Reductive coupling of allenyl/allyl carbonate with alkyne under dual cobalt-photoredox catalysis
Skipped dienes are among the most prevalent motifs in a vast array of natural products, medicinal compounds, and fatty acids. Herein, we disclose a straightforward one-step reductive protocol under Co/PC for the synthesis of diverse 1,4-dienes with excellent regio- and stereoselectivity. The protocol employs allenyl or allyl carbonate as π-allyl source, allowing for the direct synthesis of skipped diene with a broad range of alkynes including terminal alkynes, propargylic alcohols, and internal alkynes. The method also demonstrated the biomimetic homologation of natural terpenols into synthetic counterparts via iterative allylation of three-carbon allyl units, employing propargylic alcohol as a readily available alkyne source. Experimental studies, control experiments, and DFT calculations suggest the dual catalytic process generates 1,3-diene from allenyl carbonate, followed by proton and electron transfer leading to Co(II)-π-allyl species prior to the alkyne coupling. The catalytic cycle transitions through Co(II), Co(I), and Co(III).
Authors
- Subhankar Pradhan
- Bholanath Maity (ORCID: https://orcid.org/0000-0001-5969-0112)
- Luigi Cavallo (ORCID: https://orcid.org/0000-0002-1398-338X)
- Basker Sundararaju (ORCID: https://orcid.org/0000-0003-1112-137X)
- Sayan Dutta (ORCID: https://orcid.org/0000-0002-8232-5989)
- Dhananjay Satav
Institutions
- King Abdullah University of Science and Technology (SA)
- Indian Institute of Technology Kanpur (IN)
Publication Details
- Journal
- Nature Communications
- Published
- 2024-11-29
- DOI
- https://doi.org/10.1038/s41467-024-54718-9
- Citations
- 6
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 1.50
Funders
- Indian Institute of Technology Kanpur
- King Abdullah University of Science and Technology
- Science and Engineering Research Board