作者:Joseph W. Tucker、Yuan Zhang、Timothy F. Jamison、Corey R. J. Stephenson
DOI:10.1002/anie.201200961
日期:2012.4.23
Photoredoxcatalysis: A variety of organic transformations mediated by visible‐light‐active photoredox catalysts have been conducted in a photochemical flow reactor. The reactor design is very simple and can be easily implemented in any laboratory (see picture). In addition, this reactor afforded a marked increase in the reaction rate compared to those observed in typical batch (round bottom flask)
Perkin–Markovnikov Type Reaction Initiated with Electrogenerated Superoxide Ion
作者:Fumihiro Ojima、Tetsuo Osa
DOI:10.1246/bcsj.62.3187
日期:1989.10
The cyclic condensation of active methylene compounds such as diethyl malonate, dimethyl malonate, ethyl acetoacetate, or acetylacetone and dibromoalkanes such as 1,2-dibromoethane, 1,3-dibromopropane, 1,4-dibromobutane, 1,5-dibromopentane, 1,6-dibromohexane, 1,3-dibromobutane, or 1,4-dibromopentane with electrogenerated superoxide ion was studied electrochemically in N,N-dimethylformamide (DMF) using cyclic voltammetry (CV) and controlled potential macro-electrolysis. The CV shows that electrogenerated superoxide ion reacts with both active methylene compounds and dibromoalkanes in the dissolved oxygen medium. Controlled potential macro-electrolysis of the above components generally yielded cycloalkanes as the main products. In comparison, the chemical method using sodium ethoxide was also carried out. Two reaction mechanisms via the proton abstraction of active methylene compounds with electrogenerated superoxide ion and via the nucleophilic attack of the superoxide ion on dibromoalkanes are presented.
Tin-free radical cyclization reactions initiated by visible light photoredox catalysis
作者:Joseph W. Tucker、John D. Nguyen、Jagan M. R. Narayanam、Scott W. Krabbe、Corey R. J. Stephenson
DOI:10.1039/c0cc00981d
日期:——
Herein, we report an advancement in the application of visiblelight photoredox catalysts in a classic free radicalmediated reaction, cyclization onto unactivated pi-systems. The reactive radical intermediate is generated by the single electron reduction of an activated C-Br bond by an electron-rich redox catalyst afforded by a visiblelight induced catalytic cycle.
Mesoporous graphitic carbonnitride (mpg‐C3N4) was found to be an efficient heterogeneous photocatalyst for the metal‐free radical cyclization of 2‐bromo‐1,3‐dicarbonyl compounds. Reactions leading to functionalized cyclopentanes proceed under mild conditions and can be conducted in a continuous flow photoreactor. Compared to the batch reaction, the use of a continuous flow reactor resulted in a significant
发现介孔石墨碳氮化物(mpg-C 3 N 4)是2-溴-1,3-二羰基化合物的金属自由基环化的有效多相光催化剂。导致官能化的环戊烷的反应在温和的条件下进行,可以在连续流动的光反应器中进行。与分批反应相比,使用连续流动反应器可显着减少反应时间(4小时后,批次中0.04 mmol底物的完全转化,而在流动反应器中,相同量的底物可以完全转化)在40分钟内转化为产品)。该反应的机理研究表明,THF不仅起溶剂的作用,而且还是至关重要的氢和电子给体。
Cerium (IV) ammonium nitrate promoted oxidative cyclization of dimethyl 4-pentenylmalonate
作者:Enrico Baciocchi、Anna Belli Paolobelli、Renzo Ruzziconi
DOI:10.1016/s0040-4020(01)81235-7
日期:1992.1
CAN promoted oxidative cyclization of dimethyl 4-pentenylmalonate has been investigated in MeOH and in AcOH. The product distribution and the regioselectivity of the reaction (5-exo/6-endo ratio) appear to be very sensitive to the reaction conditions as well as the presence and the nature of copper salts, which can also be exploited from the synthetic point of view.