Alcohols as alkylating agents in heteroarene C-H functionalization

作者：Jin, Jian; MacMillan, David W. C.^*

来源：Nature, 2015, 525(7567): 87-90.

DOI：10.1038/nature14885

• POLARITY-REVERSAL CATALYSIS
• PHOTOREDOX CATALYSIS
• DIRECT ARYLATION
• BONDS
• RACEMIZATION
• ACTIVATION
• DISCOVERY
• STRATEGY
• ETHERS

Redox processes and radical intermediates are found in many biochemical processes, including deoxyribonucleotide synthesis and oxidative DNA damage(1). One of the core principles underlying DNA biosynthesis is the radical-mediated elimination of H2O to deoxygenate ribonucleotides, an example of 'spin-centre shift'(2), during which an alcohol C-O bond is cleaved, resulting in a carbon-centred radical intermediate. Although spin-centre shift is a well-understood biochemical process, it is underused by the synthetic organic chemistry community. We wondered whether it would be possible to take advantage of this naturally occurring process to accomplish mild, non-traditional alkylation reactions using alcohols as radical precursors. Because conventional radical-based alkylation methods require the use of stoichiometric oxidants, increased temperatures or peroxides(3-7), a mild protocol using simple and abundant alkylating agents would have considerable use in the synthesis of diversely functionalized pharmacophores. Here we describe the development of a dual catalytic alkylation of heteroarenes, using alcohols as mild alkylating reagents. This method represents the first, to our knowledge, broadly applicable use of unactivated alcohols as latent alkylating reagents, achieved via the successful merger of photoredox and hydrogen atom transfer catalysis. The value of this multi-catalytic protocol has been demonstrated through the late-stage functionalization of the medicinal agents, fasudil and milrinone.

• 出版日期2015-9-3