Design principles of the use of alkynes in radical cascades
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Chemical Engineering,General Chemistry
Link
https://www.nature.com/articles/s41570-023-00479-w.pdf
Reference182 articles.
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3. Alabugin, I. V. & Gold, B. “Two functional groups in one package”: using both alkyne π-bonds in cascade transformations. J. Org. Chem. 78, 7777–7784 (2013). Design and control of cascade transformations utilizing both alkyne π-bonds with the formation of up to six new bonds.
4. Gharpure, S. J. & Porwal, S. K. Topologically driven tandem radical cyclization-based strategy for the synthesis of oxa- and aza-cages. Tetrahedron Lett. 50, 7162–7165 (2009).
5. Tsuchii, K., Doi, M., Hirao, T. & Ogawa, A. Highly selective sequential addition and cyclization reactions involving diphenyl diselenide, an alkyne, and alkenes under visible-light irradiation. Angew. Chem. Int. Edn 42, 3490–3493 (2003).
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