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ChemInform Abstract: An Efficient Synthesis of 1,2,3,4-Tetrasubstituted Pyrroles via Intramolecular Azomethine Ylide (3 + 2) Dipolar Cycloaddition.

✍ Scribed by M. TOYOTA; Y. NISHIKAWA; K. FUKUMOTO

Book ID
112022696
Publisher
John Wiley and Sons
Year
2010
Weight
32 KB
Volume
26
Category
Article
ISSN
0931-7597

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A stereoselective synthesis of 3-substit
A stereoselective synthesis of 3-substituted hexahydroindeno[2,1-b]pyrroles via an intramolecular azomethine ylide cycloaddition
✍ John D. Harling; Barry S. Orlek πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 422 KB

3-Substituted hexahydroindeno[2,1-b]pyrroles were prepared in a stereoselective manner in high yield v/a an intramolecular azomethine ylide cycloaddition. Olefin geometry in the ylide precursor controlled the stereochemistry at the 3position.