Sustainable Solvent-Free Diels–Alder Approaches in the Development of Constructive Heterocycles and Functionalized Materials: A Review
Author:
Funder
Council on grants of the President of the Russian Federation
Российский Фонд Фундаментальных Исследований
Publisher
Springer Science and Business Media LLC
Subject
General Chemistry
Link
https://link.springer.com/content/pdf/10.1007/s41061-022-00398-2.pdf
Reference66 articles.
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2. Houk KN, Liu F, Yang Z, Seeman JI (2021) Evolution of the Diels–Alder reaction mechanism since the 1930s: Woodward, Houk with Woodward, and the influence of computational chemistry on understanding cycloadditions. Angew Chem Int Ed 60(23):12660–12681. https://doi.org/10.1002/anie.202001654
3. Huang G, Kouklovsky C, de la Torre A (2020) Inverse-electron-demand Diels–Alder reactions of 2-pyrones: bridged lactones and beyond. Chem Eur J 27:4760–4788. https://doi.org/10.1002/chem.202003980
4. Pałasz A (2016) Recent advances in inverse-electron-demand hetero-Diels–Alder reactions of 1-oxa-1, 3-butadienes. Top Curr Chem 374(3):1–37. https://doi.org/10.1007/s41061-016-0026-2
5. Carey FA, Sundberg RJ (2007) Advanced organic chemistry: part B: reaction and synthesis, 5th edn. Springer, New York. https://doi.org/10.1007/978-0-387-44899-2
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