An enantioselective ambimodal cross-Diels–Alder reaction and applications in synthesis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis
Link
https://www.nature.com/articles/s41929-021-00687-x.pdf
Reference49 articles.
1. Diels, O. & Alder, K. Syntheses in the hydroaromatic series [in German]. Justus Liebigs Ann. Chem. 460, 98–122 (1928).
2. Hoffmann, R. & Woodward, R. B. The conservation of orbital symmetry. Acc. Chem. Res. 1, 17–22 (1968).
3. Corey, E. J. Catalytic enantioselective Diels–Alder reactions: methods, mechanistic fundamentals, pathways and applications. Angew. Chem. Int. Ed. 41, 1650–1667 (2002).
4. Nicolaou, K. C., Snyder, S. A., Montagnon, T. M. & Vassilikogiannakis, G. The Diels–Alder reaction in total synthesis. Angew. Chem. Int. Ed. 41, 1668–1698 (2002).
5. Ose, T. et al. Insight into a natural Diels–Alder reaction from the structure of macrophomate synthase. Nature 422, 185–189 (2003).
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