Copper- versus palladium-catalyzed aromatization of 2-(methoxycarbonyl) tetralones: synthesis of methyl 1-hydroxy-2-naphthoates

Zhang, 2011, Inflamm. Res., 60, 851, 10.1007/s00011-011-0345-2 Morand, 2003, PCT Int. Appl. Connor, 1992, J. Med. Chem., 35, 958, 10.1021/jm00083a023 Sastry, 2010, J. Org. Chem., 75, 2274, 10.1021/jo100024b Meyers, 1981, J. Org. Chem., 46, 3881, 10.1021/jo00332a024 Zjawiony, 1991, Org. Prep. Proced. Int., 23, 163, 10.1080/00304949109458304 Hauser, 1977, J. Org. Chem., 42, 4155, 10.1021/jo00445a041 Franck, 1986, J. Am. Chem. Soc., 108, 2455, 10.1021/ja00269a059 Ozaki, 1996, Chem. Pharm. Bull., 44, 1785, 10.1248/cpb.44.1785 Huang, 2007, J. Org. Chem., 72, 3965, 10.1021/jo070241q Shahzad, 2010, Org. Lett., 12, 1364, 10.1021/ol100274e Youn, 2012, J. Am. Chem. Soc., 134, 11308, 10.1021/ja304616q Banerjee, 2002, Russ. J. Gen. Chem., 73, 1815, 10.1023/B:RUGC.0000018662.02489.8d Cui, 2011, Org. Lett., 13, 6488, 10.1021/ol202777h Hurtley, 1929, J. Chem. Soc., 1870, 10.1039/JR9290001870 Yip, 2007, Org. Lett., 9, 3469, 10.1021/ol701473p For copper-catalyzed arylation reactions, see: Okuro, 1993, J. Org. Chem., 58, 7606, 10.1021/jo00078a053 Hennessy, 2002, Org. Lett., 4, 269, 10.1021/ol017038g Xie, 2005, Org. Lett., 7, 4693, 10.1021/ol0518838 Satoh, 1997, Angew. Chem., Int. Ed., 36, 1740, 10.1002/anie.199717401 Palucki, 1997, J. Am. Chem. Soc., 119, 11108, 10.1021/ja972593s Hamann, 1997, J. Am. Chem. Soc., 119, 12382, 10.1021/ja9727880 Moss, 2008, J. Am. Chem. Soc., 130, 10076, 10.1021/ja8036965 Yin, 2013, Adv. Synth. Catal., 355, 1924, 10.1002/adsc.201300335 For a review, see Christoffers, 2004, Adv. Synth. Catal., 346, 143, 10.1002/adsc.200303140 Smith, 2011, Chem. Rev., 111, 1637, 10.1021/cr100197z Russo, 2012, RSC Adv., 2, 385, 10.1039/C1RA00612F Watanabe, 1999, Tetrahedron Lett., 40, 7795, 10.1016/S0040-4039(99)01618-4 Jiang, 2010, Tetrahedron: Asymmetry, 21, 794, 10.1016/j.tetasy.2010.05.011 See, for instance Ishikawa, 1999, J. Org. Chem., 64, 5691, 10.1021/jo9824854 Yang, T. -F.; Wang, K. -Y.; Li, H. -W.; Tseng, Y. -C.; Lien, T. -C. 2012, 53, 585−588. Xiao, 2013, Org. Lett., 15, 1254, 10.1021/ol400186b Ji, 2014, Org. Biomol. Chem., 12, 8488, 10.1039/C4OB01594K Yin, 2015, Org. Biomol. Chem., 13, 9012, 10.1039/C5OB01203A Simon, 2012, Angew. Chem., Int. Ed., 51, 7537, 10.1002/anie.201200698 Kotnis, 1991, Tetrahedron Lett., 32, 3441, 10.1016/0040-4039(91)80801-C Hirao, 1990, J. Org. Chem., 55, 358, 10.1021/jo00288a065 Moriuchi, 2009, Tetrahedron Lett., 50, 7385, 10.1016/j.tetlet.2009.10.070 See, for instance Horning, 1947, J. Am. Chem. Soc., 69, 1359, 10.1021/ja01198a035 Muzart, 1982, J. Mol. Catal., 15, 373, 10.1016/0304-5102(82)80029-1 Monguchi, 2008, Synlett, 2291 Imahori, 2012, Org. Lett., 14, 1172, 10.1021/ol300145g Sutter, 2013, Green Chem., 15, 347, 10.1039/C2GC36776A Sutter, 2013, Eur. J. Org. Chem., 5902, 10.1002/ejoc.201300485 Izawa, 2013, Angew. Chem., Int. Ed., 52, 3672, 10.1002/anie.201209457 Zhou, 2013, Chem.—Eur. J., 19, 7151, 10.1002/chem.201300491 Izawa, 2011, Science, 333, 209, 10.1126/science.1204183 Diao, 2013, J. Am. Chem. Soc., 135, 8205, 10.1021/ja4031648 Pun, 2013, J. Am. Chem. Soc., 135, 8213, 10.1021/ja403165u For reviews, see Muzart, 2010, Eur. J. Org. Chem., 3779, 10.1002/ejoc.201000278 Campbell, 2012, Acc. Chem. Res., 45, 851, 10.1021/ar2002045 Brown, 1995, Tetrahedron, 51, 3587, 10.1016/0040-4020(95)00075-J Gould, 2011, J. Med. Chem., 54, 1836, 10.1021/jm101479y Hashem, 1976, J. Med. Chem., 19, 229, 10.1021/jm00224a007 Johnson, 1974, Aust. J. Chem., 27, 1277, 10.1071/CH9741277 Yamada, 2001, PCT Int. Appl. Kloetzel, 1940, J. Am. Chem. Soc., 62, 1708, 10.1021/ja01864a020 Solladié-Cavallo, 2001, Tetrahedron: Asymmetry, 12, 2605, 10.1016/S0957-4166(01)00441-4 Chakraborti, 1999, J. Org. Chem., 64, 8014, 10.1021/jo990035l Sugihara, 1988, Eur. Pat. Appl. Hill, 1937, J. Chem. Soc., 937, 10.1039/jr9370000937 Himmele, 1972, Ger. Offen.