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Intramolecular Cycloaddition of Azomethine Ylides in the Preparation of Pyrrolidino[2‘,3‘:3,4]pyrrolidino[1,2- a ]benzimidazoles

✍ Scribed by Meng, Liping; Fettinger, James C.; Kurth, Mark J.

Book ID
120342208
Publisher
American Chemical Society
Year
2007
Tongue
English
Weight
101 KB
Volume
9
Category
Article
ISSN
1523-7060

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ChemInform Abstract: Intramolecular Cycl
ChemInform Abstract: Intramolecular Cycloaddition of Azomethine Ylides in the Preparation of Pyrrolidino[2′,3′:3,4]pyrrolidino[1,2-a]benzimidazoles.
✍ Liping Meng; James C. Fettinger; Mark J. Kurth 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 40 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

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 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 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.