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Synthesis of Boswellic Acid Derivatives and Primary Research on their Activities 被引量:2
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作者 YanQiuMENG LinXiangZHAO +2 位作者 ZanWANG DanLIU YongKuiJING 《Chinese Chemical Letters》 SCIE CAS CSCD 2005年第7期867-870,共4页
In order to search for new potent anti-cancer agents, a series of boswellic acid derivatives were designed and synthesized. Six of them were identified by IR, NMR and MS as new compounds and biologic assay of anti-can... In order to search for new potent anti-cancer agents, a series of boswellic acid derivatives were designed and synthesized. Six of them were identified by IR, NMR and MS as new compounds and biologic assay of anti-cancer is underway. 展开更多
关键词 Boswellic acid design synthesis.
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Syntheses of Tetrahydropyrrolizino[2,1-c]quinoline Derivatives 被引量:1
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作者 SONGHong-rui WANGFei LIJian ZHANGShou-fang 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2005年第4期460-462,共3页
The three title compounds were prepared from 2-phenylaminomethyl-3H-1,2-dihydro-1-pyrrolizinols via an intramolecular Friedel-Crafts reaction. 2-Phenylaminomethyl-3H-1,2-dihydro-1-pyrrolizinols were prepared from 2-ph... The three title compounds were prepared from 2-phenylaminomethyl-3H-1,2-dihydro-1-pyrrolizinols via an intramolecular Friedel-Crafts reaction. 2-Phenylaminomethyl-3H-1,2-dihydro-1-pyrrolizinols were prepared from 2-phenylaminomethyl-3H-1,2-dihydro-1-pyrrolizinones via reduction. The heterocyclic ring system of pyrrolizino[2,1-c]quinoline has not been found in literature. 展开更多
关键词 Pyrrolizino[2 1-c]quinoline SYNTHESIS HETEROCYCLES
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Synthesis of N1-Substituted-3-aryl-4-alkyl-4, 5-dihydro-1H-1-pyra-zolethiocarboxamide as Novel Small Molecule Inhibitors of Cysteine Protease of T.cruzi
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作者 ChunGUO XiaoHuiDU 《Chinese Chemical Letters》 SCIE CAS CSCD 2002年第11期1043-1046,共4页
A series of N1-substituted-3-aryl-4-alkyl-4, 5-dihydro-1H-1-pyrazolethiocarboxamide were prepared from the Mannich bases of aryl ketones in good yields. Some derivatives were found to be active against the cysteine p... A series of N1-substituted-3-aryl-4-alkyl-4, 5-dihydro-1H-1-pyrazolethiocarboxamide were prepared from the Mannich bases of aryl ketones in good yields. Some derivatives were found to be active against the cysteine protease of T.cruzi.. 展开更多
关键词 N1-substituted-3-aryl-4-alkyl-4 5-dihydro-1H-1-pyrazolethiocarboxamide synthesis T.cruzi. cysteine protease inhibitor.
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