Application of a 5-endo-trig cyclisation in the total synthesis of (+)-preussin

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Abstract

The synthesis of 2,5-syn disubstituted pyrrolidines from N-SES protected aziridines is described. The key step in the methodology is a 5-endo-trig cyclisation. Application of this reaction in the synthesis of (+)-preussin is reported. ©ARKAT-USA, Inc.

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Caldwell, J. J., Craig, D., & East, S. P. (2007). Application of a 5-endo-trig cyclisation in the total synthesis of (+)-preussin. Arkivoc, 2007(12), 67–90. https://doi.org/10.3998/ark.5550190.0008.c06

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