会议专题

SYNTHESIS OF NATURAL PRODUCTS BEARING BENZOPYRANS MOIETY BY A DOMINO REACTIONS

An simple and general synthesis of benzopyrans was achieved by ethylenediamine diacetate-catalyzed reactions of resorcinols with a, p-unsaturated aldehydes in moderate yields by domino reactions. Also, an efficient and concise synthetic route for polycycles bearing citran, cyclol, and chalcone nuclei was developed starting from a variety of trihydroxybenzenes with substituents on the ring. These two methodologies were applied successfully to the synthesis of a number of biologically interesting natural products bearing benzopyrans.

benzopyrans polycycles domino reactions natural products.

Wang Xue Xia Likai Li Xin Yong Rok Lee

School of Chemical Engineering and Technology, Yeungnam University, Gyeongsan 712-749, Republic of Korea

国际会议

The 7th International Forum on Post-Genome Technologies and China-Japan-Korea Summit on Natural Products(第七届国际后基因组技术论坛及中日韩天然产物论坛 IFPT)

重庆

英文

35-36

2011-10-28(万方平台首次上网日期,不代表论文的发表时间)