New Oxidative Transformations of Phenolic and Indolic Oxazolines:  An Avenue to Useful Azaspirocyclic Building Blocks

Author:

Braun Norbert A.1,Ousmer Malika1,Bray Jonathan D.1,Bouchu Denis1,Peters Karl1,Peters Eva-Maria1,Ciufolini Marco A.1

Affiliation:

1. Department of Chemistry, MS 60, Rice University, 6100 Main Street, Houston, Texas 77005-1892, Laboratoire de Synthèse et Méthodologie Organiques, Université Claude Bernard Lyon 1 et École Supérieure de Chimie, Physique, Electronique de Lyon, 43, Boulevard du 11 Novembre 1918, 69622 Villeurbanne cedex, France, and Max-Planck-Institut für Festkörperforschung, Heisenbergstrasse 1, 70506 Stuttgart, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Reference41 articles.

1. FR901483, a Novel Immunosuppressant Isolated from Cladobotryum sp. No. 11231. Taxonomy of the Producing Organism, Fermentation, Isolation,Physico-chemical Properties and Biological Activities.

2. Hypervalent iodine oxidation of p-alkoxyphenols and related compounds: a general route to p-benzoquinone monoacetals and spiro lactones

3. (a) Knapp S. InAdvances in Heterocyclic Natural Product Synthesis; Pearson, W. H., Ed.; JAI Press:  Greenwich, CT, 1996; Vol. 3, p 57. It is well recognized that imidates react preferentially at nitrogen with a variety of electrophiles; cf.

4. (b) Tennant, G. InComprehensive Organic Chemistry; Barton, D. H. R., Ollis, W. D., Eds.; Pergamon Press:  Oxford, UK, 1979; Vol. 2, Chapter 8, pp 385−590, see esp. pp 490 ff.

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