Application of the Intramolecular Vinylogous Morita−Baylis−Hillman Reaction toward the Synthesis of the Spinosyn A Tricyclic Nucleus

Author:

Mergott Dustin J.1,Frank Scott A.1,Roush William R.1

Affiliation:

1. Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109-1055

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference26 articles.

1. A83543A-D, unique fermentation-derived tetracyclic macrolides

2. (b) Kirst, H. A.; Michel, K. H.; Mynderase, J. S.; Chio, E. H.; Yao, R. C.; Nakatsukasa, W. M.; Boeck, L. D.; Occolowitz, J. L.; Paschal, J. W.; Deeter, J. B.; Thompson, G. D. InFermentation-Derived TetracyclicMacrolides; 1992; pp 214−225.

3. Chemistry of A83543A Derivatives. 1. Oxidations and Reductions of A83543A Aglycon

4. Natural products as insecticides: the biology, biochemistry and quantitative structure-activity relationships of spinosyns and spinosoids

5. Recent advances in the chemistry of spinosyns

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