Journal
CURRENT ORGANIC CHEMISTRY
Volume 15, Issue 17, Pages 3077-3090Publisher
BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/138527211798357182
Keywords
alpha-functionalized aldehydes; N-heterocyclic carbenes; organocatalysis; redox reaction; enantioselectivity; umpolung; ring-expansion
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Funding
- National Natural Science Foundation of China [20732006, 20821002, 20972177]
- National Basic Research Program of China (973 Program) [2009CB825300]
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This review summarizes the recent advances on the redox reactions involving alpha-functionalized aldehydes catalyzed by N-heterocyclic carbenes. In the presence of N-heterocyclic carbene, alpha-functionalized aldehydes such as alpha-haloaldehydes, alpha-ring-fused aldehydes, alpha-aryloxyacetaldehydes and alpha-aroyloxyaldehydes undergo the redox reactions affording novel reaction types.
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