Radical chain repair: The hydroalkylation of polysubstituted unactivated alkenes
Author(s) -
Guillaume Povie,
Sankar Rao Suravarapu,
Martin P. Bircher,
Melinda Meyer Mojzes,
Samuel Rieder,
Philippe Renaud
Publication year - 2018
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.aat6031
Subject(s) - scope (computer science) , process (computing) , chemistry , radical , business , computer science , risk analysis (engineering) , biochemical engineering , combinatorial chemistry , organic chemistry , engineering , programming language
The concept of repair is widely used by nature to heal molecules such as proteins, lipids, sugars, and DNA that are damaged by hydrogen atom abstraction resulting from oxidative stress. We show that this strategy, rather undocumented in the field of synthetic organic chemistry, can be used in a radical chain reaction to enable notoriously intractable transformations. By overcoming the radical chain inhibitor properties of substituted alkenes, the radical-mediated hydroalkylation of mono-, di-, tri-, and even tetrasubstituted unactivated olefins could be performed under mild conditions. With a remarkable functional group tolerance, this reaction provides a general coupling method for the derivatization of olefin-containing natural products.
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