ChemInform Abstract: One-Pot Preparation of 2,6-Disubstituted 4-(Trifluoromethyl)pyrimidines via the Tandem Cyclization, Dehydration, and Oxidation Reaction of α,β-Unsaturated Trifluoromethyl Ketones Using POCl3-Pyridine-Silica Gel and MnO2 Systems.

ChemInform ◽  
2010 ◽  
Vol 30 (35) ◽  
pp. no-no
Author(s):  
Kazumasa Funabiki ◽  
Hiroko Nakamura ◽  
Masaki Matsui ◽  
Katsuyoshi Shibata
Synlett ◽  
2019 ◽  
Vol 30 (05) ◽  
pp. 605-609 ◽  
Author(s):  
Fa-Guang Zhang ◽  
Jun-An Ma ◽  
Ning Lv ◽  
Yi-Qiang Tian

A one-pot transformation of α,β-unsaturated trifluoromethyl ketones with 2-(phenylsulfinyl)acetamide to give trifluoromethylated 2-pyridones is realized. The reaction proceeds under mild conditions and involves multiple steps in an expeditious and controlled sequence to provide efficient access to a broad range of trifluoromethylated 2-pyridones in moderate to high yields. Moreover, further synthetic manipulations permit the routine synthesis of a diverse array of trifluoromethylated pyridines with good efficiency.


1999 ◽  
Vol 23 (9) ◽  
pp. 574-575
Author(s):  
Firouz Matloubi Moghaddam ◽  
Mohammad Ghaffarzadeh ◽  
Seyed Hossein Abdi-Oskoui

An AICl3–ZnCl2 mixture supported on silica gel is found to be an efficient medium for the Fries rearrangement of acyloxybenzene or naphthalene derivatives in solvent-free conditions under microwave irradiation.


ChemInform ◽  
2010 ◽  
Vol 41 (44) ◽  
pp. no-no
Author(s):  
Gowravaram Sabitha ◽  
N. Mallikarjuna Reddy ◽  
M. Nagendra Prasad ◽  
G. S. K. Raja ◽  
J. S. Yadav

Sign in / Sign up

Export Citation Format

Share Document