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An Efficient Synthesis of 2-CF3-3-Benzylindoles

An Efficient Synthesis of 2-CF3-3-Benzylindoles

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_0bd7c02548c9445a9eeda508cd9015ca

An Efficient Synthesis of 2-CF3-3-Benzylindoles

About this item

Full title

An Efficient Synthesis of 2-CF3-3-Benzylindoles

Publisher

Basel: MDPI AG

Journal title

Molecules (Basel, Switzerland), 2021-08, Vol.26 (16), p.5084

Language

English

Formats

Publication information

Publisher

Basel: MDPI AG

More information

Scope and Contents

Contents

The reaction of α-CF3-β-(2-nitroaryl) enamines with benzaldehydes afforded effectively α,β-diaryl-CF3-enones having nitro group. Subsequent reduction of nitro group by NH4HCO2-Pd/C system initiated intramolecular cyclization to give 2-CF3-3-benzylindoles. Target products can be prepared in up to quantitative yields. Broad synthetic scope of the rea...

Alternative Titles

Full title

An Efficient Synthesis of 2-CF3-3-Benzylindoles

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_0bd7c02548c9445a9eeda508cd9015ca

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_0bd7c02548c9445a9eeda508cd9015ca

Other Identifiers

ISSN

1420-3049

E-ISSN

1420-3049

DOI

10.3390/molecules26165084

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