Electrochemical synthesis of euglobal-G1, -G2, -G3, -G4, -T1 and -IIc

Electrochemical synthesis of euglobal-G1, -G2, -G3, -G4, -T1 and -IIc
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DOI:
10.1039/a802306i
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发表时间:
1998-09-07
期刊:
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
影响因子:
--
通讯作者:
Tada, M
Tada, M
中科院分区:
其他
文献类型:
--
作者:
Chiba, K;Arakawa, T;Tada, M

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用电化学方法合成了六种天然优球蛋白。在关键步骤中,以2,3-二氯-5,6-二氰基对苯二酚(DDQH(2))为氧化还原介质,原位生成的醌类化合物与萜烯类化合物在PTFE纤维涂层电极表面进行环加成反应,生成天然产物。
Six natural euglobals were synthesized by electrochemical methods. In a key step, cycloaddition between in situ generated quinomethanes and terpenes was performed on the surface of PTFE-fibre coated electrode to give natural products using 2,3-dichloro-5,6-dicyano-p-hydroquinone (DDQH(2)) as a redox mediator, In this reaction system, biomimetic generation and cycloaddition of the unstable quinomethanes were efficiently completed by the selective oxidation of cresol derivatives.