Double michael addition reactions to tetrakis sulfonyl activated olefins

A new class of bis Michael adducts are prepared from 1,3‐bis‐[2‐(2‐arylethenesulfonyl)‐vinyl]‐benzenes and 1,4‐bis‐[2‐(2‐arylethenesulfonyl)‐vinyl]‐benzenes by double Michael addition reaction with active methylene compounds.     

2,6‐Diaryl‐4,4‐disubstituted‐4H‐thiopyran: Source for spiro heterocycles

The 1,5‐diaryl‐3,3‐disubstituted‐1,5‐pentanedione on reaction with ammonium acetate, phosphorus pentoxide and phosphorus pentasulfide gave respective 1,4‐dihydropyridine, 4H‐pyran and 4H‐thiopyran. Novel spiro heterocycles have been obtained by the cyclocondensation of 4H‐thiopyran with hydrazine, hydroxylamine, urea and thiourea.     

Gem‐disubstituted 4‐oxocyclohexanes: Source for spiro heterocycles

Novel spiro heterocycles, substituted spiro‐pyrimidine, pyrazole and isoxazole compounds are prepared by the cyclocondensation of 4‐oxocyclohexane gem‐dicarboxylates and cyano esters with nucleophiles.     

Synthesis and Antimicrobial Activity of a New Class of Sulfonylmethane Linked Bisheterocycles

A new class of sulfonylmethane linked bisheterocycles were prepared and studied their antimicrobial activity.     

Synthesis of Amido‐linked Oxazolyl/Thiazolyl/Imidazolyl Pyrazoles and Isoxazoles

The amido‐linked oxazolyl/thiazolyl/imidazolyl pyrazoles and isoxazoles were prepared from the synthetic intermediates oxazolyl/thiazolyl/imidazolyl acrylamides adpoting1,3‐dipolar cycloaddition of nitrile imines and nitrile oxides.     

2‐Arylethenyl‐2′‐arylethynyl sulfones: A potential source for some spiroheterocycles

The double Michael addition of dimethyl malonate to 2‐arylethenyl‐2′‐arylethynyl sulfones (3) resulted in 3,5‐diaryl‐5,6‐dihydro‐4,4‐dimethoxycarbonyl‐1‐thiin‐1,1‐dioxides (4) . The latter on cyclocondensation with urea / thiourea / hydrazine hydrate / hydroxylamine hydrochloride gave spiroheterocycles.     

Structure determination of N‐methyl‐tetrahydro‐5H‐indazol‐5‐ones

This paper communicates the (regio) synthesis and a convenient NMR structural assignment method for N‐methyl‐tetrahydro‐5H‐indazol‐5‐one isomers. The cyclization reaction of 7‐(hydroxymethylene)‐1,4‐dioxaspiro[4,5]decan‐8‐one ( 3 ) with methylhydrazine yields, after de‐protection predominately the N‐2 methyl isomer 2 . Analysis of the product ratio and structural assignments are based on NMR data including NOE difference experiments and subsequently confirmed with X‐ray crystallography. These findings are in sharp contrast with the literature. The experimental conditions used to optimize the synthesis of the individual isomers are discussed.