Alkaloids from the leaves of Daphniphyllum longeracemosum

Journal of Natural Products

Volumn 69, Issue 7, 2006, Pages 1074-1076

  Di, Ying Tong ^a   He, Hong Ping ^a   Lu, Yang ^b   Yi, Ping ^a   Li, Lin ^a   Wu, Li ^b   Hao, Xiao Jiang ^a  

^a KUNMING INSTITUTE OF BOTANY   (China)

^b INSTITUTE OF MATERIA MEDICA   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID DERIVATIVE; DAPHNIPHYLLUM LONGERACEMOSUM EXTRACT; KETONE DERIVATIVE; LONGERACINPHYLLIN A; LONGERACINPHYLLIN B; PLANT EXTRACT; SECO 10,17 DAPHNILONGERANIN B; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; CRYSTAL STRUCTURE; DAPHNIPHYLLUM LONGERACEMOSUM; ISOLATION PROCEDURE; NONHUMAN; PLANT; PLANT LEAF; X RAY DIFFRACTION;

ALKALOIDS; ANGIOSPERMS; CHINA; CRYSTALLOGRAPHY, X-RAY; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; PLANT LEAVES;

DAPHNIPHYLLUM;

EID: 33747436924     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np060088f     Document Type: Article

References (28)

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28. max = 0.157 e/Å. The crystal structure of 1 was solved by direct methods using SHELXS-97 (Sheldrich, G. M. University of Gottingen: Gottingen, Germany, 1997) and expanded using difference Fourier techniques, refined by the program and method SHELXL-97 (Sheldrich, G. M. University of Gottingen: Gottingen, Germany, 1997) and the full-matrix least-squares calculations. All H atoms were placed in geometrically idealized positions and constrained to ride on their parent atoms. The absolute configuration of this compound was not determined. Crystallographic data for the structure 1 reported in this paper have been deposited with the Cambridge Crystallographic Data Centre (deposition number: 293035). Copies of the data can be obtained, free of charge, on application to the Director, CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (fax: +44-(0)1223-336033 or e-mail: deposit@ccdc.cam.ac.uk).