Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Karthik S. Iyer"'
Publikováno v:
JACS Au, Vol 4, Iss 2, Pp 680-689 (2024)
Externí odkaz:
https://doaj.org/article/95ff415ee5714db1a6fd1de5f23529de
Autor:
Joseph R. A. Kincaid, Juan C. Caravez, Karthik S. Iyer, Rahul D. Kavthe, Nico Fleck, Donald H. Aue, Bruce H. Lipshutz
Publikováno v:
Communications Chemistry, Vol 5, Iss 1, Pp 1-7 (2022)
The antiviral drug nirmatrelvir is the active ingredient in Paxlovid, a SARS-CoV-2 Mpro inhibitor developed by Pfizer, however, its synthetic procedure faces limitations for meeting urgent demand. Here, the authors optimize the key synthetic steps an
Externí odkaz:
https://doaj.org/article/c6511b695b1d4b759ca58f72f163042a
Publikováno v:
Green Chemistry. 25:2663-2671
Facile reductions of carboxylic acids to aldehydes or alcohols can be effected under mild conditions upon initial conversion to their corresponding S-2-pyridyl thioesters.
Publikováno v:
Organic Letters. 24:9049-9053
Publikováno v:
Green Chemistry. 24:3640-3643
A green sequence to lapatinib has been developed as a representative example showcasing the technologies that are available today for applications to targets in the fine chemicals industry.
Publikováno v:
Chemical science, vol 14, iss 23
A 6-step synthesis of the antimalarial drug candidate MMV688533 is reported. Key transformations carried out under aqueous micellar conditions include two Sonogashira couplings and amide bond formation. Compared with the first-generation manufacturin
Autor:
Bruce H. Lipshutz, Xiaohan Li, David K. Leahy, Ruchita R. Thakore, Karthik S. Iyer, J. Daniel Bailey
Publikováno v:
Organic Letters. 23:7205-7208
Highly valued products resulting from reductive aminations utilizing shelf-stable bisulfite addition compounds of aldehydes can be made under aqueous micellar catalysis conditions. Readily available α-picolineborane serves as the stoichiometric hydr
Autor:
Joseph R. A. Kincaid, Juan C. Caravez, Karthik S. Iyer, Rahul D. Kavthe, Nico Fleck, Bruce H. Lipshutz
A convergent route to the antiviral drug nirmatrelvir is described, arriving at the targeted drug in 45% overall yield with no loss of stereointegrity. Critical amide bond-forming steps utilize green technology that avoids traditional peptide couplin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::586581a82afe35d4d8cb715289d825ac
https://doi.org/10.26434/chemrxiv-2022-hmdd4
https://doi.org/10.26434/chemrxiv-2022-hmdd4
Publikováno v:
Current Opinion in Green and Sustainable Chemistry. 38:100686
Publikováno v:
Current Opinion in Green and Sustainable Chemistry. 31:100493
Reactions are discussed that lead to the valuable amine functional group in aromatics and heteroaromatics, carried out under sustainable conditions in water enabled by micellar catalysis. These new technologies are general and have been successfully