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. Author manuscript; available in PMC: 2010 Sep 1.
Published in final edited form as: J Comb Chem. 2009 Sep–Oct;11(5):900–906. doi: 10.1021/cc9000604

Table 2.

Library Data for Compounds 7{1-12}

graphic file with name nihms-129862-t0012.jpg

compd 7 R1 R2 R3 yield(%)a
7{1} MeO H 4-MeOC6H4 86
7{2} MeO H 3-MeOC6H4 87
7{3} MeO H 2-MeOC6H4 93
7{4} MeO H 3,5-(MeO)2C6H3 63
7{5} MeO H 4-Me2NC6H4 79
7{6} H MeO 4-MeOC6H4 89
7{7} H MeO 2-MeOC6H4 91
7{8} MeO MeO 4-MeOC6H4 83
7{9} MeO MeO 2-MeOC6H4 81
7{10} MeO MeO 3-thiophenyl 79b
7{11} graphic file with name nihms-129862-ig0013.jpg 4-MeOC6H4 63
7{12} graphic file with name nihms-129862-ig0014.jpg 2-MeOC6H4 90
a

Isolated yields after column chromatography. All compounds 7 have been characterized by 1H and 13C NMR spectroscopy.

b

An inseparable mixture was obtained.