Double Annulative Cascade of Tryptophan-Containing Peptides Triggered by Selectfluor
摘要:
A common dearomative strategy toward the kapakahines B/F and chaetominine natural products is reported. The proposed biomimetic strategy generates the tetracyclic alpha-carboline core in a single step, featuring a selectfluor-mediated dearomatization of preactivated N-Phth-Trp-Xaa-OR dipeptides at the C-terminus. The pivotal cascade includes a double annulation and the formation of three carbon-heteroatom bonds while gaining, for the first time, some insight on the diastereoselectivity outcome during the formation of the alpha-carboline fragment.
Double Annulative Cascade of Tryptophan-Containing Peptides Triggered by Selectfluor
作者:Bret Tréguier、Stéphane P. Roche
DOI:10.1021/ol403281t
日期:2014.1.3
A common dearomative strategy toward the kapakahines B/F and chaetominine natural products is reported. The proposed biomimetic strategy generates the tetracyclic alpha-carboline core in a single step, featuring a selectfluor-mediated dearomatization of preactivated N-Phth-Trp-Xaa-OR dipeptides at the C-terminus. The pivotal cascade includes a double annulation and the formation of three carbon-heteroatom bonds while gaining, for the first time, some insight on the diastereoselectivity outcome during the formation of the alpha-carboline fragment.