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).

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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

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article

Reductive coupling of allenyl/allyl carbonate with alkyne under dual cobalt-photoredox catalysis

Subhankar Pradhan, Bholanath Maity, Luigi Cavallo, Basker Sundararaju et al.
6 citations
Nature Communications
Catalytic C–H Functionalization Methods
1.50
article

Reductive coupling of allenyl/allyl carbonate with alkyne under dual cobalt-photoredox catalysis

Subhankar Pradhan, Bholanath Maity, Luigi Cavallo, Basker Sundararaju, Sayan Dutta, Dhananjay Satav
article en
6 citations

Abstract

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).

Nature CommunicationsVol. 15(1)
King Abdullah University of Science and Technology (SA), Indian Institute of Technology Kanpur (IN)
Indian Institute of Technology Kanpur, King Abdullah University of Science and Technology, Science and Engineering Research Board
Clean water and sanitation
Openalex Percentile: Top 18%
Catalytic C–H Functionalization Methods
1.50
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Reductive coupling of allenyl/allyl carbonate with alkyne under dual cobalt-photoredox catalysis — Subhankar Pradhan, Bholanath Maity, et al. · Nature Communications (2024) | TGRS Research Map | TGRS