Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Kapil, Upadhyaya"'
Publikováno v:
The Journal of Organic Chemistry. 88:3678-3696
Autor:
Brendan T. Freitas, Daniil A. Ahiadorme, Rahul S. Bagul, Ian A. Durie, Samir Ghosh, Jarvis Hill, Naomi E. Kramer, Jackelyn Murray, Brady M. O’Boyle, Emmanuel Onobun, Michael G. Pirrone, Justin D. Shepard, Suzanne Enos, Yagya P. Subedi, Kapil Upadhyaya, Ralph A. Tripp, Brian S. Cummings, David Crich, Scott D. Pegan
Publikováno v:
ACS Infectious Diseases. 8:596-611
Over the last 20 years, both severe acute respiratory syndrome coronavirus-1 and severe acute respiratory syndrome coronavirus-2 have transmitted from animal hosts to humans causing zoonotic outbreaks of severe disease. Both viruses originate from a
Publikováno v:
Angewandte Chemie. 133:25601-25607
Low-temperature NMR studies with a 4-C-methyl-4-O-benzoyl galactopyranosyl donor enable the observation and characterization of a bridged bicyclic dioxacarbenium ion arising from participation by a distal ester. Variable-temperature NMR studies revea
Publikováno v:
The Journal of Organic Chemistry. 86:12199-12225
The preparation of four per-O-benzyl-d- or l-glycero-d-galacto and d- or l-glycero-d-gluco heptopyranosyl sulfoxides and the influence of their side-chain conformations on reactivity and stereoselectivity in glycosylation reactions are described. The
Autor:
Christopher A. Rice, Scott D. Pegan, Joseph Media, Sandeep Dhanju, Kapil Upadhyaya, Frederick A. Valeriote, David Crich
Publikováno v:
Journal of the American Chemical Society. 142:9147-9151
We describe the synthesis of 10-aza-9-oxakalkitoxin, an N,N,O-trisubstituted hydroxylamine-based analog, or hydroxalog, of the cytotoxic marine natural product kalkitoxin in which the -NMe-O- moiety replaces a -CHMe-CH2- unit in the backbone of the n
Autor:
Kapil Upadhyaya, David Crich
Publikováno v:
Org Lett
We describe a formal synthesis of 10-aza-9-oxakalkitoxin, the hydroxalog of the cytotoxic marine natural product kalkitoxin, that features Mukaiyama Markovnikov silyl peroxidation of a terminal alkene and N-O bond formation as the central enabling st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::512de5ccd00b7426923949e3d9844ffe
https://europepmc.org/articles/PMC9004444/
https://europepmc.org/articles/PMC9004444/
Publikováno v:
J Org Chem
The preparation of four per-O-benzyl-d- or l-glycero-d-galacto and d- or l-glycero-d-gluco heptopyranosyl sulfoxides, and the influence of their side chain conformations on reactivity and stereoselectivity in glycosylation reactions are described. Th
Publikováno v:
Angew Chem Int Ed Engl
Low-temperature NMR studies with a 4-C-methyl-4-O-benzoyl galactopyranosyl donor enable the observation and characterization of a bridged bicyclic dioxacarbenium ion arising from participation by a distal ester. Variable temperature NMR studies revea
Autor:
Kapil Upadhyaya, Ravi Kumar Thakur, Gaurav Sharma, Kartikey Singh, Sanjeev K. Shukla, Prince Joshi, Renu Tripathi, Rama Pati Tripathi
Publikováno v:
European Journal of Medicinal Chemistry. 162:448-454
In an attempt to develop new antimalarial drugs, we have synthesized a new class of N-alkylated 3-glycoconjugated-oxopropylidene oxindoles starting from substituted isatins and glucopyranosyl propanone via a well-known cross-aldol reaction followed b
Autor:
Sandeep, Dhanju, Kapil, Upadhyaya, Christopher A, Rice, Scott D, Pegan, Joseph, Media, Frederick A, Valeriote, David, Crich
Publikováno v:
Journal of the American Chemical Society. 142(20)
We describe the synthesis of 10-aza-9-oxakalkitoxin, an