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Cobalt bis(acetylacetonate)-tert-butyl hydroperoxide-triethylsilane: a general reagent combination for the Markovnikov-selective hydrofunctionalization of alkenes by hydrogen atom transfer.


ABSTRACT: We show that cobalt bis(acetylacetonate) [Co(acac)2], tert-butyl hydroperoxide (TBHP), and triethylsilane (Et3SiH) constitute an inexpensive, general, and practical reagent combination to initiate a broad range of Markovnikov-selective alkene hydrofunctionalization reactions. These transformations are believed to proceed by cobalt-mediated hydrogen atom transfer (HAT) to the alkene substrate, followed by interception of the resulting alkyl radical intermediate with a SOMOphile. In addition, we report the first reductive couplings of unactivated alkenes and aryldiazonium salts by an HAT pathway. The simplicity and generality of the Co(acac)2-TBHP-Et3SiH reagent combination suggests it as a useful starting point to develop HAT reactions in complex settings.

SUBMITTER: Ma X 

PROVIDER: S-EPMC6122341 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature

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Cobalt bis(acetylacetonate)-<i>tert</i>-butyl hydroperoxide-triethylsilane: a general reagent combination for the Markovnikov-selective hydrofunctionalization of alkenes by hydrogen atom transfer.

Ma Xiaoshen X   Herzon Seth B SB  

Beilstein journal of organic chemistry 20180828


We show that cobalt bis(acetylacetonate) [Co(acac)<sub>2</sub>], <i>tert</i>-butyl hydroperoxide (TBHP), and triethylsilane (Et<sub>3</sub>SiH) constitute an inexpensive, general, and practical reagent combination to initiate a broad range of Markovnikov-selective alkene hydrofunctionalization reactions. These transformations are believed to proceed by cobalt-mediated hydrogen atom transfer (HAT) to the alkene substrate, followed by interception of the resulting alkyl radical intermediate with a  ...[more]

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