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Facile preparation of fluorine-containing 2,3-epoxypropanoates and their epoxy ring-opening reaction...

Facile preparation of fluorine-containing 2,3-epoxypropanoates and their epoxy ring-opening reaction...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_ec2910cac2eb427cb87aa84504b08f69

Facile preparation of fluorine-containing 2,3-epoxypropanoates and their epoxy ring-opening reactions with various nucleophiles

About this item

Full title

Facile preparation of fluorine-containing 2,3-epoxypropanoates and their epoxy ring-opening reactions with various nucleophiles

Publisher

Germany: Beilstein-Institut

Journal title

Beilstein journal of organic chemistry, 2024-09, Vol.20 (1), p.2421-2433

Language

English

Formats

Publication information

Publisher

Germany: Beilstein-Institut

More information

Scope and Contents

Contents

We describe herein a facile method to access 2,3-epoxyesters with fluorine-containing substituents at their 3-position starting from the corresponding enoates by utilization of the low-costed and easy-to-handle reagent, NaOCl·5H
O. Because very little has been disclosed about the reactivity of such 2,3-epoxyesters, their epoxy ring opening by a...

Alternative Titles

Full title

Facile preparation of fluorine-containing 2,3-epoxypropanoates and their epoxy ring-opening reactions with various nucleophiles

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_ec2910cac2eb427cb87aa84504b08f69

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_ec2910cac2eb427cb87aa84504b08f69

Other Identifiers

ISSN

1860-5397

E-ISSN

1860-5397

DOI

10.3762/bjoc.20.206

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