1465031-13-3Relevant academic research and scientific papers
A catalyst-free, efficient green MCR protocol for access to functionalized γ-carbolines in water
Dagar, Anuradha,Biswas, Soumen,Samanta, Sampak
, p. 52497 - 52507 (2015/06/25)
A general, mild, efficient and practical approach for the construction of functionalized γ-carboline derivatives has been successfully realized in water through a one-pot three-component reaction involving several aryl/hetero-aryl/alkyl/alkenyl/alkynyl/fe
L-Proline catalyzed stereoselective synthesis of (E)-methyl-α-indol- 2-yl-β-aryl/alkyl acrylates: Easy access to substituted carbazoles, γ-carbolines and prenostodione
Biswas, Soumen,Jaiswal, Pradeep Kumar,Singh, Shivendra,Mobin, Shaikh M.,Samanta, Sampak
supporting information, p. 7084 - 7087 (2013/10/22)
A simple, mild and robust method for the stereoselective synthesis of (E)-methyl α-(3-formyl-1H-indol-2-yl)-β-aryl/alkyl-substituted acrylates via a condensation reaction of methyl 2-(3-formyl-1H-indol-2-yl) acetate with several alkyl or aryl aldehydes using l-proline (25 mol%) as a catalyst is presented for the first time. In addition, completely metal free based high yielding methods for the syntheses of highly substituted biologically important carbazoles, γ-carbolines and the marine alkaloid prenostodione have been developed through our methodology.
