Regio- and Stereoselectivity of Cycloadditions of Trifluoromethylated Azomethine Ylide
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/67/2/67_2_589/_pdf
Reference7 articles.
1. 1,3-Dipolar cycloadditions. 76. Concerted nature of 1,3-dipolar cycloadditions and the question of diradical intermediates
2. Synthesis of trifluoromethyl azoles using building blocks.
3. 1,3-Dipolar cycloaddition reactions of the geometrical isomers of some methyl 1-alkyl-2-(p-biphenylyl)-3-aziridinecarboxylates
4. Azomethine Ylides from Aziridinedicarboxylic Esters: Kinetics of thecis-trans Isomerization and of the Ring Opening
5. Simple Generation of Ester-Stabilized Azomethine Ylides from 2-Amino Esters and Carbonyl Compounds. Stereochemistry of Their Cycloadditions
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