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.
萘醌的串联合成是由
漆酶生成的醌和无环二烯通过Diels-Alder反应进行的。该反应在温和的条件下在
水性介质中进行,得到高达80%的
萘醌。另外,还研究了溶剂的作用,并且表明
水对于该反应是最佳的。