Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Uko E. Udodong"'
Autor:
Michael E. Kopach, John L. Grutsch, Uko E. Udodong, Margaret M. Faul, Jeffrey Thomas Vicenzi, Michael A. Staszak, Christine A. Krumrich, Kevin A. Sullivan, Kobierski Michael Edward
Publikováno v:
Tetrahedron. 59:7215-7229
N-(Azacycloalkyl)bisindolylmaleimides 1 have been identified to be selective inhibitors of PKCβ. This manuscript will describe the synthetic approaches employed to prepare this class of compounds that resulted in development of efficient methods for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3754422089b9a9f7ff1ead1b08e2e36a
https://doi.org/10.1016/s0040-4020(03)00973-6
https://doi.org/10.1016/s0040-4020(03)00973-6
Autor:
William David Miller, John L. Grutsch, Uko E. Udodong, Harkness Allen Robert, Marvin M. Hansen, Verral Daniel Edward, Bret A. Astleford
Publikováno v:
Tetrahedron. 59:2667-2672
Echinocandin B (ECB) analog 1c was methylphosphonylated with the new reagent dimethyldiphosphonate 7 . Selective functionalization of the phenol group was achieved in the presence of 11 other reactive alcohol and amide groups. The phosphonylation was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8623bee745b30f8dddce073b9045eb1
https://doi.org/10.1016/s0040-4020(03)00310-7
https://doi.org/10.1016/s0040-4020(03)00310-7
Autor:
Carmichael Roberts, Uko E. Udodong, Robert Madsen, Bert Fraser-Reid, David R. Mootoo, Peter Konradsson
Publikováno v:
Journal of the American Chemical Society. 117:1554-1565
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4b2e5d3840e781946024e664ce5dc33
https://doi.org/10.1021/ja00110a011
https://doi.org/10.1021/ja00110a011
Publikováno v:
ChemInform. 22
N-Iodosuccinimide/trifluoromethanesulfonic acid, which had been shown to promote the solvolysis of disarmed n-pentenyl glycosides, has been found to induce the same reactivity with disarmed thioglycosides as substrates.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6865b811694a5c9e773a1a1561f5f5ac
https://doi.org/10.1002/chin.199133113
https://doi.org/10.1002/chin.199133113
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf59ac82d4efefd3184e616b426c3216
https://doi.org/10.1002/chin.199240247
https://doi.org/10.1002/chin.199240247
Autor:
J. R. Merritt, Zufan Wu, C. S. Rao, Uko E. Udodong, Håkan Ottosson, Carmichael S. Roberts, Bert Fraser-Reid, Robert Madsen
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87309b6ba31833a844e176ff6889aac0
https://doi.org/10.1002/chin.199342295
https://doi.org/10.1002/chin.199342295
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e525d7793c2dcdae0c1191ee4040395d
https://doi.org/10.1002/chin.199351259
https://doi.org/10.1002/chin.199351259
Autor:
Håkan Ottosson, C. Srinivas Rao, J. Robert Merritt, Uko E. Udodong, Bert Fraser-Reid, Robert Madsen, Zufan Wu, Carmichael Roberts
Publikováno v:
Synlett. 1992:927-942
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::666c6b55e764e2cfe2f50ffd17498800
https://doi.org/10.1055/s-1992-21543
https://doi.org/10.1055/s-1992-21543
Publikováno v:
Journal of the American Chemical Society. 113:5384-5392
(−)-Norsecurinine (2a) has been prepared in a stereospecific fashion with the acetylenic oxazole 39 as the starting material. Diels-Alder cyclization of 39 afforded the furano ketone 45 that was transformed in five steps to the butenolide mesylate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1efe8405232c388f41da53b01d528173
https://doi.org/10.1021/ja00014a033
https://doi.org/10.1021/ja00014a033
Publikováno v:
Tetrahedron Letters. 31:4313-4316
N-Iodosuccinimide/trifluoromethanesulfonic acid, which had been shown to promote the solvolysis of disarmed n-pentenyl glycosides, has been found to induce the same reactivity with disarmed thioglycosides as substrates.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2ce67036ff2de0da9f1894c9cc3f74c
https://doi.org/10.1016/s0040-4039(00)97609-3
https://doi.org/10.1016/s0040-4039(00)97609-3