Photo-NHC Catalysis: Accessing Ketone Photochemistry with Carboxylic Acid Derivatives

被引:6
作者
Hopkinson, Matthew N. [1 ]
Mavroskoufis, Andreas [1 ]
机构
[1] Free Univ Berlin, Inst Chem & Biochem, Fabeckstr 34-36, D-14195 Berlin, Germany
关键词
photochemistry; N-heterocyclic carbenes; organocatalysis; photoenolization; acid fluorides; annulation; cycloaddition; carbonyls; N-HETEROCYCLIC CARBENE; O-QUINODIMETHANES; DUAL CATALYSIS; ALKYLATION; DRIVEN; ORGANOCATALYSIS; IMINIUM; PHOTOCATALYSIS; STRATEGIES; THIOUREA;
D O I
10.1055/s-0040-1706472
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Excitation of carbonyl groups is one of the most widely employed activation modes in photochemistry. Many synthetically important transformations, however, are successful only with aldehydes and ketones; substrates at the carboxylic acid oxidation level remain underrepresented. We have developed a conceptually novel strategy for enabling 'ketone-like' photochemistry with carboxylic acid derivatives that employs an N-heterocyclic carbene (NHC) organocatalyst. Using this 'Photo-NHC' catalysis approach, a proof-of-concept photoenolization/Diels-Alder (PEDA) reaction between acid fluorides and trifluoroacetophenones was developed. Stoichiometric studies and TD-DFT calculations supported a mechanistic scenario in which the NHC influences the absorption wavelength and inherent photochemical reactivity of the carbonyl group during the catalytic cycle.
引用
收藏
页码:95 / 101
页数:7
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