Synthesis of Highly Functionalized Pyrrolidines via a Mild One-Pot, Three-Component 1,3-Dipolar Cycloaddition Process
Author:
Affiliation:
1. Department of Chemistry, Case Western Reserve University, Cleveland, Ohio 44106-7078 ppg@case.edu
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo051926y
Reference32 articles.
1. 1,3-Dipolar cycloaddition reactions of imines of α-amino-acid esters: X-ray crystal and molecular structure of methyl 4-(2-furyl)-2,7-diphenyl-6,8-dioxo-3,7-diazabicyclo[3.3.0]octane-2-carboxylate
2. Reactivite dipolaire-1,3 d'imines derivees d'α-amino-acides.
3. (a) Grigg, R.; Sridharan, V. InAdvances in Cycloaddition; Curran D. P., Ed.; JAI Press: Greenwich CT, 1993; Vol 3, p 161.
4. (b) Kanemesa, S.; Tsuge, O. InAdvances in Cycloaddition; Curran D. P., Ed.; JAI Press: Greenwich CT, 1993; Vol 3, p 99.
5. Metal-Assisted Stereocontrol of 1,3-Dipolar Cycloaddition Reactions
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