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A novel approach to oxoisoaporphine alkaloids via regioselective metalation of alkoxy isoquinolines

A novel approach to oxoisoaporphine alkaloids via regioselective metalation of alkoxy isoquinolines

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_84ff6658adc34d119c11aba8f3bf8ca1

A novel approach to oxoisoaporphine alkaloids via regioselective metalation of alkoxy isoquinolines

About this item

Full title

A novel approach to oxoisoaporphine alkaloids via regioselective metalation of alkoxy isoquinolines

Publisher

Germany: Beilstein-Institut zur Föerderung der Chemischen Wissenschaften

Journal title

Beilstein journal of organic chemistry, 2017-08, Vol.13 (1), p.1564-1571

Language

English

Formats

Publication information

Publisher

Germany: Beilstein-Institut zur Föerderung der Chemischen Wissenschaften

More information

Scope and Contents

Contents

Oxoisoaporphine alkaloids are conveniently prepared via direct ring metalation of alkoxy-substituted isoquinolines at C-1, followed by reaction with iodine. Subsequent Suzuki cross-coupling of the resulting 1-iodoisoquinolines to methyl 2-(isoquinolin-1-yl)benzoates and intramolecular acylation of the corresponding carboxylic acids with Eaton’s rea...

Alternative Titles

Full title

A novel approach to oxoisoaporphine alkaloids via regioselective metalation of alkoxy isoquinolines

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_84ff6658adc34d119c11aba8f3bf8ca1

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_84ff6658adc34d119c11aba8f3bf8ca1

Other Identifiers

ISSN

1860-5397,2195-951X

E-ISSN

1860-5397

DOI

10.3762/bjoc.13.156

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