A theoretical investigation of the regio- and stereoselectivities of the [3 + 2] cycloaddition reaction between ethyl vinyl ether and substituted α-alkoxynitrones
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry
Link
https://link.springer.com/content/pdf/10.1007/s00214-022-02874-w.pdf
Reference65 articles.
1. Padwa A, Bur S (2016) Recent advances of 1,3-Dipolar cycloaddition chemistry for alkaloid synthesis. Heterocycl Chem. https://doi.org/10.1016/bs.aihch.2016.03.005
2. Ríos-Gutiérrez M, Domingo LR (2019) Unravelling the mysteries of the [3+2] cycloaddition reactions. Eur J Org Chem. https://doi.org/10.1002/ejoc.201800916
3. Nicolaou KC, Snyder SA, Montagnon T, Vassilikogiannakis G (2002) The Diels-Alder reaction in total synthesis. Angew Chem Int Ed 41:1668–1698. https://doi.org/10.1002/1521-3773(20020517)41:10%3c1668::aid-anie1668%3e3.0.co;2-z
4. Padwa A (1984) 1,3-dipolar cycloaddition chemistry. Wiley, New York. https://doi.org/10.1002/jhet.5570230658
5. Rosella CE, Harper JB (2009) The effect of ionic liquids on the outcome of nitrile oxide cycloadditions. Tetrahedron Lett 50(9):992–994. https://doi.org/10.1016/j.tetlet.2008.12.045
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