TUMOUR INHIBITORY PLANTS . AMIDES OF PIPER NOVAE-HOLLANDIAE (PIPERACEAE)

被引:70
作者
LODER, JW
MOORHOUS.A
RUSSELL, GB
机构
[1] Division of Applied Chemistry, CSIRO Chemical Research Laboratories, Melbourne, VIC, 3001
基金
美国国家卫生研究院;
关键词
D O I
10.1071/CH9691531
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new amide, खαβ-dihydropiperine (I), has been isolated from the wood of Piper novae-hollandiae and synthesized. Two amides, N-isobutyl-trans- 2, trans-4-octadienamide and 3,4-methylenedioxycinnamoylpiperidide, previously unreported from natural sources but known from synthesis, were present as were five amides already established as plant constituents, namely, N-isobutyl-trans-2, trans-4-decadienamide, fagaramide, piperlonguminine, piperine, and an isomer of piperine, probably chavicine, as well as the essential oil, dillapiole. खαβ-and खβγ-Dihydro-piperlonguminine, (VIII) and (IX), and खβγ-dihydropiperine (III) were also synthesized. © 1969, CSIRO. All rights reserved.
引用
收藏
页码:1531 / &
相关论文
共 20 条
[1]   368 Derivatives of 1 2 3 4-tetrahydroxybenzene - Part III The synthesis of dill apiole, and the extension of the dakin reaction [J].
Baker, W ;
Jukes, EHT ;
Subrahmanyam, CA .
JOURNAL OF THE CHEMICAL SOCIETY, 1934, :1681-1684
[2]   LOCAL ANOESTHETIC IN FAGARA XANTHOXYLOIDES [J].
BOWDEN, K ;
ROSS, WJ .
JOURNAL OF THE CHEMICAL SOCIETY, 1963, (JUL) :3503-&
[3]  
BUDZIKIEWICZ H, 1967, MASS SPECTROMETRY OR, P336
[4]   ALKALOIDS OF PIPER LONGUM LINN .I. STRUCTURE AND SYNTHESIS OF PIPERLONGUMINE AND PIPERLONGUMININE [J].
CHATTERJEE, A ;
DUTTA, CP .
TETRAHEDRON, 1967, 23 (04) :1769-+
[5]  
CHATTERJEE A, 1966, TETRAHEDRON LETT, P1797
[6]  
Ciamician G, 1896, BER DTSCH CHEM GES, V29, P1799
[7]   AMIDES OF VEGETABLE ORIGIN .4. THE NATURE OF PELLITORINE AND ANACYCLIN [J].
CROMBIE, L .
JOURNAL OF THE CHEMICAL SOCIETY, 1955, :999-1006
[8]   AMIDES OF VEGETABLE ORIGIN .5. STEREOCHEMISTRY OF CONJUGATED DIENES [J].
CROMBIE, L .
JOURNAL OF THE CHEMICAL SOCIETY, 1955, :1007-1025
[9]  
FITTIG R, 1883, LIEBIGS ANN, V216, P171
[10]  
FITTIG R, 1985, LIEBIGS ANN, V227, P31