Issue 1, 2021

Synthesis of spirocyclic heterocycles from α,β-unsaturated N-acyliminium ions

Abstract

The reactions of α,β-unsaturated N-acyliminium ions, generated in situ from 4(S)-O-substitutedhydroxy-5-hydroxy-5-vinyl-N-alkylpyrrolidin-2-ones, with allylsilanes and indoles leading to the formation of spirocyclic heterocycles, are reported. Six single crystal X-ray structures and extensive 2D NMR experiments confirmed the structures and stereochemistries of these products. In addition, computational studies provided mechanistic insights and an understanding of the stereochemical outcomes of these reactions.

Graphical abstract: Synthesis of spirocyclic heterocycles from α,β-unsaturated N-acyliminium ions

Supplementary files

Article information

Article type
Paper
Submitted
12 Oct 2020
Accepted
11 Nov 2020
First published
11 Nov 2020

Org. Biomol. Chem., 2021,19, 259-272

Synthesis of spirocyclic heterocycles from α,β-unsaturated N-acyliminium ions

T. Thaima, A. Yazici, C. Auranwiwat, A. C. Willis, U. Wille, T. Limtharakul and Stephen. G. Pyne, Org. Biomol. Chem., 2021, 19, 259 DOI: 10.1039/D0OB02075C

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