Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Charles I. Grove"'
Autor:
Ruocheng Yu, Philipp Heretsch, Kyriacos C. Nicolaou, Verena Fetz, Charles I. Grove, Monette Aujay, Christopher R. H. Hale, Joseph Sandoval, Abdelatif ElMarrouni, Mark Brönstrup, Julia Gavrilyuk, Kiran Kumar Pulukuri, Stephan Rigol
Publikováno v:
Journal of the American Chemical Society. 138:6550-6560
A series of Δ(12)-prostaglandin J3 (Δ(12)-PGJ3) analogues and derivatives were synthesized employing an array of synthetic strategies developed specifically to render them readily available for biological investigations. The synthesized compounds w
Autor:
Philipp Heretsch, Kyriacos C. Nicolaou, Kiran Kumar Pulukuri, Stephan Rigol, Charles I. Grove, Christopher R. H. Hale, Abdelatif ElMarrouni, Ruocheng Yu
Publikováno v:
ChemInform. 47
The total synthesis of Δ(12) -prostaglandin J3 (Δ(12) -PGJ3 , 1), a reported leukemia stem cell ablator, through a number of strategies and tactics is described. The signature cross-conjugated dienone structural motif of 1 was forged by an aldol re
Autor:
Kyriacos C. Nicolaou, Philipp Heretsch, Abdelatif ElMarrouni, Kiran Kumar Pulukuri, Charles I. Grove, Ruocheng Yu, Stephan Rigol, Christopher R. H. Hale
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 22(25)
The total synthesis of Δ(12) -prostaglandin J3 (Δ(12) -PGJ3 , 1), a reported leukemia stem cell ablator, through a number of strategies and tactics is described. The signature cross-conjugated dienone structural motif of 1 was forged by an aldol re
Publikováno v:
Organic Letters. 14:4338-4341
Efficient and stereoselective syntheses of pigmentosin A, talaroderxine A, and its diastereomer talaroderxine B are reported. The binaphthyl ring system is assembled by vanadium-catalyzed phenolic coupling of tricyclic precursors. These key intermedi
Autor:
Sameer Urgaonkar, Young Sam Park, Marcos González-López, James C. Fettinger, Jared T. Shaw, Charles I. Grove
Publikováno v:
Angewandte Chemie International Edition. 50:3730-3733
The inhibition of bacterial cell division offers a new approach to controlling resistant bacterial infections.[1, 2] FtsZ is a protein of central importance to cell division that is often described as the prokaryotic homolog of tubulin because of the
Efficient and enantioselective syntheses of a family of 6,6′-binaphthopyranone natural products (viriditoxin, pigmentosin A, talaroderxine A, and talaroderxine B) are reported. A vanadium-catalyzed oxidative coupling provides the key axial chiralit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de1ad5a4b04cb3d697b618bd47da3e70
https://doi.org/10.1016/b978-0-12-417185-5.00010-7
https://doi.org/10.1016/b978-0-12-417185-5.00010-7
Autor:
Michelle B. Kim, Laura L. Lackner, Terrence E. O’Brien, David E. Anderson, Jared T. Shaw, Charles I. Grove, Jared T. Moore, Nohemy A. Sorto, James B. Ames
FtsZ is a guanosine triphosphatase (GTPase) that mediates cytokinesis in bacteria. FtsZ is homologous in structure to eukaryotic tubulin and polymerizes in a similar head-to-tail fashion. The study of tubulin's function in eukaryotic cells has benefi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::571af2593485dbfe36707b144cb4638a
https://europepmc.org/articles/PMC3514448/
https://europepmc.org/articles/PMC3514448/