1,2,3-Triazole: Unique Ligand in Promoting Iron-Catalyzed Propargyl Alcohol Dehydration
Organic Letters2012Vol. 14(9), pp. 2358–2361
Citations Over TimeTop 10% of 2012 papers
Abstract
A 1,2,3-traizole-promoted iron(III)-catalyzed propargyl alcohol dehydration was developed for the synthesis of conjugated enynes. The desired conjugated enynes were prepared in good to excellent yields (up to 95%) with a large substrate scope and excellent stereoselectivity (only Z-isomers).
Related Papers
- → Highly efficient synthesis of propargyl- and allenyltitanium reagents from propargyl halides or propargyl alcohol derivatives. Practical synthesis of allenyl and homopropargyl alcohols(1995)105 cited
- → Reaction of Fe3(CO)12 with but-2-yn-1,4-diol, 1,4-dichloro-but-2-yne, propargyl-alcohol and propargyl-chloride.(2005)17 cited
- → Studies on Derivatives of Propargyl Alcohol. II-III. II. On Propargyl-mercaptan and its Derivatives.(1956)6 cited
- → ChemInform Abstract: Highly Efficient Synthesis of Propargyl‐ and Allenyltitanium Reagents from Propargyl Halides or Propargyl Alcohol Derivatives. Practical Synthesis of Allenyl and Homopropargyl Alcohols.(1995)
- → Studies on Derivatives of Propargyl Alcohol. IV. The Oxidative Coupling and Hydration of Propargyl Amine Derivatives.(1957)