Gary H. Birnberg
Pearl River Community College(US)
Publications by Year
Research Areas
Chemical Reaction Mechanisms, Synthesis and biological activity, Coordination Chemistry and Organometallics, Phenothiazines and Benzothiazines Synthesis and Activities, Chemical Synthesis and Reactions
Most-Cited Works
- → Discovery of 4-(Benzylaminomethylene)isoquinoline-1,3-(2H,4H)-diones and 4-[(Pyridylmethyl)aminomethylene]isoquinoline-1,3-(2H,4H)-diones as Potent and Selective Inhibitors of the Cyclin-Dependent Kinase 4(2009)73 cited
- → 4-(Phenylaminomethylene)isoquinoline-1,3(2H,4H)-diones as Potent and Selective Inhibitors of the Cyclin-Dependent Kinase 4 (CDK4)(2008)63 cited
- → Cheletropic .sigma.2s + .sigma.2s + .sigma.2s ejection of nitrogen from 9,10-diazasnoutenes as a route to monofunctionalized semibullvalenes. Ground state substituent effects on equilibrium displacements(1974)50 cited
- → Synthesis and Biological Activity of Analogues of the Antimicrotubule AgentN,β,β-Trimethyl-l-phenylalanyl-N-[(1S,2E)-3-carboxy-1-isopropylbut-2-enyl]-N1,3-dimethyl-l-valinamide (HTI-286)(2004)49 cited
- → Discovery and optimization of 2-(4-substituted-pyrrolo[2,3-b]pyridin-3-yl)methylene-4-hydroxybenzofuran-3(2H)-ones as potent and selective ATP-competitive inhibitors of the mammalian target of rapamycin (mTOR)(2010)39 cited
- → Silver(1+) ion-catalyzed rearrangements. XXIV. Direct and indirect trapping of isomeric monosubstituted bicyclo[4.2.0]octadienes with triazolinediones. Photocyclization and silver(1+) ion-catalyzed rearrangement of the derived adducts as a route to functionalized 9,10-diazasnoutanes(1974)29 cited
- → 4-Substituted-7-azaindoles bearing a ureidobenzofuranone moiety as potent and selective, ATP-competitive inhibitors of the mammalian target of rapamycin (mTOR)(2010)20 cited
- → D-piece modifications of the hemiasterlin analog HTI-286 produce potent tubulin inhibitors(2004)20 cited
- → 4-Anilino-7,8-dialkoxybenzo[g]quinoline-3-carbonitriles as Potent Src Kinase Inhibitors(2005)16 cited
- → Stereoselective 1,4 bromination of semibullvalene and tri-n-butyltin hydride reduction of the dibromide(1973)13 cited