Cyclic secondary amines and 2-hydroxybenzaldehydes or related ketones react to furnish
benzo [e][1, 3] oxazine structures in generally good yields. This overall redox-neutral amine …

The 1, 3-dipolar cycloaddition of azomethine ylides derived from substituted isatins and 1, 3-
thiazolane-4-carboxylic acid to a series of 2-(arylmethylene)-2, 3-dihydro-1H-inden-1-ones …

Spirooxindolo-pyrrolidine, pyrrolizine and pyrrolothiazole hybrid compounds were obtained
in excellent yields from the regio-and stereoselective reaction between β-nitrostyrenes and …

A facile 1, 3-dipolar cycloaddition of azomethine ylide generated in situ from the reaction of
1, 3-thiazolane-4-carboxylic acid and isatin to 2-arylidene-1, 3-indanediones furnished …

Ionic liquid (IL) catalysed organic syntheses have emerged as a great approach to improve
synthetic productivity. Particularly IL catalyzed domino reactions enable the synthesis of …

We have performed a combined computational and experimental study to elucidate the
mechanism of a metal-free α-amination of secondary amines. Calculations predicted …

Redox Isomerization via Azomethine Ylide Intermediates: N-Alkyl Indoles from Indolines and
Aldehydes | Organic Letters ACS ACS Publications C&EN CAS Find my institution Log In …

A series of novel 2-aryl-3, 4-dihydro-2H-thieno [3, 2-b] indoles has been synthesised
regioselectively in good yields from the reaction of 5-aryldihydro-3 (2H)-thiophenones and …

Secondary amines undergo redox-neutral reactions with aminobenzaldehydes under
conventional and microwave heating to furnish polycyclic aminals via amine α-amination/N …

The domino reactions of pyridine/isoquinoline, bromoacetonitrile/ethyl bromoacetate and a
series of β-nitrostyrenes in the presence of triethylamine afforded novel tri-/disubstituted …