s-1990-21119
Publikováno v:
Journal of Heterocyclic Chemistry. 24:505-508
Addition de l'ethylcetene (forme par reaction du chlorure de butyryle et de triethylamine) sur le phenyl-5 oxazole et la methyl-5 tosyl-4 oxazoline: obtention des derives butyryloxy-1' butene-1' yl-2. Etude RMN; mecanisme de l'addition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbb813a53b2e9c7536213f4f366dca90
https://doi.org/10.1002/jhet.5570240239
https://doi.org/10.1002/jhet.5570240239
Publikováno v:
ChemInform. 18
Addition de l'ethylcetene (forme par reaction du chlorure de butyryle et de triethylamine) sur le phenyl-5 oxazole et la methyl-5 tosyl-4 oxazoline: obtention des derives butyryloxy-1' butene-1' yl-2. Etude RMN; mecanisme de l'addition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::280ca47d49a16efcbc034fbf4ba11517
https://doi.org/10.1002/chin.198746195
https://doi.org/10.1002/chin.198746195