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New pyrrole alkaloids with bulky N-alkyl side chains containing stereogenic centers from Lycium chinense

Title
New pyrrole alkaloids with bulky N-alkyl side chains containing stereogenic centers from Lycium chinense
Authors
Joung Youn U.Kil Y.-S.Nam J.-W.Jin Lee Y.Kim J.Lee D.Lee J.-H.Seo E.-K.
Ewha Authors
서은경윤의중
SCOPUS Author ID
서은경scopus
Issue Date
2013
Journal Title
Helvetica Chimica Acta
ISSN
0018-019XJCR Link
Citation
vol. 96, no. 8, pp. 1482 - 1487
Indexed
SCI; SCIE; SCOPUS WOS scopus
Abstract
Four new pyrrole alkaloids, methyl 2-[2-formyl-5-(methoxymethyl)-1H-pyrrol- 1-yl]propanoate (1), methyl 2-[2-formyl-5-(methoxymethyl)-1H-pyrrol-1-yl]-3-(4- hydroxyphenyl)propanoate (2), dimethyl 2-[2-formyl-5-(methoxymethyl)-1H-pyrrol- 1-yl]butanedioate (3), and dimethyl 2-[2-formyl-5-(methoxymethyl)-1H-pyrrol-1- yl]pentanedioate (4), were isolated from the AcOEt extract of the fruits of Lycium chinense Miller (Solanaceae). The stereogenic center C(2) in the bulky N-alkyl side chain in each of 1-4 seems to hold the H-atoms of nearby CH 2 groups, CH2(7′) and CH2(3) (if R≠H), leading to two different chemical shifts in the 1H-NMR spectrum due to their diastereotopic characteristics. In the 1H-NMR data of each of 2-4, the enhancement of H-C(2) signal was inhibited by the R group, probably due to steric hindrance, and its chemical shift was influenced by the anisotropy effect. The structures of 1-4 were elucidated by analysis of various spectroscopic data, including 1D- and 2D-NMR. Copyright © 2013 Verlag Helvetica Chimica Acta AG, Zürich.
DOI
10.1002/hlca.201200608
Appears in Collections:
약학대학 > 약학과 > Journal papers
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