Facile Synthesis of 4-H-Pyran Derivatives Bearing Indole Skeleton via[3+3]Cyclization of 3-Indolyl-3-oxopro-panenitriles with Dialkyl Acetylenedicarboxylates and Isocyanides

An efficient multicomponent reaction of 3-indolyl-3-oxopropanenitriles with dialkyl acetylenedicarboxylates and isocyanides under mild conditions leading to highly functionalized 6-(indol-3-yl)-4H-pyrans in moderate to good yields has been developed.

Three-component reaction of alkyl isocyanides with acetylenic esters and pyridine-2-carboxaldoxime or α-furildioxime:Synthesis and dynamic NMR study of ketenimines and bis(ketenimines)

The addition of pyridine-2-carboxaldoxime or α-furildioxime to dialkyl acety lenedicarboxy lates under neutral conditions in the presence of alkyl isocyanides leads to ketenimines and bis（ketenimines） in good yields.

A facile one-pot synthesis of functionalized thiazines in water

An efficient synthesis of thiazines from the three component reactions between dialkyl acetylenedicarboxylates, arylisothio- cyanates and N-nucleophiles at room temperature in water as the solvent is described.

Facile synthesis of N-(arylsulfonyl)-4-ethoxy-5-oxo-2,5-dihydro-1H-pyrolle-2,3-dicarboxylates by one-pot three-component reaction

Three-component reaction of arylsulfonamides,dialkyl acetylenedicarboxylates,and ethyl chlorooxoacetate promoted by triphenylphosphine and triethylamine provides a sufficient route for the synthesis of dialkyl N-（arylsulfonyl）-4-ethoxy-5-oxo-2,5-dihydro -1H-pyrolle-2,3-dicarboxylates in good yields.

Three-component synthesis and antibacterial evaluation of some novel 1,2-dihydroisoquinoline derivatives

Isoquinoline reacts with dialkyl acetylenedicarboxylates in the presence of kojic acid or8-hydroxyquinoline to generate 1,2-dihydroisoquinoline derivatives. The simplicity, mild reaction conditions and high yields of products make it an interesting process compared to other approaches. The compounds have been analyzed for antibacterial activity against Gram negative and Gram positive bacteria. The results indicated that 1,2-dihydroisoquinolines derived from kojic acid are effective against all of the studied bacteria especially against Bacillus subtilis, while the products obtained from8-hydroxyquinoline are active only against Gram positive bacteria.

An effcient synthesis of functionalized tetrahydro-1H-indeno[2,1-c]pyridine derivatives by a PPh_3-promoted condensation reaction between acetylene esters and 1,3-dioxo-N-aryl-2,3-dihydro-1H-indene-2-carboxamides

A reaction between 1,3-dioxo-N-aryl-2,3-dihydro-lH-indene-2-carboxamides, dialkyl acetylenedicar- boxylates, and triphenylphosphine or trimethylphosphite is described as a simple and efficient method for the synthesis of 5-hydroxy-4-aryl-2,5-dihydrofuran-2,3-dicarboxylate derivatives.

Efficient synthesis of functionalized butenolides mediated by vinyltriphenylphosphonium salts in aqueous media

An efficient synthesis of 5-oxo-2,5-dihydro-3-furancarboxylate derivatives via reaction of dialkyl acetylenedicarboxylate with triphenylphosphine （Ph3P） in the presence of activated carbonyl compounds such as ethyl pyruvate, benzil, benzoylcyanide, biacetyle or N-alkylisatins is described.

Facile, one-pot synthesis of new phenanthridine derivatives through 1,4-dipolar cycloaddition of phenantridine, activated acetylenes, and aromatic aldehydes

A facile, one-pot synthesis of new phenanthridine derivatives by a three-component reaction between phenantridine, dialkyl acetylenedicarboxylates（DAADs）, and aromatic aldehydes is described. The reaction is characterized by mild conditions, high selectivity, and tolerance to various functional groups.

Stereoselective Synthesis of Functionalized 1,3-Dienes in Water

An efficient synthesis of functionalized 1,3-dienes via one-pot reactions between dialkyl acetylenedicarboxylates, 1,3-dicarbonyl compounds and secondary amines in water as the solvent is described. The mild reaction condition high yields and the new products are advantages of our method.