| Literature DB >> 30636411 |
Hugh Nakamura1, Kosuke Yasui1, Yuzuru Kanda1, Phil S Baran1.
Abstract
A unified and modular approach to the teleocidin B family of natural products is presented that proceeds in 11 steps and features an array of interesting strategies and methods. Indolactam V, the known biosynthetic precursor to this family, was accessed through electrochemical amination, Cu-mediated aziridine opening, and a remarkable base-induced macrolactamization. Guided by a desire to minimize concession steps, the tactical combination of C-H borylation and a Sigman-Heck transform enabled the convergent, stereocontrolled synthesis of the teleocidins.Entities:
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Year: 2019 PMID: 30636411 PMCID: PMC6353666 DOI: 10.1021/jacs.8b13697
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419