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Diversification of Monoterpene Indole Alkaloid Analogs through Cross-Coupling
Catharanthus roseus monoterpene indole alkaloid analogs have been produced via a combination of biosynthetic and chemical strategies. Specifically, introduction of a chemical handlea chlorine or a bromineinto the target molecule by mutasynthesis, followed by postbiosynthetic chemical derivatizatio...
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Published in: | Organic letters 2013-06, Vol.15 (11), p.2850-2853 |
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container_issue | 11 |
container_start_page | 2850 |
container_title | Organic letters |
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creator | Runguphan, Weerawat O’Connor, Sarah E |
description | Catharanthus roseus monoterpene indole alkaloid analogs have been produced via a combination of biosynthetic and chemical strategies. Specifically, introduction of a chemical handlea chlorine or a bromineinto the target molecule by mutasynthesis, followed by postbiosynthetic chemical derivatization using Pd-catalyzed Suzuki-Miyaura cross-coupling reactions robustly afforded aryl and heteroaryl analogs of these alkaloids. |
doi_str_mv | 10.1021/ol401179k |
format | article |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Bromine - chemistry Catalysis Chlorine - chemistry Cross-Linking Reagents - chemistry Heterocyclic Compounds - chemical synthesis Heterocyclic Compounds - chemistry Indole Alkaloids - chemical synthesis Indole Alkaloids - chemistry Indole Alkaloids - metabolism Molecular Structure Monoterpenes - chemical synthesis Monoterpenes - chemistry |
title | Diversification of Monoterpene Indole Alkaloid Analogs through Cross-Coupling |
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