Access to benzene-modified 2nd generation strigolactams and GR24 by merging C–H olefination with decarboxylative Giese cyclization

Abstract

Herein, we reported an efficient and general synthetic route to assemble benzene-modified 2^nd generation strigolactams and GR24. The key features of this synthesis include a palladium-catalyzed ortho-selective olefination of the commercially available substituted N-Boc phenylalanine and a decarboxylative Giese radical cyclization. The bioactivities of these compounds to stimulate the seed germination of Orobanche aegyptiaca parasitic weed were also analysed. 2^nd generation strigolactam 15f derived from para-OMe phenylalanine showed superior bioactivity to the original unsubstituted 15b.