| Literature DB >> 33983721 |
Masato Saito1, Yu Kawamata1, Michael Meanwell1, Rafael Navratil1, Debora Chiodi1, Ethan Carlson1, Pengfei Hu1, Longrui Chen1, Sagar Udyavara2, Cian Kingston3, Mayank Tanwar2, Sameer Tyagi4, Bruce P McKillican4, Moses G Gichinga4, Michael A Schmidt5, Martin D Eastgate5, Massimiliano Lamberto6, Chi He1, Tianhua Tang3, Christian A Malapit3, Matthew S Sigman3, Shelley D Minteer3, Matthew Neurock2, Phil S Baran1.
Abstract
The site-specific oxidation of strong C(sp3)-H bonds is of uncontested utility in organic synthesis. From simplifying access to metabolites and late-stage diversification of lead compounds to truncating retrosynthetic plans, there is a growing need for new reagents and methods for achieving such a transformation in both academic and industrial circles. One main drawback of current chemical reagents is the lack of diversity with regard to structure and reactivity that prevents a combinatorial approach for rapid screening to be employed. In that regard, directed evolution still holds the greatest promise for achieving complex C-H oxidations in a variety of complex settings. Herein we present a rationally designed platform that provides a step toward this challenge using N-ammonium ylides as electrochemically driven oxidants for site-specific, chemoselective C(sp3)-H oxidation. By taking a first-principles approach guided by computation, these new mediators were identified and rapidly expanded into a library using ubiquitous building blocks and trivial synthesis techniques. The ylide-based approach to C-H oxidation exhibits tunable selectivity that is often exclusive to this class of oxidants and can be applied to real-world problems in the agricultural and pharmaceutical sectors.Entities:
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Year: 2021 PMID: 33983721 PMCID: PMC8718116 DOI: 10.1021/jacs.1c03780
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419