Laccase-generated quinones in naphthoquinone synthesis via Diels–Alder reaction
S Witayakran, A Zettili, AJ Ragauskas
Index: Witayakran, Suteera; Zettili, Abdullah; Ragauskas, Arthur J. Tetrahedron Letters, 2007 , vol. 48, # 17 p. 2983 - 2987
Full Text: HTML
Citation Number: 42
Abstract
The tandem synthesis of naphthoquinones was conducted from the reaction of laccase- generated quinones and acyclic dienes via Diels–Alder reaction. This reaction was carried out under mild condition in aqueous medium and yielded naphthoquinones up to 80%. In addition, the effect of solvent was also investigated and water was shown to be optimal for this reaction.
Related Articles:
[Yamaguchi, Satoru; Shinoda, Hiroyuki; Inoue, Masami; Enomoto, Saburo Chemical and Pharmaceutical Bulletin, 1986 , vol. 34, # 11 p. 4467 - 4473]
[Uyanik, Muhammet; Mutsuga, Tatsuya; Ishihara, Kazuaki Molecules, 2012 , vol. 17, # 7 p. 8604 - 8616]
[Bansal, Vandana; Sharma, Jyotsana; Khanna, Rajinder N. Journal of Chemical Research - Part S, 1998 , # 11 p. 720 - 721]
[Henrion, Jean-Christophe; Jacquet, Bernard; Hocquaux, Michel; Lion, Claude Bulletin des Societes Chimiques Belges, 1994 , vol. 103, # 4 p. 163 - 168]
[Citterio, Attilio; Santi, Roberto; Fiorani, Tiziana; Strologo, Sauro Journal of Organic Chemistry, 1989 , vol. 54, # 11 p. 2703 - 2712]