The synthesis of functionalized pyranophenalenones View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2009-05

AUTHORS

Mohammad B. Teimouri, Reihaneh Bazhrang

ABSTRACT

Protonation of the highly reactive 1:1 intermediate produced in the reaction between alkyl or aryl isocyanides and electron-deficient acetylenic esters with 3-hydroxy-1H-phenalene-1-one leads to a vinylisonitrilium cation, which undergoes an addition reaction with the conjugate base of the 3-hydroxy-1H-phenalene-1-one to produce biologically interesting dialkyl 10-(alkyl or arylamino)-7-oxo-7H,8H-naphtho[1,8-gh]chromene-8,9-dicarboxylates in moderate to fairly good yields at room temperature. More... »

PAGES

513-517

References to SciGraph publications

  • 1996-08. A facile route to highly functionalized ketenimines in MONATSHEFTE FÜR CHEMIE - CHEMICAL MONTHLY
  • 1981. Naturally Occurring Phenalenones and Related Compounds in FORTSCHRITTE DER CHEMIE ORGANISCHER NATURSTOFFE / PROGRESS IN THE CHEMISTRY OF ORGANIC NATURAL PRODUCTS
  • 2008-08. An efficient three-component reaction involving [3 + 1 + 1] furannulation leading to furanonaphthoquinones in water in MONATSHEFTE FÜR CHEMIE - CHEMICAL MONTHLY
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    http://scigraph.springernature.com/pub.10.1007/s00706-008-0082-6

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    http://dx.doi.org/10.1007/s00706-008-0082-6

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