a convenient and efficient procedure for the synthesis of 14-aryl or alkyl-14h-dibenzo[a,j]xanthenes by condensation of 2-naphthol and aldehydes in the presence of methylimidazolium hydrogensulfate, as a brönsted acidic ionic liquid ([hmim]hso4), is described. both aromatic and aliphatic aldehydes reactedeasily to afford the corresponding 14-aryl or alkyl-14h-dibenzo[a,j]xanthenes in good yield...

Secondary benzylic alcohols and diarylmethanols are common structural motifs of biologically active medicinally relevant compounds. Here we report their enantioselective synthesis by ?-arylation primary aliphatic under sequential catalysis integrating a Ru-catalyzed hydrogen transfer oxidation nucleophilic addition. The method can be applied to various aryl nucleophiles tolerating range functio...

The development of methodologies for C-N bond formation reactions is an important scientific challenge because of many academic and industrial applications. This work will focus particularly on palladium-catalyzed cross-couplings of amine-containing compounds with aryl halides. The scope of the BrettPhos precatalyst for the cross-coupling of ortho-substituted aryl iodides with amides is studied...

A convenient and efficient procedure for the synthesis of 14-aryl or alkyl-14H-dibenzo[a,j]xanthenes by condensation of 2-naphthol and aldehydes in the presence of Methylimidazolium hydrogensulfate, as a Brönsted acidic ionic liquid ([Hmim]HSO4), is described. Both aromatic and aliphatic aldehydes reacted easily to afford the corresponding 14-aryl or alkyl-14H-dibenzo[a,j]xanthenes in good yiel...

A convenient and efficient procedure for the synthesis of 14-aryl or alkyl-14H-dibenzo[a,j]xanthenes by condensation of 2-naphthol and aldehydes in the presence of Methylimidazolium hydrogensulfate, as a Brönsted acidic ionic liquid ([Hmim]HSO4), is described. Both aromatic and aliphatic aldehydes reacted easily to afford the corresponding 14-aryl or alkyl-14H-dibenzo[a,j]xanthenes in good yiel...

Benzoyl azides were used for the direct and atom economic C–H amidation of electron rich heteroarenes in the presence of phosphoric acid, a photocatalyst and visible light. Hetero-aromatic amides are obtained in good yields at very mild reaction conditions with dinitrogen as the only by-product. The reaction allows the use of aryl-, heteroarylor alkenyl acyl azides and has a wide scope for hete...

Benzoyl azides were used for the direct and atom economic C-H amidation of electron rich heteroarenes in the presence of phosphoric acid, a photocatalyst and visible light. Hetero-aromatic amides are obtained in good yields at very mild reaction conditions with dinitrogen as the only by-product. The reaction allows the use of aryl-, heteroaryl- or alkenyl acyl azides and has a wide scope for he...

Abstract In this article we report that a cationic version of Akiba's Bi III complex catalyzes the reduction amides to amines using silane as hydride donor. The catalytic system features low catalyst loadings and mild conditions, en route secondary tertiary aryl‐ alkylamines. tolerates functional groups such alkene, ester, nitrile, furan thiophene. Kinetic studies on reaction mechanism result i...

A convenient, efficient and practical procedure for the synthesis of 1-amidoalkyl 2-naphthols is described by condensation of aromatic aldehydes with amides and 2-naphthol in the presence of P2O5/SiO2 as an efficient catalyst. Moreover, in the present of this catalyst, the synthesis of 14-aryl or alkyl-14H-dibenzo[a,j]xanthenes is studied by co...