Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Phillip J. Fiore"'
Autor:
Jotham Wadsworth Coe, Phillip J. Fiore, Ian Edmonds, Jeffrey B. Sperry, Wiglesworth Kristin, Eugene Lvovich Piatnitski Chekler, Jonathan Langille, David C. Boyles, Roberta Louise Dorow, David B. Damon
Publikováno v:
Organic Process Research & Development. 18:1752-1758
This work describes the optimization and scale-up of a Buchwald–Hartwig amination reaction for the preparation of a pharmaceutical intermediate. This C–N bond formation is challenged by the use of a chiral primary amine, which both adds cost and
Publikováno v:
Organic Process Research & Development. 2:151-156
A manufacturing process to prepare two antiretroviral agents that denature the HIV-1 nucleocapsid protein (NCp7) has been developed and demonstrated on a pilot scale. 2,2‘-Dithiobis(benzoyl chloride) (4), prepared from commercially available 2,2‘
Publikováno v:
Organic Process Research & Development. 1:137-148
A manufacturing process to prepare the ACAT inhibitor 2,6-diisopropylphenyl [(2,4,6-triisopropylphenyl)acetyl]sulfamate (1; CI-1011) has been developed and successfully demonstrated on a pilot scale. Commercially available 1,3,5-triisopropylbenzene (
Publikováno v:
ChemInform. 28
Publikováno v:
ChemInform. 29
Autor:
Phillip J. Fiore, James G. Davidson
Publikováno v:
Nucleosides and Nucleotides. 10:1477-1483
A direct and efficient synthesis of 5′-deoxy-2′,3′-O-isopropylideneinosine, 7, from readily available inosine is described. An example of a potentially general synthesis of N -substituted-5′-deoxyadenosines from 7 is also described.