Xinhua Peng

Find an error

Name: 彭新华
Organization: Nanjing University of Science and Technology , China
Department: School of Chemical Engineering
Title: NULL(PhD)
Co-reporter:Jing Sun, Xinhua Peng, Hao Guo
Tetrahedron Letters 2015 Volume 56(Issue 6) pp:797-800
Publication Date(Web):4 February 2015
DOI:10.1016/j.tetlet.2014.12.086
We report herein a new and effective method for additive-free trifluoromethylation of aromatic aldehydes with TMSCF3. Normal acidic hydrolysis for desilylation in the workup process is not required in this transformation. This reaction presents a new environmentally friendly protocol to access trifluoromethylated benzyl alcohols.
Cyclododecanol, 1-hydroperoxy-
Silane, trimethyl[2,2,2-trifluoro-1-(4-nitrophenyl)ethoxy]-
5-BROMO-2-[(2-METHOXYETHYL)AMINO]NICOTINONITRILE
2-{[2-(2-CYCLOPENTYLETHYL)-4-QUINAZOLINYL]SULFANYL}-N-(5-METHYL-1,2-OXAZOL-3-YL)ACETAMIDE
Benzonitrile, 2,4-dimethyl-5-nitro-
a-(trifluoromethyl)-4-Pyridinemethanol
2,2,2-Trifluoro-1-(4-nitrophenyl)ethanol
Silane, trimethyl[(4-phenoxyphenyl)methyl]-
Cycloheptanol, 1-hydroperoxy-
Silane, (9-anthracenylmethyl)trimethyl-