Regio- and Stereoselective Ring Openings of 3-Aza-2-oxabicyclo[2.2.1]hept-5-ene Systems with Copper Catalyst-Modified Grignard Reagents: Application to the Synthesis of an Inhibitor of 5-Lipoxygenase-Reference-Cited by-同舟云学术

Regio- and Stereoselective Ring Openings of 3-Aza-2-oxabicyclo[2.2.1]hept-5-ene Systems with Copper Catalyst-Modified Grignard Reagents: Application to the Synthesis of an Inhibitor of 5-Lipoxygenase

Published:2002-05-14 Issue:12 Volume:67 Page:4115-4121
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Surman Matthew D.¹,Mulvihill Mark J.¹,Miller Marvin J.¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo016275u

Reference40 articles.

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4. Stereoselective Cycloadditions of Chiral Acyl-Nitroso Compounds

5. On the origin of the diastereoselectivity observed in cycloadditions of chiral acyl-nitroso compounds

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