Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Charles S. Shanahan"'
Autor:
Charles S. Shanahan, Appasaheb L. Kadam, Barreddi Chiranjeevi, Aline A. Nunes, Aravindan Jayaraman, Saeed Ahmad, Sarah L. Aleshire, Kai O. Donsbach, B. Frank Gupton, Michel C. Nuckols
Nirmatrelvir, the novel antiviral component of Pfizer’s orally available combination therapy Paxlovid, used to treat COVID-19, presents a significant synthetic challenge. Herein, we report process optimization insights that could enable a scalable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2a3122a9a6b3664e212d2ce214e878a
https://doi.org/10.26434/chemrxiv-2022-cn0k1
https://doi.org/10.26434/chemrxiv-2022-cn0k1
Publikováno v:
SAE International Journal of Fuels and Lubricants. 10
Publikováno v:
Tetrahedron. 69:7592-7607
A formal synthesis of didehydrostemofoline and isodidehydrostemofoline has been accomplished by preparing an intermediate in the Overman synthesis of these alkaloids from commercially available 2-deoxy- d -ribose. The work presented in this account c
Publikováno v:
European Journal of Organic Chemistry. 2013:6032-6037
A Lewis acid mediated coupling reaction of enol-diazo nucleophiles and propargyl acetates has provided rapid and diverse access to complex alkynyl-tethered diazocarbonyl compounds. The ability of the coupling reaction to vary critical functionality f
Publikováno v:
Angewandte Chemie International Edition. 51:10596-10599
Sweet to the Core Enantioselective formal total syntheses of the Stemona alkaloids didehydrostemofoline and isodidehydrostemofoline were accomplished in 24 steps from commercially available 2-deoxy-d-ribose. The synthesis features a novel cascade of
Publikováno v:
Organic Letters. 14:3608-3611
The intramolecular acid catalyzed aldol cyclization of 2,3,7-triketoesters formed from ζ-keto-α-diazo-β-ketoesters provides highly functionalized cyclopentanones with good diastereoselectivity in high overall yields via kinetically controlled and
Publikováno v:
New J. Chem.. 36:492-505
Linear analogs have been synthesized to model disassembling dendrimers. These linear analogs provide a facile synthesis to molecules that can be used to test new trigger groups and cleavage vectors. Vanillin and o-vanillin were used as the monomer un
Publikováno v:
Tetrahedron Letters. 52:4076-4079
Novel, intramolecular 1,3-dipolar cycloadditions of azomethine ylides have been applied to the synthesis of functionalized core structures of the stemofoline alkaloids. In an effort to maximize the efficiency of this key transformation in the context
Publikováno v:
Organic Letters. 12:4944-4947
The convergent synthesis of geometrically degradable dendrimers based on the 2,4-bis(hydroxymethyl)phenol subunit is presented. The key step of the synthetic scheme involves the CuI/3,4,7,8-tetramethyl-1,10-phenanthroline-catalyzed coupling of aryl i
Publikováno v:
ChemInform. 46
Recent studies of diastereoselective conjugate additions of monoorganocuprates, Li[RCuI], to chiral γ-alkoxycrotonates and fumarates are disclosed. This methodology was applied to the shortest total synthesis of (-)-dihydroprotolichesterinic acid to