115363-86-5Relevant academic research and scientific papers
Design and optimization of tricyclic phtalimide analogues as novel inhibitors of HIV-1 integrase
Verschueren, Wim G.,Dierynck, Inge,Amssoms, Katie I. E.,Hu, Lili,Boonants, Paul M. J. G.,Pille, Geert M. E.,Daeyaert, Frits F. D.,Hertogs, Kurt,Surleraux, Dominique L. N. G.,Wigerinck, Piet B. T. P.
, p. 1930 - 1940 (2007/10/03)
Human immunodeficiency virus type-1 integrase is an essential enzyme for effective viral replication and hence a valid target for the design of inhibitors. We report here on the design and synthesis of a novel series of phthalimide analogues as integrase
Formation of Fused Tricyclic Azetidinones and Pyrrolidinones by Intramolecular SH2 Processes
Beckwith, A. L. J.,Boate, D. R.
, p. 4339 - 4348 (2007/10/02)
Treatment of a variety of suitably substituted sulfides of N-(o-halobenzyl)- or N-(o-halophenyl)azetidinone (e.g., 4 and 8) and -pyrrolidinone (e.g., 12 and 14) systems with either tributylstannane or tributyltin deuteride affords, by aryl radical substit
