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Nucleoside adducts of vinylporphyrins and vinylchlorins

  • University of California at Davis

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Ethene-linked nucleoside derivatives of porphyrins and chlorins have been synthesized by palladium-catalysed coupling between acetylated 5-chloromercuriuridine and various vinylporphyrins and vinylchlorins. The formation of both the trans- (e.g. 22, 24, 29) and gem- (e.g. 23, 30) isomeric products was usually observed in these coupling reactions, and ratios of these isomers were dependent upon the particular substrate employed.

Original languageEnglish
Pages (from-to)1607-1615
Number of pages9
JournalJournal of the Chemical Society, Perkin Transactions 1
Issue number13
DOIs
StatePublished - Jul 7 1996

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