Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Thomas J. Laughlin"'
Autor:
David F. Savage, Benjamin L. Oakes, Rachel J. Lew, Christof Fellmann, Madeline L. Arnold, Maria Lukarska, Brett T. Staahl, Sean Higgins, Jennifer A. Doudna, Arik Shams, Thomas J. Laughlin
Proteins evolve through the modular rearrangement of elements known as domains. It is hypothesized that extant, multidomain proteins are the result of domain accretion, but there has been limited experimental validation of this idea. Here, we introdu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1f66e6e83764defec213e57cff04e32
https://doi.org/10.1101/2020.10.19.344077
https://doi.org/10.1101/2020.10.19.344077
Bismuth(III) bromide catalyzed synthesis of polyhydroquinoline derivatives via the Hantzsch reaction
Publikováno v:
Tetrahedron Letters. 56:4060-4062
Bismuth(III) bromide is an efficient catalyst for the one-pot multicomponent synthesis of polyhydroquinolines via the Hantzsch reaction. The mild reaction conditions, short reaction times, high yields, and the remarkably low toxicity of bismuth compo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f64cb17d6dbfa6d080cc9afae3dd5454
https://doi.org/10.1016/j.tetlet.2015.04.121
https://doi.org/10.1016/j.tetlet.2015.04.121
Publikováno v:
ChemInform. 46
Bismuth(III) bromide is an efficient catalyst for the one-pot multicomponent synthesis of polyhydroquinolines via the Hantzsch reaction. The mild reaction conditions, short reaction times, high yields, and the remarkably low toxicity of bismuth compo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f15d916c6e200eaa723463eb2ef5682
https://doi.org/10.1002/chin.201541184
https://doi.org/10.1002/chin.201541184
Publikováno v:
Tetrahedron Letters. 54:983-985
The synthesis of dihydropyrimidinones and dihydropyrimidine thiones has attracted interest due to their biological activities. A common method for their synthesis is the Biginelli reaction, which is a one-pot condensation of an aryl aldehyde, urea (o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3136faf958b37008d25bed088cbd7d54
https://doi.org/10.1016/j.tetlet.2012.12.032
https://doi.org/10.1016/j.tetlet.2012.12.032
Publikováno v:
ChemInform. 44
The synthesis of dihydropyrimidinones and dihydropyrimidine thiones has attracted interest due to their biological activities. A common method for their synthesis is the Biginelli reaction, which is a one-pot condensation of an aryl aldehyde, urea (o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9b9ed5ed3cef9c5b51ceee27f2bf6b9
https://doi.org/10.1002/chin.201323150
https://doi.org/10.1002/chin.201323150
Autor:
Teresa M. Ferrell, Thomas J. Laughlin
Publikováno v:
Nature Biotechnology. 5:1035-1037
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b20064d64c50c1502d9a11073789efe
https://doi.org/10.1038/nbt1087-1035
https://doi.org/10.1038/nbt1087-1035
Autor:
Nathan Dean, William J. Herz, Thomas J. Laughlin, Daniel R. Coleman, Harold M. Draper, Chris NeSmith, K. Rajasekaran, C. Burns, I. K. Vasil, Clyde Kiker, Jonathan P. Gressel, Carolyn Fonyo, William G. Boggess, Clyde F. Kiker, R. L. Mott, S. J. Torreano, D. J. Frederick, Paul E. Barnett, H. G. Gibson, P. E. Pope, Chia M. Chen, J. Ken Pan, Gordon E. Monroe, Harold R. Sumner, S. C. Schank, Clinton J. Dawes, P. K. Chandra, F. A. Payne, Lalit R. Verma, John Goodrum, Peter H. Benson, K. K. Moorhead, D. A. Graetz, K. R. Reddy, P. A. Krottje, Mohammed K. Habbal, Richard P. Egg, Charlie G. Coble, Martin G. Tibbets, G. G. McBee, R. L. Monk, F. R. Miller, R. A. Nordstedt, D. D. Lee, T. L. Donaldson, Paul H. Smith, Hart Spiller, K. T. Shanmugam, Lars G. Ljungdahl, M. K. Hamdy, K. Kim, C. M. Ostrovski, J. C. Aitken, D. W. Tedder, R. C. Strickland, M. J. Beck, William L. Bryan, Irvin A. Jefcoat, Fawaz H. Jabali
Publikováno v:
Biomass Energy Development ISBN: 9781475705928
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0db164f19a3df11dfabe044cafadaf68
https://doi.org/10.1007/978-1-4757-0590-4_51
https://doi.org/10.1007/978-1-4757-0590-4_51
Conference
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Conference
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