Total Synthesis of (±)-Biphyscion

A regiospecific total synthesis of (±)-biphyscion (1) is described. A novel aspect of the plan was construction of the bianthraquinone ring system from a biphenyl intermediate through the use of a one-pot, double isobenzofuranone condensation.

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Bibliographic Details
Published inOrganic letters Vol. 1; no. 4; pp. 671 - 672
Main Authors Hauser, Frank M, Gauuan, Polivina Jolicia F
Format Journal Article
LanguageEnglish
Published WASHINGTON American Chemical Society 26.08.1999
Amer Chemical Soc
Subjects
Anthraquinones - chemical synthesis
Chemistry
Chemistry, Organic
Magnetic Resonance Spectroscopy
Physical Sciences
Science & Technology
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Summary:A regiospecific total synthesis of (±)-biphyscion (1) is described. A novel aspect of the plan was construction of the bianthraquinone ring system from a biphenyl intermediate through the use of a one-pot, double isobenzofuranone condensation.
Bibliography:Medline
NIH RePORTER
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1523-7060
1523-7052
DOI:10.1021/ol990758r