Issue 24, 2018

The synthesis of multi-substituted pyrrolidinones via a direct [3 + 2] cycloaddition of azaoxyallyl cations with aromatic ethylenes

Abstract

A novel [3 + 2] cycloaddition reaction of azaoxyallyl cations and aromatic ethylenes has been developed to afford multi-substituted pyrrolidinones in moderate to good yields. This method not only further expands the synthetic utility of α-halo hydroxamates, but also provides an alternative method for the synthesis of bioactive molecules containing pyrrolidinones.

Graphical abstract: The synthesis of multi-substituted pyrrolidinones via a direct [3 + 2] cycloaddition of azaoxyallyl cations with aromatic ethylenes

Supplementary files

Article information

Article type
Communication
Submitted
17 Apr 2018
Accepted
24 May 2018
First published
25 May 2018

Org. Biomol. Chem., 2018,16, 4439-4442

The synthesis of multi-substituted pyrrolidinones via a direct [3 + 2] cycloaddition of azaoxyallyl cations with aromatic ethylenes

Y. Zhang, H. Ma, X. Liu, X. Cui, S. Wang, Z. Zhan, J. Pu and G. Huang, Org. Biomol. Chem., 2018, 16, 4439 DOI: 10.1039/C8OB00899J

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