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

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

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_d7b39121290043369134f85879d5a8ab

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

About this item

Full title

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

Author / Creator

Publisher

Trakehner Str. 7-9, 60487 Frankfurt am Main, Germany: Beilstein-Institut

Journal title

Beilstein journal of organic chemistry, 2025-05, Vol.21 (1), p.1087-1094

Language

English

Formats

Publication information

Publisher

Trakehner Str. 7-9, 60487 Frankfurt am Main, Germany: Beilstein-Institut

More information

Scope and Contents

Contents

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 enantiose...

Alternative Titles

Full title

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

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_d7b39121290043369134f85879d5a8ab

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_d7b39121290043369134f85879d5a8ab

Other Identifiers

E-ISSN

1860-5397

DOI

10.3762/bjoc.21.86

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