• 综述 •
张晓鹏*, 董淑祥, 范学森, 张贵生. 邻氨基苯甲酰胺类化合物的合成[J]. 化学进展, 2017, 29(11): 1351-1356.
Xiaopeng Zhang*, Shuxiang Dong, Xuesen Fan, Guisheng Zhang. Synthesis of o-Aminobenzamide Compounds[J]. Progress in Chemistry, 2017, 29(11): 1351-1356.
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[1] Gurulingappa H, Amador M L, Zhao M, Rudek M A, Hidalgo M, Khan S R. Bioorg. Med. Chem., 2004, 14(9):2213. [2] Labrie P, Maddaford S P, Fortin S, Rakhit S, Kotra L P, Gaudreault R C. J. Med. Chem., 2006, 49(26):7646. [3] Ott G R, Cheng M, Learn K S, Wagner J, Gingrich D E, Lisko J G. J. Med. Chem., 2016, 59(16):7478. [4] Shoji N, Umeyama A, Iuchi A, Saito N, Takemoto T, Nomoto K, Ohizumi Y. J. Nat. Prod., 1988, 51(4):791. [5] Kukar T, Murphy M P, Eriksen J L, Sagi S A, Weggen S, Smith T E, Ladd T, Khan M A, Kache R, Beard J, Dodson M, Merit S, Ozols V V, Anastasiadis P Z, Das P, Fauq A, Koo E H, Golde T E. Nat. Med., 2005, 11(5):545. [6] Narsinghani T, Chaturvedi S C. Bioorg. Med. Chem. Lett., 2006, 16(2):461. [7] Englund E E, Neumann S, Eliseeva E, McCoy J G, Titus S, Zheng W, Southall N, Shin P, Thomas C J, Inglese J, Austin C P, Gershengorn M C, Huang W M. MedChemComm, 2011, 2(10):1016. [8] Joubert J, van Dyk S, Green I R, Malan S F. Bioorg. Med. Chem., 2011, 19(13):3935. [9] van Straten N C R, Schoonus Gerritsma G G, van Someren R G, Draaijer J, Adang A E P, Timmers C M, Hanssen R G J M, van Boeckel C A A. ChemBioChem, 2002, 3(10):1023. [10] Verma A, Giridhar R, Kanhed A, Sinha A, Modh P, Yadav M R. ACS Med. Chem. Lett., 2015, 6(2):226. [11] Roy K, De A U, Sengupta C. Drug Des. Discovery, 2002, 18(1):23. [12] Zhang X L, Liu A L, Zhao Y, Xiong L X, Li Z M. Chem. Res. Chin. Univ., 2013, 29(6):1134. [13] Xu Z H, Zhang Y P, Fu H C, Zhong H M, Hong K, Zhu W M. Bioorg. Med. Chem. Lett., 2011, 21(13):4005. [14] Bilokin Y V, Kovalenko S M. Heterocycl. Commun., 2000, 6(5):409. [15] Tian X H, Song L N, Li E T, Wang Q, Yu W Q, Chang J B. RSC Adv., 2015, 5(76):62194. [16] Miyata T, Mizuno T, Nagahama Y, Nishiguchi I, Hirashima T, Sonoda N. Heteroat. Chem., 1991, 2(4):473. [17] Kokten S, Celik I. Synthesis, 2013, 45(18):2551. [18] Li L C, Ren J, Liao T G, Jiang J X, Zhu H J. Eur. J. Org. Chem., 2007, 2007(6):1026. [19] Rai A, Yadav L D S. Eur. J. Org. Chem., 2013, 2013(10):1889. [20] Munegumi T, Kimura E, Sodeyama A, Sakurai A. Asian J. Chem., 2008, 20(4):3079. [21] Campbell J A, McDougald G, McNab H, Rees L V C, Tyas R G. Synthesis, 2007, 20:3179. [22] Fernandez Forner D, Eritja R, Bardella F, Ruiz Perez C, Solans X, Giralt E, Pedroso E. Tetrahedron, 1991, 47(42):8917. [23] Ferrand G, Dumas H, Depin J C, Chavernac G. Eur. J. Med. Chem., 1987, 22(4):337. [24] Wang Z W, Wang M X, Yao X, Li Y, Tan J, Wang L Z, Qiao W T, Geng Y Q, Liu Y X, Wang Q M. Eur. J. Med. Chem., 2012, 53:275. [25] Ozaki K, Yamada Y, Oine T. J. Org. Chem., 1981, 46(8):1571. [26] Yee Y K, Tebbe A L, Linebarger J H, Beight D W, Craft T J, Giffordmoore D S, Goodson T, Herron D K, Klimkowski V J, Kyle J A. J. Med. Chem., 2000, 43(5):873. [27] Xia Z M, Wang K, Zheng J N, Ma Z Y, Jiang Z G, Wang X X, Lv X. Org. Biomol. Chem., 2012, 10(8):1602. [28] Humphrey J M, Chamberlin A R. Chem. Rev., 1997, 28(52):2243. [29] Sheehan J C, Hess G P. J. Am. Chem. Soc., 1955, 77(4):1067. [30] Castro B, Dormoy J R, Evin G, Selve C. Tetrahedron Lett., 1975, 16(14):1219. [31] Carpino L A. J. Am. Chem. Soc., 1993, 115(10):4397. [32] Peet N P, Sunder S, Barbuch R J. J. Heterocycl. Chem., 1980, 17:1513. [33] Rice K D, Aay N, Anand N K, Blazey C M, Bowles O J, Bussenius J, Costanzo S, Curtis J K, Defina S C, Dubenko L, Engst S, Joshi A A, Kennedy A R, Kim A I, Koltun E S, Lougheed J C, Manalo J C L, Martini J F, Nuss J M, Peto C J, Tsang T H, Yu P W, Johnston S. ACS Med. Chem. Lett., 2012, 3(5):416. [34] Mahiwal K, Kumar P, Narasimhan B. Med. Chem. Res., 2012, 21(3):293. [35] Correa A, Tellitu I, Dominguez E, Sanmartin R. J. Org. Chem., 2006, 71(9):3501. [36] Coppola G M M, Ruth I. J. Heterocycl. Chem., 1978, 15(7):1169. [37] Sawatzky E, Wehle S, Kling B, Wendrich J, Bringmann G, Sotriffer C A, Heilmann J, Decker M. J. Med. Chem., 2016, 59(5):2067. [38] Clark P G, Lein M, Keyzers R A. Org. Biomol. Chem., 2012, 10(9):1725. [39] Jourdan F. Eur. J. Inorg. Chem., 1885, 18(1):1444. [40] Ullmann F. Eur. J. Inorg. Chem., 1903, 36(2):2382. [41] Goldberg I. Eur. J. Inorg. Chem., 1906, 39(2):1691. [42] Guram A S, Buchwald S L. J. Am. Chem. Soc., 1994, 116(17):7901. [43] Paul F, Patt J, Hartwig J F. J. Am. Chem. Soc., 1994, 116(13):5969. [44] 王晔峰(Wang Y F), 曾京辉(Zeng J H), 崔晓瑞(Cui X R). 有机化学(Chinese Journal of Organic Chemistry), 2010, 30(2):181. [45] Culf A S, Cuperlovic Culf M, Ouellette R J, Decken A. Org. Lett., 2015, 17(11):2744. [46] Pakrashi S C, Chakravarty A K. J. Org. Chem., 1972, 37(20):3143. [47] Lee D, Kim Y, Chang S. J. Org. Chem., 2013, 78(21):11102. [48] Zhang T, Hu X J, Wang Z, Yang T T, Sun H, Li G G, Lu H J. Chem. Eur. J., 2016, 22(9):2920. [49] Ryu J, Shin K, Park S H, Kim J Y, Chang S. Angew. Chem. Int. Ed., 2012, 51(39):9904. [50] Shin K, Baek Y, Chang S. Angew. Chem. Int. Ed., 2013, 52(31):8031. [51] Figg T M, Park S, Park J, Chang S, Musaev D G. Organometallics, 2014, 33(15):4076. [52] Kim H, Shin K, Chang S. J. Am. Chem. Soc., 2014, 136(16):5904. [53] Kim H, Chang S. ACS Catal., 2015, 5(11):6665. [54] Tran N T T, Tran Q H, Truong T. J. Catal., 2014, 320:9. [55] Yan Q Q, Chen Z K, Yu W L, Yin H, Liu Z X, Zhang Y H. Org. Lett., 2015, 17(10):2482. [56] Zhang L B, Zhang S K, Wei D, Zhu X, Hao X Q, Su J H, Niu J L, Song M P. Org. Lett., 2016, 18(6):1318. [57] Shang M, Sun S Z, Dai H X, Yu J Q. J. Am. Chem. Soc., 2014, 136(9):3354. [58] Tezuka N, Shimojo K, Hirano K, Komagawa S, Yoshida K, Wang C, Miyamoto K, Saito T, Takita R, Uchiyama M. J. Am. Chem. Soc., 2016, 138(29):9166. [59] Yoshida H, Shirakawa E, Honda Y, Hiyama T. Angew. Chem. Int. Ed., 2002, 41(17):3247. [60] Li R, Tang H R, Fu H X, Ren H L, Wang X M, Wu C R, Wu C, Shi F. J. Org. Chem., 2014, 79(3):1344. [61] Guan Z, Nieger M, Schmidt A. Eur. J. Org. Chem., 2015, 2015(21):4710. [62] Katritzky A R, Fan W Q, Akutagawa K. Tetrahedron, 1986, 42(14):4027. [63] Zhang X P, Dong S X, Niu X L, Li Z W, Fan X S, Zhang G S. Org. Lett., 2016, 18(18):4634. |
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