88511-88-0

Upstream product

• 62889-07-0 trimethyl((1-(thiophen-2-yl)vinyl)oxy)silane 

Downstream Products

• 871024-67-8 2-hydroxy-3-(N-diphenylphosphinoylamino)-3-phenyl-1-(2-thienyl)propan-1-one 
• 1352786-47-0 4-phenyl-1-(thiophen-2-yl)but-3-yne-1,2-dione 
• 40353-41-1 2-(thiophen-2-yl)quinoxaline 

Relevant academic research and scientific papers

Hypervalent Iodine Oxidation of Silyl Enol Ethers. A Direct Route to α-Hydroxy Ketones

Hypervalent iodine oxidation of various silyl enol ethers (aromatic, heteroaromatic, and aliphatic) using iodosobenzene-boron trifluoride diethyl ether-water provides a general and direct route for the α-hydroxylation of ketones.The structures of 2-hydroxy- (8) and 3-hydroxy-acetylpyridine (9) are discussed as well as the scope and mechanism of the reaction.