## Abstract Three new arylnaphthalene lignans, named neojusticin C (1), procumbenoside C (2) and procumbenoside D (3), have been isolated from the whole plant of __Justicia procumbens__, together with three known ones, justicidinoside B (4), justicidinoside C (5), and diphyllin‐1‐__O__‐β‐D‐apiofura
Complete assignments of 1H and 13C NMR data for new dibenzocyclooctadiene lignans from Kadsura oblongifolia
✍ Scribed by Hai-Tao Liu; Li-Jia Xu; Yong Peng; Jun-Shan Yang; Xiu-Wei Yang; Pei-Gen Xiao
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 105 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2430
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Two new dibenzocyclooctadiene lignans, named kadoblongifolins A (1) and B (2), and one new natural product dibenzocyclooctadiene lignan, named kadoblongifolin C (3), were isolated from the stems of Kadsura oblongifolia (K. oblongifolia), together with five known ones, schizanrin F (4), propinquanin C (5), schisantherin G (6), heteroclitin Q (7), kadsurarin (8). The structures of these new lignans were elucidated by a combination of high‐resolution electron ionization mass spectrometry (HR‐EI‐MS), ^1^H NMR, ^13^C NMR, HMQC, HMBC, and NOESY spectra. Copyright © 2009 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
## Abstract The structures of three benzylidenebenzyl butyrolactone lignans (gossypifan, carthamogenin, and savinin) have been established on basis of ^1^H NMR and ^13^C NMR spectroscopic data. The ^1^H NMR and ^13^C NMR spectra of these lignans have been fully assigned by the use of techniques suc
## Abstract Three new arylnaphthalide lignans named 6′‐hydroxy justicidin A (1), 6′‐hydroxy justicidin B (2) and 6′‐hydroxy justicidin C (3) have been isolated from the whole plant of __Justicia procumbens__, together with four known ones, neojusticin A (4), chinensinaphthol methyl ester (5), isodi
## Abstract In this work we describe the complete ^1^H and ^13^C NMR analyses of three arylnaphtalene lignan lactones (taiwanin C, 4‐methyl dehydroretrodendrin and justicidin B) using modern NMR techniques such as gCOSY, nonedited gHSQC, gHMBC and NOE experiments. Complete assignment and homonuclea
## Abstract We describe the complete ^1^H and ^13^C NMR analysis of three aryltetralin lignan lactones (polygamain, morelensin and 4,5‐dimethoxymorelensin) using modern NMR techniques such as COSY, HMQC, HMBC, 2D‐__J__‐resolved and NOE experiments. The relative stereochemistry of these compounds, w
## Abstract In this article we present a complete ^1^H and ^13^C NMR spectral analysis of three 7,7′‐dihydroarylnaphthalene lignan lactones using modern NMR techniques such as COSY, HSQC, HMBC and NOE experiments. Complete assignment and homonuclear hydrogen coupling constant measurements were perf