| [1] Umezawa S, Tatsuta K, Izawa O, et al. A new microbial metabolite phosphoramidon (isolation and structure)[J]. Tetrahedron Lett, 1972, 1: 97－100.[2] Weaver L H, Kester W R, Matthews B W. A crystallographic study of the complex of phosphoramidon with thermolysin. A model for the presumed catalytic transition state and for the binding of extended substrates[J]. J Mol Biol, 1977, 114: 119－132.[3] Kitagishi K, Hiromi K. Binding between thermolysin and its specific inhibitor, phosphoramidon[J]. J Biochem, 1984, 95: 529－534.[4] Kukkola P J, Savage P, Sakane Y J, et al. Differential structure-activity relationships of phosphoramidon analogs for inhibition of 3 metalloproteases: Endothelin-converting enzyme, neutral endopeptidase, and angiotensin-converting enzyme[J]. Cardiovasc Pharmacol, 1995, 26: S65－68.[5] Turner A J. Neuropeptides and Their Peptidases[M]. Chichester, Sussex: Ellis Horwood, 1987. 183－201.[6] De Nanteuil G, Benoist A, Remond G, et al. Synthesis of the endothelin coverting enzyme inhihitor phosphoramidon[J]. Tetrahedron Lett, 1995, 36: 1 435–1 438.[7] Sun Q, Yang Q, Gong S, et al. Synthesis and enzymatic evaluation of phosphoramidon and its β anomer: Anomerzation of α-L-rhamnose triacetate upon phosphitylation[J]. Bioorg Med Chem, 2013, 21: 6 778－6 787.[8] Kang Li-ping(康利平), Wang Yong-ze(王永泽), Feng Bing(冯冰), et al. An NMR study on two glucosylated steroidal saponins of Tb(皂苷Tb 2 个糖基化产物的NMR 研究)[J]. Chinese J Magn Reson(波谱学杂志), 2012, 29 (1): 101－111.[9] Yang Er-bing(杨二冰), Ma Li-bo(马利波), Wang Jin-hui(王金辉), et al. NMR signal assignment and solvent effects of N-substituted indoles(吲哚衍生物NMR 数据归属及其溶剂研究)[J]. Chinese J Magn Reson(波谱学杂志), 2013, 30 (2): 256－263.[10] Sun Q, Xiao Q, Ju Y, et al. Convenient and efficient synthesis of L-rhamnopyranosyl phosphoramidates via H-phosphonate[J]. Chinese Chem Lett, 2003, 14: 685－688.[11] Donahue M G, Johnston J N. Preparation of a protected phosphoramidon precusor via an H-phosphonate coupling strategy[J]. Bioorg Med Chem Lett, 2006, 16: 5 602－5 604.[12] Duus J O, Gotfredsen C H, Bock K. Carbohydrate structural determination by NMR spectroscopy: modern methods and limitations[J]. Chem Rev, 2000, 100: 4 589－4 614.[13] Uhrinova S, Uhrin D, Liptaj T, et al. NMR of carbohydrates 1D homo nuclear selective methods[J]. Magn Reson Chem, 1991, 29: 912－922.[14] Pedersen A T, Anderson O M, Aksnes D W, et al. Anomeric sugar configuration of anthocyanin O-pyranosides determinded from heteronuclear one-bond coupling contants[J]. Phytochem Analysis, 1995, 6: 313－316. |
