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Total Syntheses of Discoipyrroles A, B, and C, Three Marine Natural Products
The Journal of Organic Chemistry ( IF 3.6 ) Pub Date : 2024-04-10 , DOI: 10.1021/acs.joc.4c00462
Gaurav G. Dake 1 , Krishna P. Kaliappan 1
Affiliation  

Herein, we describe our efforts culminating in the total syntheses of discoipyrroles A, B, and C in 6, 6, and 7 steps respectively with excellent overall yield. Total syntheses of these unique natural products have been accomplished involving microwave-mediated Paal–Knorr pyrrole synthesis, Pd-catalyzed carbonylative transformation, and MoOPH (Vedejs reagent) oxidation as key reactions to construct the 1,2,3,5-tetrasubstituted pyrrole and oxidative cyclization of highly substituted pyrrole as key steps.

中文翻译:

三种海洋天然产物二吡咯 A、B、C 的全合成

在此,我们描述了我们的努力,最终分别通过 6、6 和 7 步全合成二吡咯 A、B 和 C,并具有优异的总产率。这些独特的天然产物的全合成已经完成,涉及微波介导的Paal-Knorr吡咯合成、Pd催化的羰基化转化和MoOPH(Vedejs试剂)氧化作为构建1,2,3,5-四取代吡咯和高取代吡咯的氧化环化是关键步骤。
更新日期:2024-04-10
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