1Pierre Fabre. Forest and cypress announce FDA approval of Savella(^TM) for the management of fibromyalgia[ EB/OL]. [2009 -06 -30]. http ://frx. com/ ID = 1244788. aspx?.
2SHUTO S, ONO S, HASE Y, et al. Synthesis of( + )- and ( - )-milnaciprans and their conformationally restricted analogs[ J ]. Tetrahedron Lett, 1996,37 (5) :641 - 644.
3BONNAUD B, COUSSE H, MOUZIN G, et al. 1-Aryl-2- (aminomethyl) cyclopropane carboxylic acid derivatives. A new series of potential antidepressant[ J]. J Med Chem, 1987, 30(2) :318 -325.
1Viazzo P, Alphand V, Furstoss R.Enantioselective hydrolysis of a key-lactone involved in the synthesis of the antidepressant milnacipran [J].Tetrahedron Lett, 1996, 37 (26): 4519-4522.
2Shuto S, Ono S, Hase Y, et al.Synthesis of (+) - and (-)milnacipran and their conformationally restricted analogs [J].Tetrahedron Lett, 1996, 37 (5): 641-644.
3Bonnaud B, Cousse H, Mouzin G, et al.1-Aryl-2-(aminomethyl) cyclopropane carboxylic acid derivatives.A new series of potential antidepressant [J].J Med Chem,1987, 30(2): 318-325.
4Shuto S, Ono S, Hase Y, et al.Conformational restriction by repulsion between adjacent substituents on a cyclopropane ring: design and enantioselective synthesis of 1-phenyl-2-(1-aminoalkyl)-N,N-diethylcyclopropane carboxamides as potent NMDA receptor ant
5BNNAUD B,COUSSE H,MOUZIN G,et al. 1-Aryl-2- (aminomethyl) Cyclopropane Carboxylic Acid Deriva- tives. A New Series of Potential Antidepressant[J]. JMed Chem, 1987,30(2) :318-325.
6ANSSEAU M, YON FRENCKEU R, MERTENS C, et al. Controlled Comparison of Two Doses of Milnacipran (F2207) and Ami-triptyline in Major Depressiveinpatients[J]. Psychopharmaeol ogy ( Berl ), 1989,98 ( 2 ) : 163-168.
7VIAZZO P,ALPHAND V, FURSTOSS R. Enantiose lective Hydrolysis of a Key-lactone Involved in the Synthesis of the Antidepressant Milnacipran[J]. Tetrahedron Lett,1996,37(26) : 4519-4522.
8SHUTO S,ONO S, HASE Y,et al. Synthesis of (+) and (--) Milnacipran and Their Conformationally Re- stricted Analogs [J ]. Tetrahedron Lett, 1996,37 ( 5 ) : 641-644.
9SHUTO S, ONO S, HASE Y, et al. Conformational Restriction by Repulsion Between Adjacent Substituents on a Cyclopropane Ring: design and Enantioselecrive Synthesis of 1-phenyl-2-(1-aminoalkyl)-N, N-di- ethylcyclopropane Carboxamides as Potent NMDA Receptor Antagonists[J]. J Org Chem, 1996,61 (3) : 916- 923.
