Site Navigation
Categories:
Carbon-carbon bond forming reactions

Summary Of: Alkyne metathesis

Alkyne metathesis was first observed in 1974... Alkyne metathesis mechanism through a metallacyclobutadiene intermediate... Alkyne metathesis mechanism through a metallacyclobutadiene intermediate... Alkyne metathesis is extensively used in... Alkyne Metathesis in Organic Synthesis...

Encyclodia Page On: Alkyne metathesis

These Are Links To Other Documents
The Mortreux system consists of molybdenum hexacarbonyl resorcinol catalyst system. The phenyl and p-methylphenyl substituents on the alkyne group are scrambled | organic reaction | alkyne | chemical bonds | olefin metathesis | molybdenum | molybdenum hexacarbonyl | resorcinol | R.R. Schrock | timeAlkyne metathesis mechanism through a metallacyclobutadiene intermediate | tungsten | Fischer carbenes | Alkyne metathesis of 2-hexyne with Schrock catalyst, equilibrium after 5 minutes reaction | amidation | tert-butanol | Synthesis of Schrock catalyst starting from tetrachloro tungsten | organometallic | alkoxide | aniline | ligands | A. Fürstner developed a new molybdenum catalyst replacing alkoxy with aryl ligands | ring-closing | olfactory | civetone | stereoselectively | hydrogen | lindlar catalyst | Z-alkene | E-alkenes | Birch reduction | acetylene | 2-butyne | Synthesis of civetone. Step 1 alkyne metathesis, step 2 lindlar reduction | cyclophane | Turriane synthesis. Step 1 alkyne metathesis, step 2 Lindlar reduction, PMB = para-methoxybenzyl protecting group. Microwave assisted reaction takes reaction time down from 6 hours to 5 minutes | tungsten nitride | nitrile | Nitrile-Alkyne Cross-Metathesis | Chemical Communications | doi | J. Am. Chem. Soc. | doi | Organometallics | doi | Chemical Communications | doi | J. Am. Chem. Soc. | doi | Chemical & Engineering News | Category | Carbon-carbon bond forming reactions |
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Alkyne metathesis".