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Microwave-assisted sequential three-component synthesis of pyrrolyl-substituted chromeno[2,3-c]isoqu...

Microwave-assisted sequential three-component synthesis of pyrrolyl-substituted chromeno[2,3-c]isoqu...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2403315157

Microwave-assisted sequential three-component synthesis of pyrrolyl-substituted chromeno[2,3-c]isoquinolin-5-amines

About this item

Full title

Microwave-assisted sequential three-component synthesis of pyrrolyl-substituted chromeno[2,3-c]isoquinolin-5-amines

Publisher

New York: Springer US

Journal title

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2020-04, Vol.56 (4), p.495-498

Language

English

Formats

Publication information

Publisher

New York: Springer US

More information

Scope and Contents

Contents

Sequential one-pot domino reaction of homophthalonitrile, salicylaldehydes, and pyrroles in basic media under MW irradiation results in the formation of novel chromeno[2,3-
c
]isoquinolin-5-amines. The transformation represents a domino sequence that starts with Knoevenagel condensation, followed by two nucleophilic cyclizations, consecutivel...

Alternative Titles

Full title

Microwave-assisted sequential three-component synthesis of pyrrolyl-substituted chromeno[2,3-c]isoquinolin-5-amines

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2403315157

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2403315157

Other Identifiers

ISSN

0009-3122

E-ISSN

1573-8353

DOI

10.1007/s10593-020-02686-5

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