Carbolines. Part VII. Anisidines, convenient tools to synthesize hydroxy‐β‐carbolines

dc.contributor.authorRocca, P.
dc.contributor.authorMarsais, F.
dc.contributor.authorGodard, A.
dc.contributor.authorQueguiner, G.
dc.contributor.authorAdams, L.A.
dc.contributor.authorAlo, B.I.
dc.date.accessioned2019-08-31T10:42:27Z
dc.date.available2019-08-31T10:42:27Z
dc.date.issued1995-08
dc.description.abstractThe paper describes a convenient synthesis of hydroxy‐β‐carbolines from commercial anisidines based on key steps such as metalation, cross‐coupling and cyclization. The first total synthesis of a major cyto‐toxic constituent of a marine bryozoan is also reported, the 8‐hydroxy‐1‐vinyl‐β‐carboline.en_US
dc.identifier.citationRocca, P., Marsais, F., Godard, A., Quéguiner, G., Adams, L., & Alo, B. (1995). Carbolines. Part VII. Anisidines, convenient tools to synthesize hydroxy‐β‐carbolines. Journal of heterocyclic chemistry, 32(4), 1171-1175.en_US
dc.identifier.urihttps://ir.unilag.edu.ng/handle/123456789/4931
dc.language.isoenen_US
dc.publisherJournal of Heterocyclic Chemistryen_US
dc.subjectResearch Subject Categories::NATURAL SCIENCES::Chemistry::Organic chemistryen_US
dc.subjectsynthesisen_US
dc.subjectanisidinesen_US
dc.subjectcyclizationen_US
dc.subjectcross‐couplingen_US
dc.titleCarbolines. Part VII. Anisidines, convenient tools to synthesize hydroxy‐β‐carbolinesen_US
dc.typeArticleen_US
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