Understanding the regioselectivity and molecular mechanism in the synthesis of isoxazoles containing pentafluorosulfanyl substitution via a [3+2] cycloaddition reaction: A DFT study-Reference-Cited by-同舟云学术

Understanding the regioselectivity and molecular mechanism in the synthesis of isoxazoles containing pentafluorosulfanyl substitution via a [3+2] cycloaddition reaction: A DFT study

Published:2015-10 Issue: Volume:178 Page:165-172
ISSN:0022-1139
Container-title:Journal of Fluorine Chemistry
language:en
Short-container-title:Journal of Fluorine Chemistry

Author:

Emamian Saeedreza

Publisher

Elsevier BV

Subject

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

Reference54 articles.

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2. Synthesis and anticancer activity evaluation of 3,4-mono- and bicyclosubstituted N -(het)aryl trifluoromethyl succinimides

3. Fluorine in medicinal chemistry: Recent therapeutic applications of fluorinated small molecules

4. Fluorine in Medicinal Chemistry

5. Calculation of acidity/basicity values of some fluorinated compounds in gas phase and aqueous solution: A computational approach

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