Synthesis of Non‐canonical Tryptophan Variants via Rh‐catalyzed C−H Functionalization of Anilines
Tryptophan and its non-canonical variants play critical roles in pharmaceutical molecules and various enzymes. Facile access to this privileged class of amino acids from readily available building blocks remains a long-standing challenge. Here, we report a regioselective synthesis of non-canonical tryptophans bearing C4-C7 substituents via Rh-catalyzed annulation between structurally diverse tert-butyloxycarbonyl (Boc)-protected anilines and alkynyl chlorides readily prepared from amino acid building blocks. This transformation harnesses Boc-directed C-H metalation and demetalation to afford a wide range of C2-unsubstituted indole products in a redox-neutral fashion. This umpolung approach compared to the classic Larock indole synthesis offers a novel mechanism for heteroarene annulation and will be useful for the synthesis of natural products and drug molecules containing non-canonical tryptophan residues in a highly regioselective manner.
Authors
- Mohammad R. Seyedsayamdost (ORCID: https://orcid.org/0000-0003-2707-4854)
- Vanessa Y. Ying
- Jonathan Z. Huang
Institutions
- Princeton University (US)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2024-09-12
- DOI
- https://doi.org/10.1002/anie.202414998
- Citations
- 8
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 2.00
Funders
- National Science Foundation
- Life Sciences Research Foundation
- Open Philanthropy Project
- National Institutes of Health