110598-64-6Relevant academic research and scientific papers
HIGH DIASTEREOSELECTIVITY OBSERVED IN THE VINYLATION REACTION OF α,β-EPOXY ALDEHYDES WITH β-SILYLPHOSPHOROUS YLIDE
Iio, Hideo,Mizobuchi, Tsukasa,Tokoroyama, Takashi
, p. 2379 - 2382 (2007/10/02)
The high erythro diastereofacial selectivities were observed in the silyl group migrative vinylation of α,β-epoxy aldehydes substituted by an alkyl or silyl group at the β-position using 2-diphenylmethylsilylethylidene-tris(4-methoxyphenyl)phosphorane.
CARBONYL ADDITION REACTION BY MEANS OF β-SILYLPHOSPHOROUS YLIDE. ANTI-DIASTEREOSELECTIVE VINYLATION OF α-ALKOXY ALDEHYDES.
Iio, Hideo,Mizobuchi, Tsukasa,Tsukamoto, Masamitsu,Tokoroyama, Takashi
, p. 6373 - 6376 (2007/10/02)
β-Silylphosphorous ylide 1c reacts with α-alkoxy aldehydes 2 to give exclusively vinylation product 3, with high anti-diastereoselectivity.
