School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan.
Molecules. 2013 Dec 13;18(12):15531-40. doi: 10.3390/molecules181215531.
The reaction of 1,1-bis(triflyl)ethylene generated in situ with enolizable carbonyls yielded δ-oxo-1,1-bis(triflyl)alkane derivatives. Their acidities in both the gas and solution phases were determined.
1,1-双(三氟甲基)乙烯原位生成的反应与烯醇化羰基化合物生成了δ-氧代-1,1-双(三氟甲基)烷烃衍生物。测定了它们在气相和溶液相中的酸度。