Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Narendra B. Ambhaikar"'
Autor:
Phil S. Baran, Narendra B. Ambhaikar, Carlos A. Guerrero, Benjamin D. Hafensteiner, David W. Lin, Jeremy M. Richter
Publikováno v:
ARKIVOC, Vol 2006, Iss 7, Pp 310-325 (2006)
Externí odkaz:
https://doaj.org/article/9e2831838cbd463dbe03794ff3458b47
Autor:
Narendra B. Ambhaikar
Publikováno v:
Current Drug Synthesis. :305-322
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::995cbe71281b8bd23849dd119917600f
https://doi.org/10.1002/9781119847281.ch16
https://doi.org/10.1002/9781119847281.ch16
Autor:
Anand M. Lahoti, Narendra B. Ambhaikar, D.M. Rajagopal Reddy, Arnab Roy, Kallam V.S.R. Krishna Reddy, S. Mahender Rao
Publikováno v:
Asian Journal of Chemistry. 34:1431-1438
Alcaftadine is an active pharmaceutical ingredient (API) used as an ophthalmic solution for the prevention of itching associated with allergic conjunctivitis. The originally reported synthesis uses a time-consuming column chromatography technique for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0dfc4c04e86e7ca4780b19301bec387
https://doi.org/10.14233/ajchem.2022.23672
https://doi.org/10.14233/ajchem.2022.23672
Publikováno v:
Progress in Heterocyclic Chemistry ISBN: 9780443189395
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04eae4814db5dae6da78c3a33e2c2d3b
https://doi.org/10.1016/b978-0-443-18939-5.00009-3
https://doi.org/10.1016/b978-0-443-18939-5.00009-3
Autor:
Narendra B. Ambhaikar, John D. Gallagher, Phil S. Baran, Carlos A. Guerrero, Benjamin D. Hafensteiner
Publikováno v:
Journal of the American Chemical Society. 128:8678-8693
In this article, full details regarding our total synthesis of avrainvillamide and the stephacidins are presented. After an introduction and summary of prior synthetic studies in this family of structurally complex anticancer natural products, the ev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3104680834feea155bdc19ae058a213e
https://doi.org/10.1021/ja061660s
https://doi.org/10.1021/ja061660s
Publikováno v:
Angewandte Chemie International Edition. 44:3892-3895
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f2088563bc80daf5b24c52c4a05b188
https://doi.org/10.1002/anie.200500655
https://doi.org/10.1002/anie.200500655
Autor:
Narendra B. Ambhaikar, Benjamin D. Hafensteiner, David W. Lin, Phil S. Baran, Jeremy M. Richter, Carlos A. Guerrero
Publikováno v:
ARKIVOC, Vol 2006, Iss 7, Pp 310-325 (2006)
There are remarkable advantages to be gained in terms of efficiency (lack of protecting groups, halogens, disposable functional groups), practicality (extremely concise sequences), stereocontrol (complete diastereoselectivity often observed), and con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9da4536fb7974bd9576c22c5b5bd3a13
https://doi.org/10.1002/chin.200723242
https://doi.org/10.1002/chin.200723242
Publikováno v:
Angewandte Chemie (International ed. in English). 44(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52e8914d30598209cbe22fe2b4a3be87
https://pubmed.ncbi.nlm.nih.gov/15586393
https://pubmed.ncbi.nlm.nih.gov/15586393
Publikováno v:
ChemInform. 34
We have discovered a novel and highly diastereoselective synthesis of azetinyl thiazolidine-2-thiones that utilizes additions of the chlorotitanium enolates of N-acyl thiazolidin-2-thiones to O-methyl aldoximes. The “anti” azetines can be subsequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cbbf42f6a0c89e06c877c3816c25bdf
https://doi.org/10.1002/chin.200332093
https://doi.org/10.1002/chin.200332093