Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ronald J. Hinklin"'
Autor:
James T. Brewster, Samuel D. Randall, John Kowalski, Cole Cruz, Richard Shoemaker, Eugene Tarlton, Ronald J. Hinklin
Publikováno v:
Organic letters.
Photoredox-transition metal dual catalysis provides a unique platform for constructing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::623df0be9ed63f642cd28660b65f924c
https://pubmed.ncbi.nlm.nih.gov/36475829
https://pubmed.ncbi.nlm.nih.gov/36475829
Autor:
Jay B, Fell, John P, Fischer, Brian R, Baer, James F, Blake, Karyn, Bouhana, David M, Briere, Karin D, Brown, Laurence E, Burgess, Aaron C, Burns, Michael R, Burkard, Harrah, Chiang, Mark J, Chicarelli, Adam W, Cook, John J, Gaudino, Jill, Hallin, Lauren, Hanson, Dylan P, Hartley, Erik J, Hicken, Gary P, Hingorani, Ronald J, Hinklin, Macedonio J, Mejia, Peter, Olson, Jennifer N, Otten, Susan P, Rhodes, Martha E, Rodriguez, Pavel, Savechenkov, Darin J, Smith, Niranjan, Sudhakar, Francis X, Sullivan, Tony P, Tang, Guy P, Vigers, Lance, Wollenberg, James G, Christensen, Matthew A, Marx
Publikováno v:
Journal of medicinal chemistry. 63(13)
Capping off an era marred by drug development failures and punctuated by waning interest and presumed intractability toward direct targeting of KRAS, new technologies and strategies are aiding in the target's resurgence. As previously reported, the t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fc99717000ce420f505732f20b4224e4
https://pubmed.ncbi.nlm.nih.gov/32250617
https://pubmed.ncbi.nlm.nih.gov/32250617
Autor:
Ronald J. Hinklin, Laura L. Kiessling
Publikováno v:
ChemInform. 32
The advent of the Koenigs-Knorr method of glycosylation enabled the chemical synthesis of oligosaccharides.1 Since that advance, the differences in regiochemistry and stereochemistry of glycosyl linkages and variations in the stereoelectronic propert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e85c27f4b11a53126484ae52af549a99
https://doi.org/10.1002/chin.200130203
https://doi.org/10.1002/chin.200130203
Publikováno v:
ChemInform. 36
Stereoselective methods for the chemical synthesis of beta-N-glycosyl amides are needed to generate glycopeptides and glycoproteins. Here, we report that the Staudinger ligation can be used to form glycosylated asparagine derivatives. The reaction pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61a95fbfcabd4ed1a3a954bc07a34f43
https://doi.org/10.1002/chin.200513217
https://doi.org/10.1002/chin.200513217
Autor:
Laura L. Kiessling, Ronald J. Hinklin
Publikováno v:
Journal of the American Chemical Society. 123(14)
The advent of the Koenigs-Knorr method of glycosylation enabled the chemical synthesis of oligosaccharides.1 Since that advance, the differences in regiochemistry and stereochemistry of glycosyl linkages and variations in the stereoelectronic propert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb3e81655e0fb72c2dd4724d74c04adb
https://pubmed.ncbi.nlm.nih.gov/11457079
https://pubmed.ncbi.nlm.nih.gov/11457079