New strategies in the synthesis of regioselectively trifluoromethyl- and trifluoromethoxy-substituted arenes as building blocks for biologically active molecules-Reference-Cited by-同舟云学术

New strategies in the synthesis of regioselectively trifluoromethyl- and trifluoromethoxy-substituted arenes as building blocks for biologically active molecules

Published:2002-10 Issue:2 Volume:117 Page:167-172
ISSN:0022-1139
Container-title:Journal of Fluorine Chemistry
language:en
Short-container-title:Journal of Fluorine Chemistry

Author:

Leconte Stephane,Ruzziconi Renzo

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Environmental Chemistry,Biochemistry

Reference27 articles.

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2. Parametrisierung von Substituenten – der Einfluß von Fluor und anderen Heteroatomen auf OH-, NH- und CH-Aciditäten

3. Parametrization of Substituents: Effects of Fluorine and Other Heteroatoms on OH, NH, and CH Acidities

4. About the “physiological size” of fluorine substituents: Comparison of sensorially active compounds with fluorine and methyl substituted analogues

5. Introduction of fluorine into organic molecules: why and how

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