Abstract
A novel polyheterocyclic chemical space, 6H-furo[3,2-f]pyrrolo[1,2-d][1,4]diazepine, was generated by a one-pot four-component coupling reaction where multiple bonds (three C-C, one C-O, and one C-N) were formed through a domino sequence. Two heterocyclic rings (furan and diazepine) were sequentially constructed from the monocyclic pyrrole derivative under environment-friendly reaction conditions to furnish the tricyclic fused scaffold.
Original language | English |
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Pages (from-to) | 15082-15091 |
Number of pages | 10 |
Journal | Journal of Organic Chemistry |
Volume | 85 |
Issue number | 23 |
DOIs | |
Publication status | Published - 2020 Dec 4 |
Bibliographical note
Funding Information:We thank the National Research Foundation of Korea (NRF-2018R1A6A1A03023718 and NRF-2020R1A2C2005961) for generous financial support.
Publisher Copyright:
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All Science Journal Classification (ASJC) codes
- Organic Chemistry