Zobrazeno 1 - 10
of 25
pro vyhledávání: '"David S. Hays"'
Autor:
Kyle J. Lindstrom, Philip D. Heppner, Daniel J Willie, Michael E. Danielson, Charles M. Leir, Joshua R. Wurst, Gregory D. Lundquist, Sonja S. Mackey, Tushar A. Kshirsagar, Chad A. Haraldson, David S. Hays, Karl E. Benson
Publikováno v:
The Journal of Organic Chemistry. 72:4570-4573
The deprotonation and regioselective reaction of 2H-pyrazolo[3,4-c]quinolines with a variety of electrophiles is described. Electrophiles include benzaldehyde, DMF, carbon dioxide, and iodine. This method provides a direct route to a class of pharmac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b0237f06064236349491db0ad2186ef
https://doi.org/10.1021/jo070392t
https://doi.org/10.1021/jo070392t
Autor:
David S. Hays, Gregory C. Fu
Publikováno v:
Tetrahedron. 55:8815-8832
By sequencing two known reactions, a new catalytic carbon-carbon bond-forming process, the Bu 3 SnH-catalyzed, PhSiH 3 -mediated reductive cyclization of enals and enones, has been developed. The addition of EtOH to the reactions leads to reproducibl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61a2ba6dc42bff8bd0917419bdd4579c
https://doi.org/10.1016/s0040-4020(99)00446-9
https://doi.org/10.1016/s0040-4020(99)00446-9
Autor:
Gregory C. Fu, David S. Hays
Publikováno v:
The Journal of Organic Chemistry. 63:6375-6381
A new method is described for the intramolecular pinacol coupling of 1,5- and 1,6-dicarbonyl compounds, employing Bu(3)SnH as the stoichiometric reductant. The key steps in this pinacol cyclization are the addition of a tin ketyl to a carbonyl group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc19f7c68f6948115bfeff4b63d7dfdc
https://doi.org/10.1021/jo9809130
https://doi.org/10.1021/jo9809130
Publikováno v:
The Journal of Organic Chemistry. 60:1391-1407
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31d60ce02a7c5b8596946c5b00d52661
https://doi.org/10.1021/jo00110a049
https://doi.org/10.1021/jo00110a049
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee5a398f4bce50f66517673150d865cd
https://doi.org/10.1002/chin.199535068
https://doi.org/10.1002/chin.199535068
Autor:
Gregory C. Fu, David S. Hays
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b20e2f330f781ada2200a882ed209012
https://doi.org/10.1002/chin.199545064
https://doi.org/10.1002/chin.199545064
Autor:
Gregory C. Fu, David S. Hays
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed14508fa3208920545db4d85d39b787
https://doi.org/10.1002/chin.199620051
https://doi.org/10.1002/chin.199620051
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b736c8881930948ef377dc786d325aaa
https://doi.org/10.1002/chin.199706057
https://doi.org/10.1002/chin.199706057
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::448ebdf73c450caa4552bcb0f63799bb
https://doi.org/10.1002/chin.199744063
https://doi.org/10.1002/chin.199744063
Autor:
Gregory C. Fu, David S. Hays
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99050954bae26ba52bcb35206f9f8834
https://doi.org/10.1002/chin.199809177
https://doi.org/10.1002/chin.199809177