4945-38-4Relevant articles and documents
Enantioselective organocatalytic partial transfer hydrogenation of lactone-fused quinolines
Aillerie, Alexandre,Talance, Vincent Lemau De,Moncomble, Aurelien,Bousquet, Till,Pelinski, Lydie
supporting information, p. 2982 - 2985 (2014/06/23)
The first enantioselective synthesis of 4-aza-podophyllotoxin derivatives by partial transfer hydrogenation of lactone-fused quinolines was achieved using a chiral Bronsted acid catalyst. This reaction was extended to a large scope of substrates with good yields and enantioselectivities.
A NOVEL PHOTO-INDUCED SUBSTITUTION OF ALKYL 2-CYANO-3-QUINOLINECARBOXYLATES
Ono, Isao,Fujiki, Yoshiyuki,Fujinami, Naoki,Hoshi, Toshihiko
, p. 371 - 374 (2007/10/02)
Irradiation of 2-quinolinecarbonitriles having an alkoxycarbonyl group at the 3-position afforded five-membered and/or six-membered lactones in normal alcohols depending on their alkyl-chain-length, whereas the irradiation in 2-propanol and t-butyl alcohol did not cause any cyclization, but instead decyanated and methylated products were obtained, respectively.
A new method for the preparation of 2 hydroxymethyl 3 quinoline carboxylic acid lactone derivatives
Kurihara,Michida,Hirano
, p. 2451 - 2453 (2007/10/04)
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