In situ generation and diels-alder reaction of benzynes derivatives with 5-membered ring heterocycles using a microcapillary flow reactor

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Abstract

The formation of benzynes derivatives from ortho-trimethylsilyl triflates using tetra-n-butylammonium fluoride (TBAF) as the benzyne-forming trigger was achieved in a straightforward flow reactor at room temperature. These benzynes were immediately trapped in Diels-Alder reactions to deliver the desired cycloadducts.

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Khadra, A., & Organ, M. G. (2016). In situ generation and diels-alder reaction of benzynes derivatives with 5-membered ring heterocycles using a microcapillary flow reactor. Journal of Flow Chemistry, 6(4), 293–296. https://doi.org/10.1556/1846.2016.00034

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