98748-93-7Relevant academic research and scientific papers
Regiospecific Opening of Oxetanes with Trimethylsilyl Cyanide - Zinc Iodide. A General Approach to γ-Amino Alcohols.
Gassman, Paul G.,Haberman, Leonard M.
, p. 4971 - 4974 (1985)
Trimethylsilyl ethers of γ-hydroxy isonitriles were formed regiospecifically in the opening of oxetanes with trimethylsilyl cyanide - zinc iodide.Deprotection and hydrolysis of the initially formed ring cleavage products gave γ-amino alcohols.
ZINC IODIDE CATALYZED REACTION OF OXETANES WITH TRIMETHYLSILYL CYANIDE
Carr, Steve A.,Weber, William P.
, p. 775 - 782 (2007/10/02)
Oxatanes react regiospecifically with trimethylsilyl cyanide under zinc iodide catalysis to give high yields of 3-trimethylsiloxypropyl isocyanides.
