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Issue 38, 2019
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Photooxygenation of 2-propargylfurans: a path to structurally diverse nitrogen-containing 5-membered rings

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Abstract

The photooxygenation of 2-propargylfurans enabled access to original nitrogen-containing cyclopentenones and related compounds in a one-pot fashion. By employing readily-available substrates such as furans and amines, we succeeded in achieving a high degree of molecular complexity. Relying on the introduction of an alkyne moiety and tailored substrates, this transformation reveals a new facet for reaction sequences featuring the photooxygenation of furans.

Graphical abstract: Photooxygenation of 2-propargylfurans: a path to structurally diverse nitrogen-containing 5-membered rings

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Article information


Submitted
11 Feb 2019
Accepted
04 Apr 2019
First published
04 Apr 2019

Chem. Commun., 2019,55, 5443-5446
Article type
Communication

Photooxygenation of 2-propargylfurans: a path to structurally diverse nitrogen-containing 5-membered rings

L. Marin, G. Force, R. Guillot, V. Gandon, E. Schulz and D. Lebœuf, Chem. Commun., 2019, 55, 5443
DOI: 10.1039/C9CC01197H

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