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Synthesis and biological evaluation of ethyl 6-alkoxy-7-phenyl-4-hydroxy-3-quinolinecarboxylates against Eimeria tenella 被引量:5
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作者 Zhang, Yuan Yuan Zeng, Xing Yan +3 位作者 Nie, Kui Zhong, Zhi Cheng Wang, Yu Liang Wang, Yu Zhong 《Chinese Chemical Letters》 SCIE CAS CSCD 2010年第4期426-428,共3页
关键词 Ethyl 6-alkoxy-7-phenyl-4-hydroxy-3-quinolinecarboxylate Synthesis Anticoccidial activity Eimeria tenella
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Synthesis of Gingerenone C and 5-Hydroxy-1-(4′-hydroxy-3-methoxyphenyl)-7-(4′′-hydroxyphenyl)-3-heptanone 被引量:2
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作者 Shao Bai LI Yun Gen LIU 《Chinese Chemical Letters》 SCIE CAS CSCD 2003年第3期251-254,共4页
The two diarylheptanoids (E)-1-(4-hydroxy-3-methoxyphenyl)-7-(4-hydroxyphenyl) hept-4-en-3-one 1 (Gingerenone C) and (±)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-7-(4- hydroxyphenyl)-3-heptanone 2 were synthesized... The two diarylheptanoids (E)-1-(4-hydroxy-3-methoxyphenyl)-7-(4-hydroxyphenyl) hept-4-en-3-one 1 (Gingerenone C) and (±)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-7-(4- hydroxyphenyl)-3-heptanone 2 were synthesized from vanillin 3 and 4-hydroxybenzaldehyde 9. 展开更多
关键词 DIARYLHEPTANOIDS (E)-1-(4-hydroxy-3-methoxyphenyl)-7-(4-hydroxyphenyl)hept- 4-en-3-one Gingerenone C (±)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-7-(4-hydroxy- phenyl)-3-heptanone synthesis.
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A Facile Synthesis of 6β-Hydroxy-7α(H)-eudesma-4-en-3-one
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作者 Gang ZHOU Zhao Ming XIONG +1 位作者 Yong Gang CHEN Yu Lin LI (National Laboratory of Applied Organic Chemistry and Institute of Organic Chemistry,Lanzhou University, Lanzhou 730000) 《Chinese Chemical Letters》 SCIE CAS CSCD 1998年第9期817-818,共2页
A stereoselective total synthesis of 6β-hydroxy-7α(H)-eudesma-4-en-3- 1startingfrom (+)-dihydrocarvone 7 has been described.
关键词 synthesis SESQUITERPENE -hydroxy-7α(H)-eudesm-4-en-3-one sihydrocarvone
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A New Chromone Derivative from Stellera chamaejasme L 被引量:6
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作者 Bao Min FENG Yue Hu PEI Hui Ming HUA 《Chinese Chemical Letters》 SCIE CAS CSCD 2002年第8期738-739,共2页
A new chromone derivative, 3-[1- (2, 4, 6-trihydroxyphenyl) 3-di-(4-hydroxyphenyl) 1-propanone-2-yl] 5,7-dihydroxy-8-di(4-hydroxyphenyl)methyl-4H-1-benzopyran-4-one, named as isomohsenone was isolated from the roots o... A new chromone derivative, 3-[1- (2, 4, 6-trihydroxyphenyl) 3-di-(4-hydroxyphenyl) 1-propanone-2-yl] 5,7-dihydroxy-8-di(4-hydroxyphenyl)methyl-4H-1-benzopyran-4-one, named as isomohsenone was isolated from the roots of Stellera chamaejasme L. together with known chamaechromone. Its structure was determined by the analysis of MS and NMR data, especially 2D NMR spectra. 展开更多
关键词 Stellera chamaejasme L. CHROMONE 3-[1- (2 4 6-trihydroxyphenyl) 3-di-(4-hydroxy- phenyl)-1-propanone-2-yl] 5 7-dihydroxy-8-di-(4-hydroxyphenyl) methyl-4H-1- benzopyran-4- one.
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Indole Alkaloids from the Roots of Ervatamia hainanensis 被引量:4
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作者 Jian Peng HUANG Zi Ming FENG +2 位作者 Chong Fei ZHENG Pei Cheng ZHANG Yang Min MA 《Chinese Chemical Letters》 SCIE CAS CSCD 2006年第6期779-782,共4页
Two new indole alkaloids, named ibogamine-18-carboxylic acid, 3, 4-didehydro-7, 8-dioxo-methyl ester 1, ibogamine-18-carboxylic acid, 16, 17-didehydro-9, 17-dihydro-9-hydroxy (2-oxopropyl)-methyl ester 2, were isola... Two new indole alkaloids, named ibogamine-18-carboxylic acid, 3, 4-didehydro-7, 8-dioxo-methyl ester 1, ibogamine-18-carboxylic acid, 16, 17-didehydro-9, 17-dihydro-9-hydroxy (2-oxopropyl)-methyl ester 2, were isolated from Ervatamia hainanensis. Their structures were elucidated on the basis of spectroscopic methods. 展开更多
关键词 Ervatamia hainanensis indole alkaloid ibogamine-18-carboxylic acid 3 4-didehydro-7 8-dioxo-methyl ester ibogamine- 18-carboxylic acid 16 17-didehydro-9 17-dihydro-9-hydroxy-(2-oxopropyl)-methyl ester.
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A New Halogenated Biindole and A New Apo-carotenone from Green Alga Chaetomorpha basiretorsa Setchell 被引量:6
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作者 DaYongSHI LiJunHAN +5 位作者 JieSUN ShuaiLI SuJuanWANG YongChunYANG XiaoFAN JianGongSHI 《Chinese Chemical Letters》 SCIE CAS CSCD 2005年第6期777-780,共4页
关键词 Green alga Chaetomorpha basiretorsa Sethcell 4 4′-dichloro-5 5′-dibromo-7 7′-di- methoxy-2 2′-bi-1H-indole 1′S* 4′R*-8-(4-hydroxy-2′ 6′ 6′-trimethylcyclohex-2-enyl)-6-methyl- oct-3E 5E 7E-trien-2-one.
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