Asymmetric construction of enantioenriched spiro <i>gem</i>-diamines <i>via</i> [3 + 3] annulation of α,β-unsaturated <i>N</i>-sulfonyl ketimines and 3-aminobenzofurans

A general and facile enantioselective cyclization protocol for α,β-unsaturated N -sulfonyl ketimines and 3-aminobenzofurans has been developed for the construction of enantioenriched spiro gem -diamines.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00145e
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.94
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article

Asymmetric construction of enantioenriched spiro gem-diamines via [3 + 3] annulation of α,β-unsaturated N-sulfonyl ketimines and 3-aminobenzofurans

Tingting Zhang, Shumin Wang, Yongxing Zhang, Yang Wang et al.
1 citations
Organic Chemistry Frontiers
Sulfur-Based Synthesis Techniques
0.94
article

Asymmetric construction of enantioenriched spiro gem-diamines via [3 + 3] annulation of α,β-unsaturated N-sulfonyl ketimines and 3-aminobenzofurans

Tingting Zhang, Shumin Wang, Yongxing Zhang, Yang Wang, Ki Tong, Xin Shu
article en
1 citations

Abstract

A general and facile enantioselective cyclization protocol for α,β-unsaturated N -sulfonyl ketimines and 3-aminobenzofurans has been developed for the construction of enantioenriched spiro gem -diamines.

Organic Chemistry FrontiersVol. 12(12)
Qingdao National Laboratory for Marine Science and Technology (CN), Ocean University of China (CN)
Openalex Percentile: Top 28%
Sulfur-Based Synthesis Techniques
0.94
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