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Diastereoselectivity in the OsO4 Catalyzed Dihydroxylation of Tosylamido-3-hexene-2-ol Derivatives
Uppsala University.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.ORCID iD: 0000-0002-9092-261
Uppsala University.
1995 (English)In: Journal of Organic Chemistry, ISSN 0022-3263, E-ISSN 1520-6904, Vol. 60, no 6, 1848-1851 p.1848-1851 p.Article in journal (Refereed) Published
Abstract [en]

The stereochemistry in dihydroxylation of 5-(p-toluenesulfonamido)-3-hexen-2-ol derivatives was studied. The product configuration was assigned by NMR.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 1995. Vol. 60, no 6, 1848-1851 p.1848-1851 p.
Keyword [en]
STEREOCHEMICAL ASSIGNMENT; NATURAL (-)-CODONOPSININE; ROUTE; (+/-)-ARISTEROMYCIN; (+)-CODONOPSININE; (-)-ANISOMYCIN; CONFIGURATION
National Category
Organic Chemistry
Research subject
Chemistry with specialization in Organic Chemistry
Identifiers
URN: urn:nbn:se:uu:diva-69038DOI: 10.1021/jo00111a050OAI: oai:DiVA.org:uu-69038DiVA: diva2:96949
Note

Addresses: UNIV UPPSALA, DEPT ORGAN CHEM, S-75121 UPPSALA, SWEDEN.

Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2017-06-12

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Gogoll, Adolf

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