Regiocontrol in the 1,3-dipolar cycloaddition reactions of mesoionic compounds with acetylenic dipolarophiles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. A new observation of limiting-case 1,3-dipolar cycloaddition. Evidence for a highly unsymmetrical transition-state structure with the reactions of mesoionic compounds
2. Intermolecular 1,3-dipolar cycloadditions of müchnones with acetylenic dipolarophiles: Sorting out the regioselectivity
3. Novel synthesis of 5,6,7,8-tetrahydroindolizines
4. 2-Chloroacrylonitrile as a cyclodipolarophile in 1,3-cycloadditions. 3-Cyanopyrroles
5. An Efficient Approach to Pyrroles and N-Bridgehead Pyrroles by Propargylation/Cycloamination of 4-Amino-1-azabutadiene Derivatives
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