Bertozzi, 2001, Science, 291, 2357, 10.1126/science.1059820
Morenem, 1994, Glycobiology, 4, 113, 10.1093/glycob/4.2.113
Albein, 1987, Annu. Rev. Biochem., 56, 497, 10.1146/annurev.bi.56.070187.002433
Dwek, 1996, Chem. Rev., 96, 683, 10.1021/cr940283b
Branza-Nichita, 2000, Chem. Rev., 100, 4697, 10.1021/cr990291y
Hughs, 1994, Nat. Prod. Rep., 35
Jacobs, 1995, Curr. Opin. Struct. Biol., 5, 605, 10.1016/0959-440X(95)80051-4
Chiba, S. Handbook of Amylases and Related Enzymes, Amylase Research Society of Japan, Ed.; Pergamon: Oxford, 1988; pp 104–116.
Frandesn, 1998, Plant Mol. Biol., 37, 1, 10.1023/A:1005925819741
Braun, 1995, J. Biol. Chem., 270, 26778, 10.1074/jbc.270.45.26778
Dwek, 2002, Nat. Rev. Drug. Discov., 1, 65, 10.1038/nrd708
Robinson, 1991, Diabetes, 40, 825, 10.2337/diabetes.40.7.825
Mehta, 1998, FEBS Lett., 430, 17, 10.1016/S0014-5793(98)00525-0
De Praeter, 2000, Am. J. Hum. Genet., 66, 1744, 10.1086/302948
Fernandes, 1991, Cancer Res., 51, 718
Grzegorzewski, 1989, Cancer Commun., 1, 373, 10.3727/095535489820875066
Humphries, 1986, Cancer Res., 46, 5215
Kato, 2005, J. Med. Chem., 48, 2036, 10.1021/jm0495881
Moreno-Vargas, 2002, Bioorg. Med. Chem. Lett., 12, 2335, 10.1016/S0960-894X(02)00397-9
Heightman, 1999, Angew. Chem. Int. Ed., 38, 750, 10.1002/(SICI)1521-3773(19990315)38:6<750::AID-ANIE750>3.0.CO;2-6
Schaller, 1999, Bioorg. Med. Chem. Lett., 9, 277, 10.1016/S0960-894X(98)00722-7
Chen, 2003, Chem. Rev., 103, 1955, 10.1021/cr0102260
Star, 1971, Phytochemistry, 10, 2812, 10.1016/S0031-9422(00)97288-1
Stevens, 2000, Phytochemistry, 53, 759, 10.1016/S0031-9422(00)00005-4
Nielsen, 1998, J. Med. Chem., 41, 4819, 10.1021/jm980410m
Li, 1995, J. Med. Chem., 38, 5031, 10.1021/jm00026a010
Liu, 2001, J. Med. Chem., 44, 4443, 10.1021/jm0101747
Hsieh, 1998, Pharm. Res., 15, 39, 10.1023/A:1011940401754
Babu, 2003, Bioorg. Med. Chem., 10, 4035, 10.1016/S0968-0896(02)00313-9
Barfod, 2002, Int. Immunopharmacol., 2, 545, 10.1016/S1567-5769(01)00202-8
Rojas, 2002, Bioorg. Med. Chem. Lett., 12, 1951, 10.1016/S0960-894X(02)00317-7
Kumar, 2003, J. Med. Chem., 46, 2813, 10.1021/jm030213+
Ducki, 1998, Bioorg. Med. Chem. Lett., 8, 1051, 10.1016/S0960-894X(98)00162-0
Artico, 1998, J. Med. Chem., 41, 3984, 10.1021/jm9707232
Dhar, 1958, J. Org. Chem., 23, 1159, 10.1021/jo01102a021
Wattanasin, 1980, Synthesis, 8, 647, 10.1055/s-1980-29155
Davey, 1958, J. Chem. Soc., 1230, 10.1039/jr9580001230
Lyle, 1955, J. Am. Chem. Soc., 77, 6667, 10.1021/ja01629a094
Scognamiglio, 2002, Diabetes, 51, 808, 10.2337/diabetes.51.3.808
Selected spectroscopic data 17: mp 183–184°C; 1H NMR (300MHz, δ) 2.35 (3H, s), 6.86 (2H, dd, J=6.8, 1.9Hz), 7.29 (2H, d, J=8.3Hz), 7.37 (3H, m), 7.58 (2H, m), and 7.69 (5H, m).
18: mp 189–190°C; 1H NMR (300MHz, δ) 2.35 (3H, s), 6.85 (1H, d, J=8.2Hz), 7.07 (1H, dd, J=8.3, 2.0Hz), 7.18 (1H, d, J=2.0Hz), 7.27–7.39 (5H, m), 7.62 (1H, d, J=15.6Hz), and 7.68 (4H, m).
19: mp 105–107°C; 1H NMR (300MHz, δ) 2.25 (3H, s), 6.82 (2H, d, J=8.6Hz), 7.23 (4H, m), 7.42 (1H, d, J=15.5Hz), 7.51 (2H, d, J=8.6Hz), 7.66 (1H, d, J=15.5Hz), 7.73 (2H, d, J=8.3Hz), and 7.90 (2H, dd, J=8.7, 2.0Hz).
20: mp 179–180°C; 1H NMR (300MHz, δ) 2.29 (3H, s), 6.78 (1H, d, J=8.2Hz), 6.94 (1H, dd, J=8.2, 2.0Hz), 7.10 (1H, d, J=2.0Hz), 7.19 (5H, m), 7.50 (1H, d, J=15.2Hz), 7.66 (2H, d, J=8.2Hz), and 7.76 (2H, d, J=8.6Hz).
