z-logo
Premium
Synthesis of Functionalized 2‐Trifluoromethylquinolines and their Heteroaromatic Analogues
Author(s) -
Khutoryanskiy Viktor V.,
Biitseva Angelina V.,
Mykhailiuk Pavel K.
Publication year - 2016
Publication title -
asian journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.846
H-Index - 44
eISSN - 2193-5815
pISSN - 2193-5807
DOI - 10.1002/ajoc.201500519
Subject(s) - chemistry , carbamate , protecting group , combinatorial chemistry , organic chemistry , stereochemistry , alkyl
Electron‐rich anilines and amino heterocycles were converted in one step into N ‐protected functionalized aminoethyl 2‐trifluoromethylquinolines and their heteroaromatic analogues. The N‐carbamate protecting group can be easily cleaved under acidic conditions to give the corresponding amines.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here