Treat me gently: For a selective synthesis of the unusually sensitive cyclophanic α-pyrone neurymenolide A, the chosen catalysts must be able to distinguish between six different sites of unsaturation, without scrambling any of the skipped π systems. This challenge was met with a new gold-catalyzed pyrone synthesis in combination with a molybdenum-catalyzed ring-closing alkyne metathesis
A sequence comprising a ring-closing alkyne metathesis of a propargyl alcohol derivative, followed b...
General Information: Unless otherwise noted all commercial materials were used without purification....
Disturbing neighbors: Alkenylgold species with a heteroatom substituent are thought to be key interm...
A concise approach to the algal metabolite 1 is described, which also determines the previously unkn...
3-Oxo-5-alkynoic acid esters, on treatment with a carbophilic catalyst, undergo 6-endo-dig cyclizati...
In an attempt to study the ability of the latest generation of alkyne metathesis catalysts to proces...
Exposure of enynes containing a hydroxyl group at one of the propargylic positions to catalytic amou...
A largely catalysis based approach to optically active haouamine A (−)-1 is presented, which provide...
A reaction cascade comprising a rhodium-catalyzed C−H activation, a subsequent hydrometalation of an...
Out of depression: Indeed, no depressing results are obtained from a gold-catalyzed enyne cycloisome...
A concise and largely catalysis-based approach to the potent algal toxin polycavernoside A (1) is de...
Efforts directed toward the synthesis of a basiliolide/transtaganolide model system are disclosed. A...
The tetracyclic core of the integrastatin natural products has been prepared in a convergent and ra...
Disparate sister compounds: Despite their similarity, significantly different strategies were necess...
Very often ligands are anionic or neutral species. Cationic ones are rare, and, when used, the posit...
A sequence comprising a ring-closing alkyne metathesis of a propargyl alcohol derivative, followed b...
General Information: Unless otherwise noted all commercial materials were used without purification....
Disturbing neighbors: Alkenylgold species with a heteroatom substituent are thought to be key interm...
A concise approach to the algal metabolite 1 is described, which also determines the previously unkn...
3-Oxo-5-alkynoic acid esters, on treatment with a carbophilic catalyst, undergo 6-endo-dig cyclizati...
In an attempt to study the ability of the latest generation of alkyne metathesis catalysts to proces...
Exposure of enynes containing a hydroxyl group at one of the propargylic positions to catalytic amou...
A largely catalysis based approach to optically active haouamine A (−)-1 is presented, which provide...
A reaction cascade comprising a rhodium-catalyzed C−H activation, a subsequent hydrometalation of an...
Out of depression: Indeed, no depressing results are obtained from a gold-catalyzed enyne cycloisome...
A concise and largely catalysis-based approach to the potent algal toxin polycavernoside A (1) is de...
Efforts directed toward the synthesis of a basiliolide/transtaganolide model system are disclosed. A...
The tetracyclic core of the integrastatin natural products has been prepared in a convergent and ra...
Disparate sister compounds: Despite their similarity, significantly different strategies were necess...
Very often ligands are anionic or neutral species. Cationic ones are rare, and, when used, the posit...
A sequence comprising a ring-closing alkyne metathesis of a propargyl alcohol derivative, followed b...
General Information: Unless otherwise noted all commercial materials were used without purification....
Disturbing neighbors: Alkenylgold species with a heteroatom substituent are thought to be key interm...