An efficient [4+ 3] annulation of 2-(1-tosylalkyl) phenols with C, N-cyclic azomethine imines
via in situ generation of ortho-quinone methides (o-QMs) under mild basic reaction …

A copper (II)-catalyzed cascade annulation of simple anilines with two molecules of alkyne
esters for the one-pot synthesis of 2, 4-disubstituted quinolines, with exclusive …

An efficient, secondary amine-catalyzed cascade annulation of 2-O/N-
propargylarylaldehydes with 2, 6-dialkylphenols was established to access biologically …

Abstract A diastereoselective [4+ 2] annulation reaction between in situ generated p‐
quinone methides and isatin‐derived enoates has been developed. In the presence of …

A powerful construction of 2-alkylquinolines and quinoline-2-carboxylates has been
successfully accomplished employing I2 and Mn (OAc) 3, respectively, to promote the …

A novel tandem intermolecular ammonium ylide formation/intramolecular Mannich-type [5+
1] cyclization reaction of aryl diazoacetates and ortho-aminophenyl imine derivatives was …

An effective annulation of ynones and (iso) quinoline N-oxides was developed to deliver
various functionalized 3-((iso) quinolin-1-yl)-4H-chromen-4-ones and 13H-isoquinolino [2, 1 …

We describe here an acid-mediated one-pot approach to access substituted xanthene and
thioxanthane derivatives from ortho-heteroaryl phenyl-substituted para-quinone methides …

The oxindole-embedded ortho-quinone methides were employed as reactive intermediates
in formal [4+ 2] annulation with 1, 3-dicarbonyls, providing an efficient access to spiro …

AP (NMe2) 3-catalyzed [4+ 2] annulation of 2-amino-β-nitrostyrenes and β′-acetoxy
allenoates followed by a Zn/AcOH-mediated reduction–hydroamination–isomerization has …