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Cobalt‐Catalyzed Hydrogen‐Atom Transfer Induces Bicyclizations that Tolerate Electron‐Rich and Electron‐Deficient Intermediate Alkenes
Author(s) -
Vrubliauskas Darius,
Vanderwal Christopher D.
Publication year - 2020
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.202000252
Subject(s) - nitrile , chemistry , catalysis , cobalt , hydrogen atom , electron transfer , polyene , photochemistry , solvent , metal , combinatorial chemistry , medicinal chemistry , organic chemistry , alkyl
A novel Co II ‐catalyzed polyene cyclization was developed that is uniquely effective when performed in hexafluoroisopropanol as the solvent. The process is presumably initiated by metal‐catalyzed hydrogen‐atom transfer (MHAT) to 1,1‐disubstituted or monosubstituted alkenes, and the reaction is remarkable for its tolerance of internal alkenes bearing either electron‐rich methyl or electron‐deficient nitrile substituents. Electron‐rich aromatic terminators are required in both cases. Terpenoid scaffolds with different substitution patterns are obtained with excellent diastereoselectivities, and the bioactive C20‐oxidized abietane diterpenoid carnosaldehyde was made to showcase the utility of the nitrile‐bearing products. Also provided are the results of several mechanistic experiments that suggest the process features an MHAT‐induced radical bicyclization with late‐stage oxidation to regenerate the aromatic terminator.