pyrroles has been researched along with agelastatin a in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (80.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chapuis, JC; Doubek, DL; Ducki, S; Herald, DL; Pettit, GR; Schmidt, JM | 1 |
| Dong, G; Trost, BM | 2 |
| Du Bois, J; Wehn, PM | 1 |
| Batey, RA; Duspara, PA | 1 |
5 other study(ies) available for pyrroles and agelastatin a
| Article | Year |
|---|---|
Antineoplastic agents 470. Absolute configuration of the marine sponge bromopyrrole agelastatin A.
Topics: Alkaloids; Animals; Antineoplastic Agents; Molecular Conformation; Oxazolidinones; Porifera; Pyrroles; X-Ray Diffraction | 2005 |
New class of nucleophiles for palladium-catalyzed asymmetric allylic alkylation. Total synthesis of agelastatin A.
Topics: Alkaloids; Alkylation; Allyl Compounds; Amides; Catalysis; Cyclopentanes; Oxazolidinones; Palladium; Pyrroles; Stereoisomerism | 2006 |
A stereoselective synthesis of the bromopyrrole natural product (-)-agelastatin A.
Topics: Alkaloids; Biological Products; Bromine Compounds; Catalysis; Heterocyclic Compounds, 1-Ring; Molecular Structure; Oxazolidinones; Pyrroles; Rhodamines; Stereoisomerism; Sulfonic Acids; Thiazepines | 2009 |
A stereodivergent strategy to both product enantiomers from the same enantiomer of a stereoinducing catalyst: agelastatin A.
Topics: Alkaloids; Catalysis; Copper; Magnetic Resonance Spectroscopy; Molecular Structure; Organometallic Compounds; Oxazolidinones; Palladium; Pyrroles; Stereoisomerism | 2009 |
A short total synthesis of the marine sponge pyrrole-2-aminoimidazole alkaloid (±)-agelastatin A.
Topics: Alkaloids; Animals; Cyclization; Imidazoles; Oxazolidinones; Porifera; Pyrroles; Stereoisomerism | 2013 |