pentabromopseudilin and propargylamine

pentabromopseudilin has been researched along with propargylamine* in 2 studies

Other Studies

2 other study(ies) available for pentabromopseudilin and propargylamine

Article	Year
Total synthesis of pentabromo- and pentachloropseudilin, and synthetic analogues--allosteric inhibitors of myosin ATPase. Angewandte Chemie (International ed. in English), 2009, Volume: 48, Issue:43 Topics: Allosteric Regulation; Binding Sites; Catalysis; Computer Simulation; Crystallography, X-Ray; Cyclization; Dictyostelium; Hydrocarbons, Chlorinated; Hydrocarbons, Halogenated; Molecular Conformation; Myosins; Pargyline; Propylamines; Pyrroles; Silver	2009
A Re(V)-catalyzed C-N bond-forming route to human lipoxygenase inhibitors. Organic letters, 2005, Jun-09, Volume: 7, Issue:12 [reaction: see text] A regioselective synthesis of propargylamines by the coupling of propargyl alcohols with tosylamines and carbamates catalyzed by an air- and moisture-tolerant rhenium-oxo complex is described. The ability to couple functionalized components allows for convergent approaches to nitrogen-containing heterocyclic compounds such as the marine antibiotic pentabromopseudilin. These compounds were assayed against human lipoxygenase and found to be both potent and selective. Topics: Catalysis; Combinatorial Chemistry Techniques; Humans; Lipoxygenase Inhibitors; Molecular Structure; Organometallic Compounds; Pargyline; Propylamines; Pyrroles; Rhenium; Stereoisomerism; Structure-Activity Relationship	2005

Article

Year

Total synthesis of pentabromo- and pentachloropseudilin, and synthetic analogues--allosteric inhibitors of myosin ATPase.

Angewandte Chemie (International ed. in English), 2009, Volume: 48, Issue:43

Topics: Allosteric Regulation; Binding Sites; Catalysis; Computer Simulation; Crystallography, X-Ray; Cyclization; Dictyostelium; Hydrocarbons, Chlorinated; Hydrocarbons, Halogenated; Molecular Conformation; Myosins; Pargyline; Propylamines; Pyrroles; Silver

2009

A Re(V)-catalyzed C-N bond-forming route to human lipoxygenase inhibitors.

Organic letters, 2005, Jun-09, Volume: 7, Issue:12

[reaction: see text] A regioselective synthesis of propargylamines by the coupling of propargyl alcohols with tosylamines and carbamates catalyzed by an air- and moisture-tolerant rhenium-oxo complex is described. The ability to couple functionalized components allows for convergent approaches to nitrogen-containing heterocyclic compounds such as the marine antibiotic pentabromopseudilin. These compounds were assayed against human lipoxygenase and found to be both potent and selective.

Topics: Catalysis; Combinatorial Chemistry Techniques; Humans; Lipoxygenase Inhibitors; Molecular Structure; Organometallic Compounds; Pargyline; Propylamines; Pyrroles; Rhenium; Stereoisomerism; Structure-Activity Relationship

2005