Stereoselective (4 + 3) cycloadditions of allenyl ethersfurans by chiral auxiliaries inducing and evaluation of antibreast cancer activity.

Autor: Wenli Lei, Yuyang Song, Ai Long, Yanyan Que, Shuzhong He, Hang Zhong, Yang Chen
Předmět:
Zdroj: Frontiers in Plant Science; 12/21/2022, Vol. 13, p1-10, 10p
Abstrakt: The medicinal plants were wildly library of natural products in drug discovery. The most active molecules with seven-membered rings skeleton represent a challenge for construction. A stereoselectivity (4 + 3) cycloadditions between allenyl ethers and substituted furans induced by chiral auxiliaries has been investigated. And the results showed significant stereoselectivities and regioselectivities. The optical cycloadducts with an oxygen-substituted seven-membered ring framework were generated by removing chiral auxiliaries under acidic conditions. The antiproliferative activity of the novel compounds displayed moderate antiproliferative effects toward T47D cells. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index