Abstract
The first total synthesis of marine natural product, (±)- marinopyrrole A, has been accomplished via a nine-step synthesis in an overall yield of 30%. A small focused library based on marinopyrrole has been designed and synthesized. The scope of chemistry was investigated, and a robust chemistry suitable for library synthesis has been developed in the current study. The method that we have developed has made it possible to generate diverse analogues based on structurally novel marinopyrroles for study of potential antibiotic and anticancer activities.
Original language | English (US) |
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Pages (from-to) | 541-547 |
Number of pages | 7 |
Journal | Journal of Combinatorial Chemistry |
Volume | 12 |
Issue number | 4 |
DOIs | |
State | Published - Jul 12 2010 |
Externally published | Yes |
ASJC Scopus subject areas
- General Chemistry