Issue 3, 2021

Asymmetric sequential annulation/aldol process of 4-isothiocyanato pyrazolones and allenones: access to novel spiro[pyrrole–pyrazolones] and spiro[thiopyranopyrrole–pyrazolones]

Abstract

A catalytic asymmetric sequential annulation/aldol reaction of 4-isothiocyanato pyrazolones and allenyl ketones has been developed, which furnished a series of spiro[pyrrole–pyrazolone] heterocycles and structurally novel spiro[thiopyranopyrrole–pyrazolone] derivatives in good yields with high to excellent enantioselectivities. Notably, parallel resolution of racemic spiro[pyrrole–pyrazolones] was achieved by a catalyst-controlled asymmetric intramolecular vinylogous aldol process. Structure diversity of the product was further enhanced by ready transformations.

Graphical abstract: Asymmetric sequential annulation/aldol process of 4-isothiocyanato pyrazolones and allenones: access to novel spiro[pyrrole–pyrazolones] and spiro[thiopyranopyrrole–pyrazolones]

Supplementary files

Article information

Article type
Communication
Submitted
27 Oct 2020
Accepted
02 Dec 2020
First published
08 Dec 2020

Chem. Commun., 2021,57, 363-366

Asymmetric sequential annulation/aldol process of 4-isothiocyanato pyrazolones and allenones: access to novel spiro[pyrrole–pyrazolones] and spiro[thiopyranopyrrole–pyrazolones]

W. Wang, X. Bao, S. Wei, S. Nawaz, J. Qu and B. Wang, Chem. Commun., 2021, 57, 363 DOI: 10.1039/D0CC07113G

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