Cycloadditions of 3,4-dihydro-2H-pyrrole 1-oxide to methylene-γ-butyrolactones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference36 articles.
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1. A highly efficient and stereoselective cycloaddition of nitrones to N-arylitaconimides;Tetrahedron Letters;2019-09
2. [3 + 2] Dipolar Cycloadditions of Cyclic Nitrones with Alkenes;Organic Reactions;2017-11-28
3. Acid-mediated coupling of γ-hydroxybutenolides and aldehydes: synthesis of a new class of spirocyclic ketal-lactones;Tetrahedron Letters;2012-12
4. Synthesis and reactivity of furoquinolines bearing an external methylene-bond: access to reduced and spirocyclic structures;Organic & Biomolecular Chemistry;2011
5. ChemInform Abstract: Cycloadditions of 3,4-Dihydro-2H-pyrrole 1-Oxide to Methylene-y-butyrolactones.;ChemInform;2010-06-23
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