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Three-Component, Diastereoselective [6 + 3] Annulation of Tropone, Imino Esters, and Arynes.

Authors :
Guin A
Gaykar RN
Deswal S
Biju AT
Source :
Organic letters [Org Lett] 2021 Oct 01; Vol. 23 (19), pp. 7456-7461. Date of Electronic Publication: 2021 Sep 12.
Publication Year :
2021

Abstract

A transition-metal-free, three-component, and diastereoselective [6 + 3] annulation reaction employing tropone, imino esters, and arynes allowing the synthesis of bridged azabicyclo[4.3.1]decadienes is demonstrated. The key nitrogen ylides for the [6 + 3] annulation were generated by the addition of imino esters to the arynes followed by a proton transfer. The nitrogen ylides undergo a regioselective addition to tropone to furnish the desired products in moderate to good yields with good functional group tolerance under mild conditions.

Details

Language :
English
ISSN :
1523-7052
Volume :
23
Issue :
19
Database :
MEDLINE
Journal :
Organic letters
Publication Type :
Academic Journal
Accession number :
34510902
Full Text :
https://doi.org/10.1021/acs.orglett.1c02662