Drupal-Biblio17<style face="normal" font="default" size="100%"> Accessing alpha-arylated nitriles via BF3 center dot OEt2 catalyzed cyanation of para-quinone methides using tert-butyl isocyanide as a cyanide source</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Identification of potent chromone embedded [1,2,3]-triazoles as novel anti-tubercular agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Transition metal free regio-selective C–H hydroxylation of chromanones towards the synthesis of hydroxyl-chromanones using PhI(OAc)2 as the oxidant</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Alternative synthesis of the CNS stimulant Prolintane</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient and cost effective synthesis of acetamides catalyzed by calcium chloride</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient synthesis of optically active neolignans ligraminol D and E</style>Drupal-Biblio17<style face="normal" font="default" size="100%">New enantioselective synthesis of antiobesity drug lorcaserin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Oxone promoted dehydrogenative Povarov cyclization of N-aryl glycine derivatives: an approach towards quinoline fused lactones and lactams</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis, biological evaluation and molecular modeling studies of novel chromone/Aza-chromone fused α-aminophosphonates as Src kinase inhibitors</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis, biological evaluation and molecular modeling studies of novel chromone/Aza-Chromone fused alpha-aminophosphonates as src kinase inhibitors</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of marine natural products serinolamide A and columbamide D</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Transition-metal-free benzannulation of tricarbonyl derivatives with arynes: access to 1,3-dinaphthol precursors for the synthesis of rhodamine dye analogues</style>Drupal-Biblio17<style face="normal" font="default" size="100%">1,6-Conjugate addition initiated formal [4+2] annulation of p-quinone methides with sulfonyl allenols: a unique access to spiro[5.5]undeca-1,4-dien-3-one scaffolds</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Silver-catalyzed cascade cyclization/1,6-conjugate addition of homopropargyl sulfonamides to p-quinone methides: an approach to diverse 3-diarylmethine substituted dihydropyrroles</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Iron catalyzed tandem ring opening/1,6-conjugate addition of cyclopropanols with p-quinone methides: new access to gamma,gamma-diaryl ketones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Metal- and light-free direct C-3 ketoalkylation of quinoxalin-2(1H)-ones with cyclopropanols in aqueous medium</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Metal-free aminocarbonylation of p-quinone methides with isocyanides: synthesis of sterically hindered alpha-arylated acetamides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Thallium(III) p-tosylate (TTS) mediated oxidative rearrangement of 2-naphthyl and 2-heteroarylchromanones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">BF3.Et2O-catalyzed selective C-4 alkylation of isoquinolin1(2H)-ones employing p-quinone methides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Metal- and photocatalyst-free, visible-light-initiated C3 a-aminomethylation of quinoxalin-2(1H)-ones via electron donor-acceptor complexes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Palladium-catalyzed oxidative cyclization of ?-allenols in the presence of TBN: access to 3(2H)-furanones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Cu-catalyzed multicomponent reaction of arylhydrazines with β-ketoesters and TBN: one-pot access to N 2-aryl 1,2,3-triazole-1-oxides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Visible-light mediated C-3 amination of quinoxalin-2(1H)-ones via electron donor-acceptor complexation</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Ag(I)-catalyzed heterocyclization/[3+2] cycloaddition of α-alkynylenones with β-enaminones: tandem access to highly substituted cyclopenta[c]furans</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient Copper-Catalyzed, One-Pot Synthesis of N2-Aryl Phosphoryl 1,2,3-Triazole 1-Oxides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Iron mediated oxidative ring opening-homocoupling of cyclopropanols: facile access to 1,6-diketones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Manganese-mediated cascade radical oxidative cyclization/1,6-conjugate addition of unsaturated oximes with p-quinone methides: facile access to β,β-diarylmethine substituted isoxazolines</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Phosphine-catalyzed nucleophilic ring opening of cyclopropenones with sulfoximines to access N-α,β-unsaturated acyl sulfoximines</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Copper-catalyzed radical 1,2-oxysulfoximination of β,γ-unsaturated oximes for the synthesis of sulfoximine-substituted isoxazolines</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Radical-promoted cyclization of 3-allyl-2-arylquinazolinones mediated by silver(i) salts to access SCF3/SCN-enriched dihydroisoquinolino[1,2-b]quinazolinones</style>