Issue 73, 2021

3-Nitro-coumarin synthesis via nitrative cyclization of aryl alkynoates using tert-butyl nitrite

Abstract

We report a one-pot metal-free synthesis of 3-nitro-coumarins from aryl alkynoates using TBN (tert-butyl nitrite) as the sole reagent. The radical triggered cyclization and nitration of the aryl alkynoates proceeded in a cascaded manner via nitro radical addition to alkynoates, then 5-exo-trig spirocyclization and ester migration.

Graphical abstract: 3-Nitro-coumarin synthesis via nitrative cyclization of aryl alkynoates using tert-butyl nitrite

Supplementary files

Article information

Article type
Communication
Submitted
27 Jun 2021
Accepted
10 Aug 2021
First published
10 Aug 2021

Chem. Commun., 2021,57, 9228-9231

3-Nitro-coumarin synthesis via nitrative cyclization of aryl alkynoates using tert-butyl nitrite

S. Sau and P. Mal, Chem. Commun., 2021, 57, 9228 DOI: 10.1039/D1CC03415D

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