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Ready access to 7,8-dihydroindolo[2,3- d ][1]benzazepine-6(5 H )-one scaffold and analogues via earl...

Ready access to 7,8-dihydroindolo[2,3- d ][1]benzazepine-6(5 H )-one scaffold and analogues via earl...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_c6e0b77b94054f58ad6b18a866173942

Ready access to 7,8-dihydroindolo[2,3- d ][1]benzazepine-6(5 H )-one scaffold and analogues via early-stage Fischer ring-closure reaction

About this item

Full title

Ready access to 7,8-dihydroindolo[2,3- d ][1]benzazepine-6(5 H )-one scaffold and analogues via early-stage Fischer ring-closure reaction

Publisher

Germany: Beilstein-Institut zur Föerderung der Chemischen Wissenschaften

Journal title

Beilstein journal of organic chemistry, 2022, Vol.18 (1), p.143-151

Language

English

Formats

Publication information

Publisher

Germany: Beilstein-Institut zur Föerderung der Chemischen Wissenschaften

More information

Scope and Contents

Contents

Paullone isomers are known as inhibitors of tubulin polymerase and cyclin dependent kinases (Cdks), which are potential targets for cancer chemotherapy. Herein we report an efficient and clean pathway to the fourth isomer, which remained elusive so far, namely 7,8-dihydroindolo[2,3-
][1]benzazepin-6(5
)-one. Moreover, we demonstrate the gener...

Alternative Titles

Full title

Ready access to 7,8-dihydroindolo[2,3- d ][1]benzazepine-6(5 H )-one scaffold and analogues via early-stage Fischer ring-closure reaction

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_c6e0b77b94054f58ad6b18a866173942

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_c6e0b77b94054f58ad6b18a866173942

Other Identifiers

ISSN

1860-5397,2195-951X

E-ISSN

1860-5397

DOI

10.3762/bjoc.18.15

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