Visible-light-induced decarboxylative alkynylation of carboxylic acids in batch and continuous flow

Gallezot, 2012, Chem. Soc. Rev., 41, 1538, 10.1039/C1CS15147A Rodríguez, 2011, Chem. Soc. Rev., 40, 5030, 10.1039/c1cs15093f Liu, 2021, Green Synth. Catal., 2, 389, 10.1016/j.gresc.2021.10.003 Dzik, 2012, Chem. Sci., 3, 2671, 10.1039/c2sc20312j Wang, 2013, Adv. Synth. Catal., 355, 2745, 10.1002/adsc.201300375 Dai, 2013, Chin. J. Org. Chem., 33, 2460, 10.6023/cjoc201307014 Nicewicz, 2008, Science, 322, 77, 10.1126/science.1161976 Huang, 2016, ACS Catal., 6, 4983, 10.1021/acscatal.6b01379 Xuan, 2015, Angew. Chem., Int. Ed., 54, 15632, 10.1002/anie.201505731 Luo, 2016, ACS Catal., 6, 873, 10.1021/acscatal.5b02204 McTiernan, 2017, ACS Catal., 7, 2171, 10.1021/acscatal.6b03687 Zuo, 2014, J. Am. Chem. Soc., 136, 5257, 10.1021/ja501621q Noble, 2018, Angew. Chem. Int. Ed., 57, 2155, 10.1002/anie.201712186 Yue, 2020, Angew. Chem., Int. Ed., 59, 5738, 10.1002/anie.201914061 Shirase, 2020, J. Am. Chem. Soc., 142, 5668, 10.1021/jacs.9b12918 Lovett, 2016, Org. Lett., 18, 3494, 10.1021/acs.orglett.6b01712 Cao, 2018, J. Am. Chem. Soc., 140, 16360, 10.1021/jacs.8b11218 Vaillant, 2017, Chem. Sci., 8, 1790, 10.1039/C6SC04907A Chen, 2019, Org. Lett., 21, 2130, 10.1021/acs.orglett.9b00443 Johnston, 2016, Nature, 536, 322, 10.1038/nature19056 Pieber, 2019, Angew. Chem., Int. Ed., 58, 9575, 10.1002/anie.201902785 Huang, 2015, Angew. Chem. Int. Ed., 54, 7872, 10.1002/anie.201502369 Yoshimura, 2016, Chem. Rev., 116, 3328, 10.1021/acs.chemrev.5b00547 Zhou, 2015, Angew. Chem. Int. Ed., 54, 11196, 10.1002/anie.201504559 Le Vaillant, 2015, Angew. Chem. Int. Ed., 54, 11200, 10.1002/anie.201505111 Hari, 2014, Chem. Commun., 50, 6688, 10.1039/C4CC00751D Wang, 2020, Green Synth. Catal., 1, 42, 10.1016/j.gresc.2020.05.003 Ghosh, 2017, Angew. Chem. Int. Ed., 56, 8544, 10.1002/anie.201703004 Yang, 2016, J. Org. Chem., 81, 12357, 10.1021/acs.joc.6b02385 Garreau, 2019, J. Waser. Angew. Chem. Int. Ed., 58, 8182, 10.1002/anie.201901922 Gao, 2020, Adv. Synth. Catal., 362, 3898, 10.1002/adsc.202000777 Feng, 2013, Org. Lett., 15, 1472, 10.1021/ol400197y Tan, 2015, Angew. Chem. Int. Ed., 54, 8374, 10.1002/anie.201503479 Huang, 2017, Angew. Chem. Int. Ed., 56, 11901, 10.1002/anie.201706781 Okada, 1991, J. Am. Chem. Soc., 113, 9401, 10.1021/ja00024a074 Okada, 1992, Tetrahedron Lett., 33, 7377, 10.1016/S0040-4039(00)60192-2 Schnermann, 2012, Angew. Chem. Int. Ed., 51, 9576, 10.1002/anie.201204977 Lackner, 2013, J. Am. Chem. Soc., 135, 15342, 10.1021/ja408971t Yang, 2015, Chem. Commun., 51, 5275, 10.1039/C4CC06344A Zhu, 2021, ACS Catal., 11, 6334, 10.1021/acscatal.1c01600 Xia, 2020, Angew. Chem. Int. Ed., 59, 16926, 10.1002/anie.202006317 Zhang, 2017, Org. Lett., 19, 1016, 10.1021/acs.orglett.6b03888 Mao, 2020, Chem. Sci., 11, 4939, 10.1039/D0SC02213F Romero, 2016, Chem. Rev., 116, 10075, 10.1021/acs.chemrev.6b00057 Corrigan, 2016, Chem. Soc. Rev., 45, 6165, 10.1039/C6CS00185H Qin, 2020, Adv. Synth. Catal., 362, 5093, 10.1002/adsc.202000716 Duan, 2021, Green Chem., 23, 8916, 10.1039/D1GC03060D Zhuang, 2020, ACS Sustain. Chem. Eng., 8, 11729, 10.1021/acssuschemeng.0c03745 de Souza, 2018, J. Org. Chem., 83, 15077, 10.1021/acs.joc.8b02355 Sambiagio, 2019, Trends in Chemistry, 2, 92, 10.1016/j.trechm.2019.09.003 Bédard, 2018, Science, 361, 1220, 10.1126/science.aat0650 Qin, 2021, Green Chem., 23, 6598, 10.1039/D1GC01937F Duan, 2021, Green Synth. Catal., 2, 237, 10.1016/j.gresc.2021.03.001 Yue, 2020, Angew. Chem. Int. Ed., 59, 5738, 10.1002/anie.201914061 Song, 2019, Org. Biomol. Chem., 17, 181, 10.1039/C8OB02912A