1609076-76-7Relevant academic research and scientific papers
Regioselective synthesis of 3,4,6,7-tetrahydro-3,3-dimethyl-9-phenyl-2H-xanthene-1,8(5H,9H)-diones through ascorbic acid catalyzed three-component domino reaction
Napoleon, Ayyakannu Arumugam,Khan, Fazlur-Rahman Nawaz,Jeong, Euh Duck,Chung, Eun Hyuk
, p. 5656 - 5659 (2014)
An efficient, three-component domino reaction of dimedone 1, aromatic aldehydes (2a-o), and 1,3-cyclohexanedione 1a in the regio-selective synthesis of 3,3-dimethyl-9-phenyl-2H-xanthene-1,8(5H,9H)-diones (3a-o) is reported. The desired product, 3 is effic
Three-component reactions of aromatic aldehydes and two different nucleophiles and their leaving ability-determined downstream conversions of the products
Li, Minghao,Taheri, Amir,Liu, Meng,Sun, Shaohuan,Gu, Yanlong
, p. 537 - 556 (2014/05/20)
Many three-component reactions of aromatic aldehydes with activated methylene derivatives and an associated nucleophile have been developed by using l-proline as the catalyst. Nucleophiles, such as indoles, thiophenols, mercaptans, 2-methylfuran and benze
