Formal Cycloaddition Reactions of Vinylogous Amides with α,β-Unsaturated Iminiums. A Strategy for Constructing Piperidinyl Heterocycles
Author:
Affiliation:
1. Department of Chemistry, The University of Minnesota, Minneapolis, Minnesota 55455
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol990107v
Reference13 articles.
1. UMN Undergraduate Research Participant, 1998−1999, and a Recipient of 1998 Pharmacia-Upjohn Summer Research and LANDO-NSF REU Fellowships.
2. Metal-Assisted Cycloaddition Reactions in Organotransition Metal Chemistry
3. Sequential 1,2-Addition−Electrocyclic Ring Closures Involving Acyclic α,β-Unsaturated Iminiums: A Formal [3 + 3] Cycloaddition Strategy to Unique Pyranyl Spirocycles
4. The reactivity of 4-hydroxy-6-methyl-2-pyrone towards different types of ketones
5. A One-Pot Condensation of Pyrones and Enals. Synthesis of 1H,7H-5a,6,8,9-Tetrahydro-1-oxopyrano[4,3-b][1]benzopyrans
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