930-63-2Relevant academic research and scientific papers
Non-Nucleoside reverse transcriptase inhibitors
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Page/Page column 15, (2009/01/23)
Compounds of formula I, wherein R1, R2, R3, X and Ar, are as defined herein or pharmaceutically acceptable salts thereof, inhibit HIV-1 reverse transcriptase and afford a method for prevention and treatment of HIV-1 infections and the treatment of AIDS and/or ARC. The present invention also relates to compositions containing compounds of formula I useful for the prevention and treatment of HIV-1 infections and the treatment of AIDS and/or ARC.
DISILYLATED COMPOUNDS AS PRECURSORS OF HETEROCYCLES: SYNTHESIS OF BENZIMIDAZOLES, TRIAZOLES, FURAN AND PYRROLE.
Rigo, Benoit,Valligny, Dominique,Taisne, Sophie
, p. 167 - 180 (2007/10/02)
The cyclization of disilylated compounds catalyzed by trifluoromethanesulfonoc acid is an easy way to obtain some heterocycles such as benzimidazole, triazole, furan and pyrrole.
ACETALS OF LACTAMS AND ACID AMIDES. 37. * REACTIONS OF AMIDE AND LACTAM ACETALS WITH DERIVATIVES OF UREA AND URETHANE AND SYNTHESIS OF CONDENSED PYRIMIDINES
Kaimanakova, S. I.,Kuleshova, E. F.,Solov'eva, N. P.,Granik, V. G.
, p. 1208 - 1211 (2007/10/02)
The reactions of diethylacetals of dimethylacetamide and N-methylbutyro-, -valero-, and -caprolactams with urea, thiourea, and urethane lead to the corresponding N-carbamide- and N-ethoxycarbonylamides, on the basis of which derivatives of pyrimidine and pyrrolo- and pyridopyrimidine and pyridoazepine, as well as triazole derivatives, were synthetized.
