Intramolecular Cycloaddition Azomethine Ylides and α-(Trifluoromethyl)styrenes as Dipolarophiles
Author:
Affiliation:
1. Department of Organic Chemistry; University of Valencia; Avda. Vicente Andrés Estellés, s/n 46100 Burjassot Spain
Funder
Ministerio de Economía y Competitividad
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201901098/fullpdf
Reference27 articles.
1. Application of 1,3-Dipolar Reactions between Azomethine Ylides and Alkenes to the Synthesis of Catalysts and Biologically Active Compounds
2. Switching glycosyltransferase UGTBL1 regioselectivity toward polydatin synthesis using a semi-rational design
3. Synthesis of biologically active natural products by [3 + 2] cycloaddition of non-stabilized azomethine ylides (AMY): Concepts and realizations
4. Recent advances in the enantioselective 1,3-dipolar cycloaddition of azomethine ylides and dipolarophiles
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1. (3 + 2) Cycloaddition Reaction of the Endocyclic N-Silyl Enamine and N,N′-Cyclic Azomethine Imine;Organic Letters;2022-03-07
2. Advances in cycloaddition and hydroaddition reaction of α-(trifluoromethyl)styrenes without defluorination: An alternative approach to CF3-containing compounds;Chinese Chemical Letters;2021-11
3. Fluoroalkyl N-sulfonyl hydrazones: An efficient reagent for the synthesis of fluoroalkylated compounds;Science China Chemistry;2021-08-31
4. Synthesis of CF3–Containing Linear Nitriles from α-(Trifluoromethyl)styrenes;Organic Letters;2021-07-23
5. The Crucial Role of S ‐oxidation State on the Selectivity and Reaction Rate of the 1,3‐Dipolar Cycloaddition of Azomethine Ylides and Homochiral Thiazolines;European Journal of Organic Chemistry;2021-05-26
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