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Protected indanones by a Heck-Aldol annulation reaction
2002 (English)In: Journal of Organic Chemistry, ISSN 0022-3263, E-ISSN 1520-6904, Vol. 67, no 16, 5854-5856 p.Article in journal (Refereed) PublishedText
Abstract [en]

Monoprotected 3-hydroxyindan-1-ones have been prepared in moderate to good yields by a new tandem reaction involving salicylaldehyde triflates and commercially available 2-hydroxyethyl vinyl ether. This one-pot annulation reaction proceeds in the presence of a palladium bidentate catalyst and results in the formation of two new ring systems.

Place, publisher, year, edition, pages
Uppsala Univ, Dept Organ Pharmaceut Chem, SE-75123 Uppsala, Sweden., 2002. Vol. 67, no 16, 5854-5856 p.
National Category
Organic Chemistry
URN: urn:nbn:se:uu:diva-275418DOI: 10.1021/jo025756qISI: 000177318300053PubMedID: 12153293OAI: oai:DiVA.org:uu-275418DiVA: diva2:900275
Available from: 2016-02-03 Created: 2016-02-03 Last updated: 2016-02-03

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