HIGHLY REGIOSELECTIVE INTRAMOLECULAR BIARYL COUPLING REACTION OF A PHENYL BENZOATE DERIVATIVE FOR THE SYNTHESIS OF GRAPHISLACTONE G

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Publication date

January 2012

DOI

10.3987/COM-11-S(P)34

Publisher

Japan Institute of Heterocyclic Chemistry

ISSN

0385-5414

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Abstract

The 6H-dibenzo[b,d]pyran-6-one type natural product graphislactone G was synthesized using a palladium-mediated aryl-aryl coupling reaction of the phenyl benzoate derivative. The regioselectivity in the coupling step was also investigated

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HIGHLY REGIOSELECTIVE INTRAMOLECULAR BIARYL COUPLING REACTION OF A PHENYL BENZOATE DERIVATIVE FOR THE SYNTHESIS OF GRAPHISLACTONE G

Abstract

Extracted data

HIGHLY REGIOSELECTIVE INTRAMOLECULAR BIARYL COUPLING REACTION OF A PHENYL BENZOATE DERIVATIVE FOR THE SYNTHESIS OF GRAPHISLACTONE G

Abstract

Extracted data

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