Salen–scandium(III) complex-catalyzed asymmetric (3 + 2) annulation of aziridines and aldehydes

Oxazolidine is one of the crucial structural moieties of biologically active compounds. A salen-scandium triflate complex-catalyzed asymmetric (3 + 2) annulation of dialkyl 1-sulfonylaziridine-2,2-dicarboxylates and aldehydes generated optically active functionalized oxazolidine derivatives in moderate to good yields and good to excellent enantioselectivities and high diastereoselectivities. A reasonable reaction mechanism was proposed and rationalized the experimental results.

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Publication Details

Journal
Beilstein Journal of Organic Chemistry
Published
2025-05-28
DOI
https://doi.org/10.3762/bjoc.21.86
Citations
1
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
0.94

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article

Salen–scandium(III) complex-catalyzed asymmetric (3 + 2) annulation of aziridines and aldehydes

Longteng Wang, Jiaxi Xu
1 citations
Beilstein Journal of Organic Chemistry
Synthesis and Catalytic Reactions
0.94
article

Salen–scandium(III) complex-catalyzed asymmetric (3 + 2) annulation of aziridines and aldehydes

Longteng Wang, Jiaxi Xu
article en
1 citations

Abstract

Oxazolidine is one of the crucial structural moieties of biologically active compounds. A salen-scandium triflate complex-catalyzed asymmetric (3 + 2) annulation of dialkyl 1-sulfonylaziridine-2,2-dicarboxylates and aldehydes generated optically active functionalized oxazolidine derivatives in moderate to good yields and good to excellent enantioselectivities and high diastereoselectivities. A reasonable reaction mechanism was proposed and rationalized the experimental results.

Beilstein Journal of Organic ChemistryVol. 21
Beijing University of Chemical Technology (CN)
National Key Research and Development Program of China
Openalex Percentile: Top 26%
Synthesis and Catalytic Reactions
0.94
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