90359-73-2Relevant academic research and scientific papers
Hepatitis C virus inhibitors
-
Page/Page column 586, (2017/01/23)
Hepatitis C virus inhibitors having the general formula (I) are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.
Hepatitis C Virus Inhibitors
-
Page/Page column, (2013/05/21)
Hepatitis C virus inhibitors having the general formula (I) are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.
Synthesis of 7-(4-piperidyl)- [1,6]naphthyridin-5-one and 3-(4-piperidyl)isoqunolin-1-one
Kovalskiy,Perevalov
experimental part, p. 1503 - 1507 (2010/07/04)
7-(4-Piperidyl)[1,6]napththiridin-5-one was synthesized on the basis of 2-methylnicotinic acid. 3-(4-Piperidyl)isoquinolin-1-one was synthesized from the diethylamide of o-toluic acid and Weinreb′s amide of N-Boc-isonipecotic acid.
Hepatitis C Virus Inhibitors
-
Page/Page column 79, (2008/12/05)
Hepatitis C virus inhibitors having the general formula are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.
HEPATITIS C VIRUS INHIBITORS
-
Page 136-137, (2008/06/13)
Hepatitis C virus inhibitors are disclosed having the general formula:(I) wherein R1, R2, R3, R', B, Y and X are described in the description. Compositions comprising the compounds and methods for using the compounds toinhibit HCV are also disclosed.
Directed Metalation of N,N-Diethylbenzamides. Silylated Benzamides for the Synthesis of Naturally Occurring pero-Methylanthraquinones and peri-Methyl Polycyclic Aromatic Hydrocarbons
Mills, Robert J.,Snieckus, Victor
, p. 4386 - 4390 (2007/10/02)
Efficient methodologies based on directed ortho metalation, fluoride-induced carbodesilylation, and metal-halogen exchange processes (Scheme I) are reported for the synthesis of peri-methyl-substituted anthraquinone natural products 5 and polycyclic aroma
SILICON IN BENZAMIDE DIRECTED ORTHO METALATION REACTIONS SYNTHESIS OF PERI-METHYL SUBSTITUTED PAHs AND NATURAL ANTHRAQUINONES
Mills, R.J.,Snieckus, V.
, p. 479 - 482 (2007/10/02)
The α,α-bis(trimethylsilyl)-o-toluamides 4 and 9, systems protected from benzylic deprotonation, are available starting materials for the short syntheses of peri-methyl substituted benz(a)anthraquinones 6a and 6b and desoxyerythrolaccin trimethyl ether 12 respectively.
