4.8 Article

Catalytic cyclopropanation of alkenes using diazo compounds generated in situ. A novel route to 2-arylcyclopropylamines

Journal

ORGANIC LETTERS
Volume 3, Issue 17, Pages 2785-2788

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol0164177

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[GRAPHICS] A user-friendly, one-pot process for catalytic cyclopropanation of alkenes from tosylhydrazones is described. The cyclopropanation of N-vinylphthalimide provides a new route to 2-arylcyclopropylamines, and this is exemplified in the efficient synthesis of the HIV-1 reverse transcriptase inhibitor 6.

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