Multicomponent cascade reaction of 3-formylchromones: Highly regioselective synthesis of functionalized pyridin-2(1H)-ones

Green Synthesis and Catalysis - Tập 4 - Trang 231-239 - 2023
Xinghan Yun1, Li Chen1, Ying Lv1, Zihan Lu1, Kun Huang1, Shengjiao Yan1
1Key Laboratory of Medicinal Chemistry for Natural Resource (Yunnan University), Ministry of Education, School of Chemical Science and Technology, Yunnan University, Kunming 650091, China

Tài liệu tham khảo

Zhu, 2005 Ganem, 2009, Acc. Chem. Res., 42, 463, 10.1021/ar800214s D ömling, 2006, Chem. Rev., 106, 17, 10.1021/cr0505728 Kong, 2020, Green Chem., 22, 256, 10.1039/C9GC03692J Zhang, 2017, ACS Sustain. Chem. Eng., 5, 6175, 10.1021/acssuschemeng.7b01102 Hao, 2016, J. Org. Chem., 81, 11276, 10.1021/acs.joc.6b02249 Gao, 2016, Chem. Commun., 52, 900, 10.1039/C5CC08071A Maleki, 2015, Org. Prep. Proced. Int., 47, 368, 10.1080/00304948.2015.1066647 Maleki, 2016, Org. Prep. Proced. Int., 48, 37, 10.1080/00304948.2016.1127098 Maleki, 2020, Polycycl. Aromat. Comp., 40, 633, 10.1080/10406638.2018.1469519 Maleki, 2020, Org. Prep. Proced. Int., 52, 328, 10.1080/00304948.2020.1765655 Blake, 2016, J. Med. Chem., 59, 5650, 10.1021/acs.jmedchem.6b00389 Rohde, 2021, J. Med. Chem., 64, 4913, 10.1021/acs.jmedchem.1c00019 Li, 2019, Chem. Commun., 55, 4407, 10.1039/C9CC00917E Wu, 2016, Org. Biomol. Chem., 14, 1413, 10.1039/C5OB02154E Cid, 2014, J. Med. Chem., 57, 6495, 10.1021/jm500496m Hibi, 2012, J. Med. Chem., 55, 10584, 10.1021/jm301268u Wacker, 2014, J. Med. Chem., 57, 7499, 10.1021/jm501175v Mugnaini, 2020, J. Med. Chem., 63, 7369, 10.1021/acs.jmedchem.0c00595 Huang, 2012, Org. Lett., 14, 370, 10.1021/ol203124f Xiang, 2008, Org. Lett., 10, 345, 10.1021/ol702846t Pan, 2007, Org. Lett., 9, 2421, 10.1021/ol070905i Apsunde, 2014, J. Org. Chem., 79, 3260, 10.1021/jo500284n Shintani, 2016, Chem. Sci., 7, 1205, 10.1039/C5SC03767K Yi, 2010, Chem. Commun., 46, 6941, 10.1039/c0cc01815e Nagaraju, 2015, Org. Biomol. Chem., 13, 3011, 10.1039/C4OB01578A Zhang, 2017, Green Chem., 19, 919, 10.1039/C6GC03355E Krishnamurti, 2018, Chem. Commun., 54, 10574, 10.1039/C8CC04907F Kumar, 2017, Org. Biomol. Chem., 15, 5457, 10.1039/C7OB01277B Hu, 2018, Org. Biomol. Chem., 16, 4151, 10.1039/C8OB00860D Wen, 2012, Green Chem., 14, 707, 10.1039/c2gc16388h Haas, 1981, J. Heterocycl. Chem., 18, 607, 10.1002/jhet.5570180334 Ahadi, 2021, J. Org. Chem., 86, 12705, 10.1021/acs.joc.1c01220 Seixas, 2016, ChemistrySelect, 1, 318, 10.1002/slct.201600080 Sengupta, 2012, Chem. Eur. J., 18, 1905, 10.1002/chem.201103354 Medina, 2015, Nat. Prod. Rep., 32, 1472, 10.1039/C4NP00162A Reis, 2017, J. Med. Chem., 60, 7941, 10.1021/acs.jmedchem.6b01720 Cai, 2016, Chem. Commun., 52, 7661, 10.1039/C6CC02381A Fan, 2021, Org. Chem. Front., 8, 4508, 10.1039/D1QO00666E Chen, 2017, ACS Sustain. Chem. Eng., 5, 1899, 10.1021/acssuschemeng.6b02622 Muhammad, 2012, Synlett, 23, 1755, 10.1055/s-0031-1289787 Poomathi, 2017, Green Chem., 19, 2524, 10.1039/C6GC03440C Fan, 2017, Org. Lett., 19, 5984, 10.1021/acs.orglett.7b03007 Lepitre, 2017, Org. Lett., 19, 1978, 10.1021/acs.orglett.7b00309 Liao, 2017, Chem. Commun., 53, 9067, 10.1039/C7CC03468G Chen, 2020, Green Chem., 22, 6943, 10.1039/D0GC02460K Chen, 2021, Chem. Commun., 57, 7657, 10.1039/D1CC02437J Wu, 2020, Natl. Sci. Rev., 7, 588, 10.1093/nsr/nwz203 Wu, 2021, Chem. Eur. J., 27, 8013, 10.1002/chem.202100700 Jin, 2022, Front. Chem., 10, 860398, 10.3389/fchem.2022.860398