| Literature DB >> 30575396 |
Chi He1, Thomas P Stratton1, Phil S Baran1.
Abstract
A simple total synthesis of herqulines B and C is reported, modeled on the reductive biosynthesis reported previously by other researchers. Commencing from tyrosine, these alkaloids were fashioned through a dimerization, macrocyclization, and four consecutive reductions. Emerging from these studies are strategic insights on the synthesis of these strained alkaloids, as well as mild conditions for the exhaustive reduction of diketopiperizines.Entities:
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Year: 2018 PMID: 30575396 PMCID: PMC6475496 DOI: 10.1021/jacs.8b13029
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419