N–O Tethered Carbenoid Cyclopropanation Facilitates the Synthesis of a Functionalized Cyclopropyl-Fused Pyrrolidine
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, United States
2. Chemical Engineering Department, Hitit University, Corum, Turkey
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo400788a
Reference68 articles.
1. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents
2. Recent Advances in the Total Synthesis of Piperidine and Pyrrolidine Natural Alkaloids with Ring‐Closing Metathesis as a Key Step
3. Highlights of natural product synthesis
4. Recent Advances in the Development of MMPIs and APNIs Based on the Pyrrolidine Platforms
5. Robl, J. A.; Sulsky, R. B.; Augeri, D. J.; Magnin, D. R.; Hamann, L. G.; Betebenner, D. A.Cyclopropyl-fused pyrrolidine-based inhibitors of dipeptidyl peptidase IV. U.S. Patent 6,395,767, May 28, 2002.
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