Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Shankar Manyem"'
Autor:
Vladimir Bartus, Gregory R. Cook, Viera Lukacova, Xiaomin Jin, Mukund P. Sibi, Shankar Manyem, Sandeep R. Ghorpade, Yufen Zhang, Ethirajan Manivannan, Xiaoping Nie, Guorong Sun, Stefan Balaz
Publikováno v:
Chemical Biology & Drug Design. 72:237-248
Binding to the extracellular matrix, one of the most abundant human protein complexes, significantly affects drug disposition. Specifically, the interactions with extracellular matrix determine the free concentrations of small molecules acting in tis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55a4c7586b0e4d3b7bc2bf96aabeebd8
https://doi.org/10.1111/j.1747-0285.2008.00710.x
https://doi.org/10.1111/j.1747-0285.2008.00710.x
Publikováno v:
ARKIVOC, Vol 2006, Iss 4, Pp 189-199 (2006)
Scopus-Elsevier
Scopus-Elsevier
Treatment of an oxaziridine with low-valent iron or copper salts generates a carbon-centered radical able to cyclize onto an appended olefin.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c70ac0280fcd18fd378c5fb8ed8eaf07
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.0007.413
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.0007.413
Publikováno v:
Tetrahedron. 59:10575-10580
Radical additions to oxazolidinone acrylate followed by allyl trapping were studied with chiral Lewis acids derived from lanthanide salts. Chiral ligands were evaluated to establish the α-stereocenter. Ligands with a prolinol framework along with ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ce88556f262db2825e712c7c69d2646
https://doi.org/10.1016/j.tet.2003.07.019
https://doi.org/10.1016/j.tet.2003.07.019
Autor:
Mukund P. Sibi, Shankar Manyem
Publikováno v:
Tetrahedron. 56:8033-8061
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cea3d0a7d1be223cf90d8728e3d2403b
https://doi.org/10.1016/s0040-4020(00)00618-9
https://doi.org/10.1016/s0040-4020(00)00618-9
Autor:
Benjamin Neuenswander, Frank J. Schoenen, Jeffrey Aubé, Mukund P. Sibi, Shankar Manyem, Gerald H. Lushington
Publikováno v:
ChemInform. 38
A parallel synthesis of a library (80 members) of 2-pyrazolines in solution phase is described. The 2-pyrazoline core was accessed through the [3 + 2] cycloaddition of nitrilimines with enoyl oxazolidinones. The cycloaddition provided two regioisomer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9360b831fcdb3fa61f831da76d15e73
https://doi.org/10.1002/chin.200724110
https://doi.org/10.1002/chin.200724110
Publikováno v:
Journal of the American Chemical Society. 128(42)
The concept of "fluxional additives", additives that can adopt enantiomeric conformations depending on the chiral information in the ligand, is demonstrated in enantioselective Diels-Alder and nitrone cycloaddition reactions. The additive design is m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0425d9d944fd4f5cef2e0189880cd0a3
https://pubmed.ncbi.nlm.nih.gov/17044673
https://pubmed.ncbi.nlm.nih.gov/17044673
Publikováno v:
ChemInform. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e74b2ebb23a6db4f03c982b4b7b902b
https://doi.org/10.1002/chin.200446285
https://doi.org/10.1002/chin.200446285
Publikováno v:
ChemInform. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e52982edfd9a2f0ebb5542b2cfba1506
https://doi.org/10.1002/chin.200415109
https://doi.org/10.1002/chin.200415109
Publikováno v:
ChemInform. 34
In ligand design for asymmetric catalysis, the usual norm is to derive the face shielding elements from a chiral source. New ligands in which the face shielding is determined by fluxional groups are introduced. Their design, modular synthesis, and ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48113fc7bebc9de99783e77dd64c4586
https://doi.org/10.1002/chin.200346035
https://doi.org/10.1002/chin.200346035
Publikováno v:
Chemical reviews. 103(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::805c1846940fc098b76fe5e5793eb5a5
https://pubmed.ncbi.nlm.nih.gov/12914498
https://pubmed.ncbi.nlm.nih.gov/12914498