Nickel-Catalyzed ortho-C‑H Thiolation of N‑Benzoyl α‑Amino Acid Derivatives
We developed the first nickel-catalyzed direct ortho-thiolation of N-benzoyl α-amino acid derivatives. This novel strategy showed wide generality, functional tolerance, and high regioselectivity. In addition, dipeptide derivatives were also compatible with this transformation system, providing a pot...
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Veröffentlicht in: | Journal of organic chemistry 2016-10, Vol.81 (19), p.9122-9130 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | We developed the first nickel-catalyzed direct ortho-thiolation of N-benzoyl α-amino acid derivatives. This novel strategy showed wide generality, functional tolerance, and high regioselectivity. In addition, dipeptide derivatives were also compatible with this transformation system, providing a potential protocol for the direct modification of peptide derivatives. |
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ISSN: | 0022-3263 1520-6904 |
DOI: | 10.1021/acs.joc.6b01702 |