massadine

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2003-2017
012320032017

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
The carbocyclic core of massadine has been synthesized relying on a stereoselective formal [3 + 2] cycloaddition of… (More)
  • figure 1
  • table 1
Is this relevant?
2014
2014
Sherman et al. commented on the precedence of enantiodivergence, listing a number of congeneric natural products with opposite… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
2011
2011
A rapid method to access the densely functionalized core structure of massadine (1) has been developed. The use of the Ugi-4… (More)
Is this relevant?
2011
2011
Massadine is a hexacyclic marine natural product, which belongs to the family of pyrrole-imidazole alkaloids. Herein, we describe… (More)
Is this relevant?
Review
2008
Review
2008
The palau’amines, massadines (1-2, Figure 1A), axinellamines (3-4), and the tetrameric stylissadines are pyrrole-imidazole… (More)
  • figure 1
Is this relevant?
2008
2008
functionalized, stereochemically rich alkaloids have made them veritable targets for synthesis studies. Herein we report an… (More)
  • figure 1
  • figure 2
Is this relevant?
2007
2007
Intramolecular Diels-Alder reactions of several N-O linked 4-vinylimidazole dimers provide the expected adduct in moderate to… (More)
Is this relevant?
2007
2007
The distribution of the P2X7 receptor in inflammatory cells suggests that P2X7 antagonists have a significant role to play in the… (More)
Is this relevant?
2003
2003
Massadine, a highly oxygenated alkaloid, was isolated from the marine sponge Stylissa aff. massa as an inhibitor of… (More)
Is this relevant?