I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
Mild Lewis acid, often used as its diethyl ether complex; for a brief review of this reagent, see: Synlett, 649 (2002). The complex promotes formation of dithioacetals from aldehydes and dithiols: J. Org. Chem., 59, 4665 (1994), Michael additions of silyl enol ethers: J. Org. Chem., 60, 5024 (1995), and rearrangement of epoxides to carbonyl compounds, giving better selectivity than BF3: J. Org. Chem., 61, 1877 (1996). Efficient catalyst for transesterification of ß-keto esters under near-neutral conditions: Synlett, 1338 (2001)./n
The combination with an acyl anhydride is a powerful acylating agent for aromatic compounds under solvent-free conditions: Tetrahedron Lett., 43, 6331 (2002)./n
See also Lithium trifluoromethanesulfonate, 39322./n
해저드 설명서 (EU): H272-H315-H319-H335
May intensify fire; oxidizer. Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
주의 설명서: P221-P210v-P220-P305+P351+P338-P405-P501a
Take any precaution to avoid mixing with combustibles. Keep away from heat Keep/Store away from clothing/combustible materials. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.