Tetrahedron p. 14905 - 14912 (1998)
Update date:2022-08-04
Topics:
Harling, John D.
Orlek, Barry S.
3-Substituted hexahydroindeno[2,1-b]pyrroles were prepared in a stereoselective manner in high yield via an intramolecular azomethine ylide cycloaddition. Olefin geometry in the ylide precursor controlled the stereochemistry at the 3-position.
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