scholarly journals Occurrence, biological activities and 13C NMR data of amides from Piper (Piperaceae)

Química Nova ◽  
2012 ◽  
Vol 35 (11) ◽  
pp. 2288-2311 ◽  
Author(s):  
Jeferson C. do Nascimento ◽  
Vanderlúcia F. de Paula ◽  
Jorge M. David ◽  
Juceni P. David
2006 ◽  
Vol 1 (4) ◽  
pp. 1934578X0600100 ◽  
Author(s):  
Sebastião F. Palmeira Jünior ◽  
Lucia M. Conserva ◽  
José Maria Barbosa Filho

The present work is a review of the literature of clerodane diterpenes from Croton species. It contains a compilation of 13C NMR data of 83 of these diterpenoids and their biological activities. This review covers a period from 1969 to October 2005 and 224 references are cited.


Molecules ◽  
2021 ◽  
Vol 26 (24) ◽  
pp. 7646
Author(s):  
Yhiya Amen ◽  
Marwa Elsbaey ◽  
Ahmed Othman ◽  
Mahmoud Sallam ◽  
Kuniyoshi Shimizu

Chromone glycosides comprise an important group of secondary metabolites. They are widely distributed in plants and, to a lesser extent, in fungi and bacteria. Significant biological activities, including antiviral, anti-inflammatory, antitumor, antimicrobial, etc., have been discovered for chromone glycosides, suggesting their potential as drug leads. This review compiles 192 naturally occurring chromone glycosides along with their sources, classification, biological activities, and spectroscopic features. Detailed biosynthetic pathways and chemotaxonomic studies are also described. Extensive spectroscopic features for this class of compounds have been thoroughly discussed, and detailed 13C-NMR data of compounds 1–192, have been added, except for those that have no reported 13C-NMR data.


1999 ◽  
Vol 23 (3) ◽  
pp. 202-203
Author(s):  
Daniel A. Fletcher ◽  
Brian G. Gowenlock ◽  
Keith G. Orrell ◽  
David C. Apperley ◽  
Michael B. Hursthouse ◽  
...  

Solid-state and solution 13C NMR data for the monomers and dimers of 3- and 4-substituted nitrosobenzenes, and the crystal structure of E-(4-CIC6H4NO)2 are reported.


1995 ◽  
Vol 315 (1-2) ◽  
pp. 1-14 ◽  
Author(s):  
Hans Karlström ◽  
Mats Nilsson ◽  
Bo Nordén

1990 ◽  
Vol 28 (9) ◽  
pp. 817-819 ◽  
Author(s):  
Rainer Haessner ◽  
Lothar Hennig ◽  
Jerzy Gaca
Keyword(s):  
13C Nmr ◽  

2020 ◽  
Vol 15 (10) ◽  
pp. 1934578X2093378
Author(s):  
Josep Coll Toledano

The present review of NMR spectroscopic structural elucidation data of new compounds isolated from Scutellaria species is focused on the title compounds, displaying a peculiar 13-spiro feature. It contains a compilation of 1H and 13C NMR data of these diterpenoids grouped by similar substitution patterns. Comparing shielding effects pointed out not only the identity of some compounds (already reported) but also potential misassignments and convenient revisions to get unambiguous structural proposals.


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