[1] Quezada E, Delogu G, Picciau C, et al. Synthesis and vasorelaxant and platelet antiaggregatory activities of a new series of 6-halo-3-phenylcoumarins[J]. Molecule, 2010, 15(1): 270―279.[2] Anand P, Singh B, Singh N. A review on coumarins as acetylcholinesterase inhibitors for Alzheimer's disease[J]. Bioorg Med Chem, 2012, 20(3): 1 175―1 180.[3] Spino C, Dodier M, Sotheeswaran S. Anti-HIV coumarins from Calophyllum seed oil[J]. Bioorg Med Chem Lett, 1998, 8(24): 3 475―3 478.[4] Budzisz E, Brzezinska E, Krajewska U, et al. Cytotoxic effects, alkylating properties and molecular modeling of coumarin derivatives and their phosphonic analogues[J]. Eur J Med Chem, 2003, 38(6): 597―603.[5] Robison C N, Addison J F. Condensation of trethyl phosphonoacetate with aromatic aldehydes[J]. J Org Chem, 1966, 31(12): 4 325―4 326.[6] Bouyssou P, Chenault J. Phosphonates and phosphine oxides as reagents in a one-pot synthesis of coumarins[J]. Tetrahedron Lett, 1991, 32(39): 5 341―5 344.[7] Zhou P, Jiang Y J, Zou J P, et al. Manganese(III) acetate mediated free radical phosphonylation of flavones and coumarins[J]. Synthesis, 2012, 44(7): 1 043―1 050.[8] Mi X, Huang M M, Zhang J Y, et al. Regioselective palladium-catalyzed phosphonation of coumarins with dialkyl H-phosphonates via C-H functionalization[J]. Org Lett, 2013, 15(24): 6 266―6 269.[9] Mi X, Wang C Y, Huang M M, et al. Silver-catalyzed synthesis of 3-phosphorated coumarins via radical cyclization of alkynoates and dialkyl H-phosphonates[J]. Org Lett, 2014, 16(12): 3 356―3 359.[10] Zhou Z Z, Jin D P, Li L H, et al. Silver-promoted oxidative cyclization of 1, 6-enynes: Highly regioselective synthesis of phosphorated fluorine derivatives[J]. Org Lett, 2014, 16(21): 5 616―5 619.[11] Wei W, Ji J X. Catalytic and direct oxyphosphorylation of alkenes with dioxygen and H-phosphonates leading to β-ketophosphonates[J]. Angew Chem Int Ed, 2011, 50(39): 9 097―9 099.[12] Li, Y M, Sun, M, Wang, H L, et al. Direct annulations toward phosphorylated oxindoles by silver-catalyzed carbon- phosphorus functionalization of alkenes[J]. Angew Chem, Int Ed, 2013, 52(14): 3 972―3 976.[13] Mi, X, Wang, C Y, Huang, M M, et al. Silver-catalyzed carbonphosphonation of α, α-diaryl allylic alcohols: sythesis of β-aryl-γ-ketophosphonates[J]. Org Biomol Chem, 2014, 42(12): 8 394―8 397.[14] Chen Xiao-lan(陈晓岚), Xu Shao-hua(徐少华), Qu Ling-bo(屈凌波), et al. Spectroscopic characterization of 6-nitryl-7-diisopropyl coumarin phosphate(6-硝基-7-二异丙基香豆素磷酸酯的结构确定)[J]. Chinese J Magn Reson(波谱学杂志), 2010, 27(4): 635―641.[15] Zhao Tian-zeng(赵天增). Proton NMR Spectroscopy(核磁共振氢谱)[M]. Beijing(北京): Peking University Press(北京大学出版社), 1983, 107―173.[16] Ning Yong-cheng(宁永成). Structural Identification of Organic Compounds and Organic Spectroscopy(有机化合物结构鉴定与有机波谱学)[M]. Beijing(北京): Science Press(科学出版社), 2000. |