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A stereoselective synthesis of 3-substituted hexahydroindeno[2,1-b]pyrroles via an intramolecular azomethine ylide cycloaddition

✍ Scribed by John D. Harling; Barry S. Orlek

Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
422 KB
Volume
54
Category
Article
ISSN
0040-4020

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✦ Synopsis

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.

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