Guo Ruiyun, Chang Junbiao, Chen Rongfeng, Fan Xiaoling , Xie Jingxi, . THANSFORMING THE CARBOMETHOXY OF α-DIMETHYL DICARBOXYLATE BIPHENYLJ. Acta Pharmaceutica Sinica, 1999, 34(6): 439-441.
Citation: Guo Ruiyun, Chang Junbiao, Chen Rongfeng, Fan Xiaoling , Xie Jingxi, . THANSFORMING THE CARBOMETHOXY OF α-DIMETHYL DICARBOXYLATE BIPHENYLJ. Acta Pharmaceutica Sinica, 1999, 34(6): 439-441.

THANSFORMING THE CARBOMETHOXY OF α-DIMETHYL DICARBOXYLATE BIPHENYL

  • AIM: To synthesize some new analogues of α-DDB (dimethyl 4,4′-dimethoxy-5,6,5′,6′-dimethylenedioxy-2,2′-biphenyl dicarboxylate). METHODS: Structure modification to the carbomethoxy of α-DDB to synthesize some symmetrical and asymmetrical biphenyl anlogues. The structures of these compounds are confirmed by IR, 1HNMR, MS and EA. RESULTS: Nine dirivatives of α-DDB have been synthesized and three of them (3, 4 and 5) are new compounds. CONCLUSION: Most of these compounds have antitumor activities.
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