A new and general synthesis of a porphyrinK(Ⅰ) with two alkoxyl linkages is described. The synthesis involves the reaction of dibromopropane with phenolic porphyrin to form ω-bromopropylporphyrin ether. This ether t...A new and general synthesis of a porphyrinK(Ⅰ) with two alkoxyl linkages is described. The synthesis involves the reaction of dibromopropane with phenolic porphyrin to form ω-bromopropylporphyrin ether. This ether then reacts with another phenolic porphyrin to give the target compounds. The properties of the target compounds were confirmed by means of elemental analysis, UV-Vis, IR, and ~ 1H NMR spectroscopies. Their spectral properties and thermal stability were also studied.展开更多
A palladium catalyzed ortho-alkoxylation of aryl C-H bond was accomplished with primary and secondary alcohols as alkoxylation reagents and with triazole as new directing group.This transformation has a good functiona...A palladium catalyzed ortho-alkoxylation of aryl C-H bond was accomplished with primary and secondary alcohols as alkoxylation reagents and with triazole as new directing group.This transformation has a good functional group tolerance and is not sensitive to moisture and air.展开更多
With the support by the National Natural Science Foundation of China,the research group led by Prof.Chen Yiyun(陈以昀)from Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences demonstrates that the dono...With the support by the National Natural Science Foundation of China,the research group led by Prof.Chen Yiyun(陈以昀)from Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences demonstrates that the donor-acceptor complex enables metal-free inert bond functionalizations,which was published in Angew Chem Int Ed(2017,56(41):12619-12623).展开更多
Under iodine-catalyzed and visible light-irradiated aerobic conditions, selenoalkoxylation of olefins with diselenides and alcohols can be efficiently achieved to afford the useful α-alkoxyl selenides in the presence...Under iodine-catalyzed and visible light-irradiated aerobic conditions, selenoalkoxylation of olefins with diselenides and alcohols can be efficiently achieved to afford the useful α-alkoxyl selenides in the presence of only 0.5 equiv. of H_2O_2. Controlling the sub-stoichiometric H_2O_2 amount is crucial to avoid the non-selective over-oxidation of the diselenides that leads to the ineffective hyper-valent selenium compounds. Meanwhile, under visible light irradiation, the green, safe, and low-cost air can work as a supplemental mild oxidant in the reaction to ensure selective oxidation of the diselenides, full conversion of the reactants, and ultimately good yield of the products.展开更多
文摘A new and general synthesis of a porphyrinK(Ⅰ) with two alkoxyl linkages is described. The synthesis involves the reaction of dibromopropane with phenolic porphyrin to form ω-bromopropylporphyrin ether. This ether then reacts with another phenolic porphyrin to give the target compounds. The properties of the target compounds were confirmed by means of elemental analysis, UV-Vis, IR, and ~ 1H NMR spectroscopies. Their spectral properties and thermal stability were also studied.
基金Support of this work by the“973”Project from the MOST of China(2015CB856600)NSFC(No.21332001)is gratefully acknowledged.
文摘A palladium catalyzed ortho-alkoxylation of aryl C-H bond was accomplished with primary and secondary alcohols as alkoxylation reagents and with triazole as new directing group.This transformation has a good functional group tolerance and is not sensitive to moisture and air.
文摘With the support by the National Natural Science Foundation of China,the research group led by Prof.Chen Yiyun(陈以昀)from Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences demonstrates that the donor-acceptor complex enables metal-free inert bond functionalizations,which was published in Angew Chem Int Ed(2017,56(41):12619-12623).
基金supported by the National Natural Science Foundation of China(21202141,21672069)Priority Academic Program Development of Jiangsu Higher Education Institutions+1 种基金the Open Project Program of Jiangsu Key Laboratory of Zoonosis(R1509)the High Level Talent Support Project of Yangzhou University
文摘Under iodine-catalyzed and visible light-irradiated aerobic conditions, selenoalkoxylation of olefins with diselenides and alcohols can be efficiently achieved to afford the useful α-alkoxyl selenides in the presence of only 0.5 equiv. of H_2O_2. Controlling the sub-stoichiometric H_2O_2 amount is crucial to avoid the non-selective over-oxidation of the diselenides that leads to the ineffective hyper-valent selenium compounds. Meanwhile, under visible light irradiation, the green, safe, and low-cost air can work as a supplemental mild oxidant in the reaction to ensure selective oxidation of the diselenides, full conversion of the reactants, and ultimately good yield of the products.
基金supported by USTC Research Funds of the Double First-Class Initiative(YD2060002024)Youth Innovation Promotion Association CAS(2020448)+2 种基金National Natur-al Science Foundation of China(22171254)Anhui Provincial Natural Science Foundation(2108085MB58)Start-up Research Fund from University of Science and Technology of China(KY2060000216).
