The experiment is a simple and practical organocatalytic procedure for the enantiose- lective alkylation of aldehydes using a commercially available and stable carbenium ion. The alkylated adduct 4, obtained in high enantiomeric excess, is then transformed into the corresponding enantioen- riched alcohol 5 by reduction of the benzodithiole group with Raney®-nickel.

Pier Giorgio, C., Marco, B., Andrea, G., Luca, M. (2016). A Practical Organocatalytic Alkylation Reaction with Benzodithiolylium Tetrafluoroborate. Cambridge : The Royal Society of Chemistry.

A Practical Organocatalytic Alkylation Reaction with Benzodithiolylium Tetrafluoroborate

COZZI, PIER GIORGIO;BANDINI, MARCO;GUALANDI, ANDREA;MENGOZZI, LUCA
2016

Abstract

The experiment is a simple and practical organocatalytic procedure for the enantiose- lective alkylation of aldehydes using a commercially available and stable carbenium ion. The alkylated adduct 4, obtained in high enantiomeric excess, is then transformed into the corresponding enantioen- riched alcohol 5 by reduction of the benzodithiole group with Raney®-nickel.
2016
Comprehensive Organic Chemistry Experiments for the Laboratory Classroom
120
124
Pier Giorgio, C., Marco, B., Andrea, G., Luca, M. (2016). A Practical Organocatalytic Alkylation Reaction with Benzodithiolylium Tetrafluoroborate. Cambridge : The Royal Society of Chemistry.
Pier Giorgio, Cozzi; Marco, Bandini; Andrea, Gualandi; Luca, Mengozzi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/587250
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