Diverse synthesis of the C ring fragment of bryostatins via Zn/Cu-promoted conjugate addition of α-hydroxy iodide with enone
Tài liệu tham khảo
Hale, 2010, Chem. Asian J., 5, 704, 10.1002/asia.200900634
Tian, 2018, Future Med. Chem., 10, 1497, 10.4155/fmc-2018-0012
Wu, 2020, Chem. Eur. J., 26, 1166, 10.1002/chem.201903128
Raghuvanshi, 2020, Curr. Top. Med. Chem., 20, 1124, 10.2174/1568026620666200325110444
Pettit, 1982, J. Am. Chem. Soc., 104, 6846, 10.1021/ja00388a092
Farlow, 2019, J. Alzheimers Dis., 67, 555, 10.3233/JAD-180759
Wang, 2019, Biochem. Biophys. Res. Commun., 512, 473, 10.1016/j.bbrc.2019.03.014
Way, 2001, Diabet. Med., 18, 945, 10.1046/j.0742-3071.2001.00638.x
Mizutani, 2016, Neuroreport., 27, 659, 10.1097/WNR.0000000000000592
Nelson, 2017, J. Alzheimer’s Dis., 58, 521, 10.3233/JAD-170161
Sarajärvi, 2018, Neuropharmacology, 141, 76, 10.1016/j.neuropharm.2018.08.020
Murakami, 2020, Int. J. Mol. Sci., 21, 1179, 10.3390/ijms21041179
Marsden, 2017, PLoS Pathog., 13, 10.1371/journal.ppat.1006575
Zhao, 2019, Pharmacol. Res., 139, 524, 10.1016/j.phrs.2018.10.023
Heffern, 2019, J. Virus Erad., 5, 84, 10.1016/S2055-6640(20)30057-1
Proust, 2020, J. Glia, 68, 2212, 10.1002/glia.23833
Li, 2020, Sci. Rep., 10, 3511, 10.1038/s41598-020-60614-1
Ketcham, 2016, J. Am. Chem. Soc., 138, 13415, 10.1021/jacs.6b08695
Trost, 2007, J. Am. Chem. Soc., 129, 2206, 10.1021/ja067305j
Kedei, 2015, J. Nat. Prod., 78, 896, 10.1021/acs.jnatprod.5b00094
Staveness, 2016, J. Nat. Prod., 79, 680, 10.1021/acs.jnatprod.5b01017
Baumann, 2016, J. Org. Chem., 81, 7862, 10.1021/acs.joc.6b01516
Mears, 2019, Org. Biomol. Chem., 17, 1487, 10.1039/C8OB03152E
Kraft, 2014, J. Am. Chem. Soc., 136, 13202, 10.1021/ja5078188
Andrews, 2014, J. Am. Chem. Soc., 136, 13209, 10.1021/ja507825s
Sloane, 2020, Proc. Natl. Acad. Sci. U. S. A., 117, 10688, 10.1073/pnas.1919408117
Hardman, 2020, Nat. Commun., 11, 1879, 10.1038/s41467-020-15742-7
Keck, 2011, J. Am. Chem. Soc., 133, 744, 10.1021/ja110198y
Wender, 2017, Science, 358, 218, 10.1126/science.aan7969
Evans, 1998, Angew. Chem. Int. Ed., 37, 2354, 10.1002/(SICI)1521-3773(19980918)37:17<2354::AID-ANIE2354>3.0.CO;2-9
Evans, 1999, J. Am. Chem. Soc., 121, 7540, 10.1021/ja990860j
Ohmori, 2000, Angew. Chem. Int. Ed., 39, 2290, 10.1002/1521-3773(20000703)39:13<2290::AID-ANIE2290>3.0.CO;2-6
Trost, 2020, Science, 368, 1007, 10.1126/science.abb7271
Kageyama, 1990, J. Am. Chem. Soc., 112, 7407, 10.1021/ja00176a058
Lu, 2011, J. Am. Chem. Soc., 133, 13876, 10.1021/ja205673e
Manaviazar, 2006, Org. Lett., 8, 4477, 10.1021/ol061626i
Zhang, 2018, Angew. Chem. Int. Ed., 57, 942, 10.1002/anie.201711452
Wender, 2011, J. Am. Chem. Soc., 133, 9228, 10.1021/ja203034k
Trost, 2008, Nature, 456, 485, 10.1038/nature07543
Trost, 2010, J. Am. Chem. Soc., 132, 16403, 10.1021/ja105129p
Knochel, 1993, Chem. Rev., 93, 2117, 10.1021/cr00022a008
Alexakis, 2008, Chem. Rev., 108, 2796, 10.1021/cr0683515
Zhou, 2018, Org. Chem. Front., 5, 3579, 10.1039/C8QO01141A
Shin, 2019, J. Org. Chem., 84, 4558, 10.1021/acs.joc.9b00369
Ouyang, 2019, Tetrahedron, 75, 4486, 10.1016/j.tet.2019.06.034
Krasovskiy, 2010, Org. Lett., 12, 4742, 10.1021/ol101885t
Duplais, 2011, Organometallics, 30, 6090, 10.1021/om200846h
Lipshutz, 2011, J. Org. Chem., 76, 5061, 10.1021/jo200746y
Lipshutz, 2012, J. Am. Chem. Soc., 134, 19985, 10.1021/ja309409e
Pang, 2019, J. Am. Chem. Soc., 141, 17117, 10.1021/jacs.9b04510
Petrier, 1986, Tetrahedron Lett., 27, 3149, 10.1016/S0040-4039(00)84739-5
Luche, 1988, Tetrahedron Lett., 29, 5369, 10.1016/S0040-4039(00)82870-1
Luche, 1988, Tetrahedron Lett., 29, 5373, 10.1016/S0040-4039(00)82871-3
Dupuy, 1991, Synth. Commun., 21, 643, 10.1080/00397919108020831
Sarandeses, 1992, Soc. Chem. Commun., 11, 798, 10.1039/C39920000798
Li, 2005, Chem. Rev., 105, 3095, 10.1021/cr030009u
Li, 2006, Chem. Soc. Rev., 35, 68, 10.1039/B507207G
Kim, 2020, Green. Synth. Catal., 1, 1, 10.1016/j.gresc.2020.06.002
Yadav, 2005, Tetrahedron Lett., 46, 2133, 10.1016/j.tetlet.2005.01.121
Baldwin, 1977, J. Org. Chem., 42, 3846, 10.1021/jo00444a011