Stereochemical Editing
- PMID: 36576752
- DOI: 10.1002/anie.202217840
Stereochemical Editing
Abstract
Stereochemical editing has recently risen to prominence, allowing the direct editing of organic molecules with stereocenter(s) to adjust their relative stereochemistry at a late-stage. Several seminal light-driven stereochemical editing reactions such as deracemization and epimerization have been successively developed. Recently, Wendlandt and co-workers reported a versatile photochemical epimerization of unactivated tertiary stereogenic centers to rapidly prepare the stereoisomers that were previously challenging to access.
Keywords: Deracemization; Epimerization; Photocatalysis; Stereochemical Editing; Stereoselective Synthesis.
© 2022 Wiley-VCH GmbH.
References
-
- J. Jurczyk, J. Woo, S. F. Kim, B. D. Dherange , R. Sarpong, M. D. Levin, Nat. Synth. 2022, 1, 352-364.
-
- A. Hölzl-Hobmeier, A. Bauer, A. V. Silva, S. M. Huber, C. Bannwarth, T. Bach, Nature 2018, 564, 240-243.
-
- N. Y. Shin, J. M. Ryss, X. Zhang, S. J. Miller, R. R. Knowles, Science 2019, 366, 364-369.
-
- Z. Zhang, X. Hu, Angew. Chem. Int. Ed. 2021, 60, 22833-22838;
-
- Angew. Chem. 2021, 133, 23015-23020.
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