[1] Ciamician G. The photochemistry of the future[J]. Science, 1912, 36:385-394.
[2] Narayanam J M R, Stephenson C R J. Visible light photoredox catalysis:applications in organic synthesis[J]. Chemical Society Review, 2011, 40:102-113.
[3] Xuan J, Xiao W J. Visible light photoredox catalysis[J]. Angewandte Chemie International Edition, 2012, 51:6828-6838.
[4] Xi Y M, Yi H, Lei A W. Synthetic applications of photoredox catalysis with visible light[J]. Organic & Biomolecular Chemistry, 2013, 11:2387-2403.
[5] Prier C K, Rankic D A, MacMillan D W C. Visible light photoredox catalysis with transition metal complexes:applications in organic synthesis[J]. Chemical Review, 2013, 113:5322-5363.
[6] Lang X J, Zhao J C, Chen X D. Cooperative photoredox catalysis[J]. Chemical Society Review, 2016, 45:3026-3038.
[7] Ravelli D, Protti S, Fagnoni M. Carbon-carbon bond forming reactions via photogenerated intermediates[J]. Chemical Review, 2016, 116:9850-9913.
[8] Romero N A, Nicewicz D A. Organic photoredox catalysis[J]. Chemical Review, 2016, 116:10075-10166.
[9] Skubi K L, Blum T R, Yoon T P. Dual catalysis strategies in photochemical synthesis[J]. Chemical Review, 2016, 116:10035-10074.
[10] Lang X J, Ma W H, Chen C C, Ji H W, Zhao J C. Selective aerobic oxidation mediated by TiO2 photocatalysis[J]. Accounts of Chemical Research, 2014, 47:355-363.
[11] Li X B, Li Z J, Gao Y J, Meng Q Y, Yu S, Weiss R G, Tung C H, Wu L Z. Mechanistic insights into the interface-directed transformation of thiols into disulfides and molecular hydrogen by visible-light irradiation of quantum dots[J]. Angewandte Chemie International Edition, 2014, 53:2085-2089.
[12] Wang Y, Wang X C, Antonietti M. Polymeric graphitic carbon nitride as a heterogeneous organocatalyst:from photochemistry to multipurpose catalysis to sustainable chemistry[J]. Angewandte Chemie International Edition, 2012, 51:68-89.
[13] Jang M, Cai L, Udeani G O, Slowing K V, Thomas C F, Beecher C W W, Fong H H S, Farnsworth N R, Kinghorn A D, Mehta R G, Moon R C, Pezzuto J M. Cancer chemopreventive activity of resveratrol, a natural product derived from grapes[J]. Science, 1997, 275:218-220.
[14] Celaje J A, Zhang D, Guerrero A M, Selke M. Chemistry of trans-resveratrol with singlet oxygen:[2+2] addition,[4+2] addition, and formation of the phytoalexin moracin M[J]. Organic Letters, 2011, 13:4846-4849.
[15] Song T, Zhou B, Peng G W, Zhang Q B, Wu L Z, Liu Q, Wang Y. Aerobic oxidative coupling of resveratrol and its analogues by visible light using mesoporous graphitic carbon nitride (mpg-C3N4) as a bioinspired catalyst[J]. Chemistry-A European Journal, 2014, 20:678-682.
[16] Zhang Z Q, Ji S J, Lu J, Yang J M. A mild and efficient synthesis of 5-Oxo-5,6,7,8-tetrahydro-4H benze-[b]-pyran derivatives in room temperature ionic liquids[J]. Chinese Journal of Chemistry, 2005, 23:1085-1089.
[17] Mitsunobu O, Matsumoto S, Wada M, Masuda H. Photooxidation of 1,4-dihydropyridine[J]. Bulletin of the Chemical Society of Japan, 1972, 45:1453-1457.
[18] Memarian H R, Sadeghi M M, Momeni A R, D pp D. Synthesis and photo-chemistry of novel 3,5-diacetyl-1,4-dihydropyridines[J]. Monatshefte Für Chemie, 2002, 133:661-667.
[19] Fang X Q, Liu Y C, Li C Z. 9-Phenyl-10-methylacridi-nium:a highly efficient and reusable organocatalyst for mild aromatization of 1,4-dihydro-pyridines by molecular oxygen[J]. The Journal of Organic Chemistry, 2007, 72:8608-8610.
[20] Wang D H, Liu Q, Cheng B, Zhang L P, Tung C H, Wu L Z. Photooxidation of Hantzsch 1,4-dihydropyridines by molecular oxygen[J]. Chinese Science Bulletin, 2010, 55:2855-2858.
[21] Liu Q, Li Y N, Zhang H H, Chen B, Tung C H, Wu L Z. Reactivity and mechanistic insight into visible-light-induced aerobic cross-dehydrogenative coupling reaction by organophotocatalysts[J]. Chemistry-A European Journal, 2012, 18:620-627.
[22] Wei X J, Wang L, Jia W L, Du S F, Wu L Z, Liu Q. Metal-free-mediated oxidation aromatization of 1,4-dihydropyridines to pyridines using visible light and air[J]. Chinese Journal of Chemistry, 2014, 32:1245-1250.
[23] Wang L, Ma Z G, Wei X J, Meng Q Y, Yang D T, Du S F, Chen Z F, Wu L Z, Liu Q. Synthesis of 2-substituted pyrimidines and benzoxazoles via a visible-light-driven organocatalytic aerobic oxidation:enhancement of the reaction rate and selectivity by a base[J]. Green Chemistry, 2014, 16:3752-3757.
[24] Griesbeck A G, Cho M. 9-Mesityl-10-methylacridinium:an efficient type Ⅱ and electron-transfer photooxygenation catalyst[J]. Organic Letters, 2007, 9:611-613.
[25] Lechner R, Kümmel S, K nig B. Visible light flavin photo-oxidation of methyl-benzenes, styrenes and phenylacetic acids[J]. Photochemical & Photobiological Sciences, 2010, 9:1367-1377.
[26] Zhang P F, Wang Y, Yao J, Wang C M, Yan C, Anto-nietti M, Li H R. Visible-light-induced metal-free allylic oxidation utilizing a coupled photo-catalytic system of g-C3N4 and N-hydroxy compounds[J]. Advanced Synthesis & Catalysis, 2011, 353:1447-1451.
[27] Su Y J, Zhang L R, Jiao N. Utilization of natural sunlight and air in the aerobic oxidation of benzyl halides[J]. Organic Letters, 2011, 13:2168-2171.
[28] Fukuzumi S, Kotani H, Ohkubo K, Ogo S, Tkachenko N V, Lemmetyinen H. Electron-transfer state of 9-mesityl-10-methylacridinium ion with a much longer lifetime and higher energy than that of the natural photosynthetic reaction center[J]. Journal of the American Chemical Society, 2004, 126:1600-1601.
[29] Perkowski A J, Nicewicz D A. Direct catalytic anti-Mar-kovnikov addition of carboxylic acids to alkenes[J]. Journal of the American Chemical Society, 2013, 135:10334-10337.
[30] Zeng T T, Xuan J, Ding W, Wang K, Lu L Q, Xiao W J.[3+2] Cycloaddition/oxidative aromatization sequence via photoredox catalysis:one-pot synthesis of oxazoles from 2H-azirines and aldehydes[J]. Organic Letters, 2015, 17:4070-4073.
[31] Ramirez N P, Bosque I, Gonzalez-Gomez J C. Photocatalytic dehydrogenative lactonization of 2-arylbenzoic acids[J]. Organic Letters, 2015, 17:4550-4553.
[32] Hering T, Slanina T, Hancock A, Wille U, K nig B. Visible light photooxidation of nitrate:the dawn of a nocturnal radical[J]. Chemical Communications, 2015, 51:6568-6571.
[33] Yi H, Bian C L, Hu X, Niu L B, Lei A W. Visible light mediated efficient oxidative benzylic sp3 C-H to ketone derivatives obtained under mild conditions using O2[J]. Chemical Communications, 2015, 51:14046-14049.
[34] Wang K, Meng L G, Zhang Q, Wang L. Direct construction of 4-aryl tetralones via visible-light-induced cyclization of styrenes with molecular oxygen[J]. Green Chemistry, 2016, 18:2864-2870.
[35] Kotani H, Ohkubo K, Fukuzumi S. Photocatalytic oxygenation of anthracens and olefins with dioxygen via selective radical coupling using 9-mesityl-10-methylacridinium ion as an effective electron-transfer photocatalyst[J]. Journal of the American Chemical Society, 2004, 126:15999-16006.
[36] Zhang Q B, Ban Y L, Zhou D G, Zhou P P, Wu L Z, Liu Q. Preparation of α-acyloxy ketones via visible-light-driven aerobic oxo-acyloxylation of olefins with carboxylic acids[J]. Organic Letters, 2016, 18:5256-5259.
[37] Badary O A, Taha R A, El-Din A M G, Abdel-Wahab M H. Thymoquinone is a potent superoxide anion scavenger[J]. Drug and Chemical Toxicology, 2003, 26:87-98. |