The acid free asymmetric intermolecular α-alkylation of aldehydes in fluorinated alcohols

Research output: Contribution to journalArticlepeer-review

78 Scopus citations

Abstract

The acid free asymmetric intermolecular α-alkylation of aldehydes with alcohols has been discovered using trifluoroethanol as solvent. This unprecedented system affords the enantioenriched functionalized primary alcohols (after NaBH4 reduction) in high yields and good to excellent enantioselectivities with wide substrate scope in the absence of any acid additive.

Original languageEnglish
Pages (from-to)3548-3550
Number of pages3
JournalChemical Communications
Volume48
Issue number29
DOIs
StatePublished - 12 Mar 2012
Externally publishedYes

Fingerprint

Dive into the research topics of 'The acid free asymmetric intermolecular α-alkylation of aldehydes in fluorinated alcohols'. Together they form a unique fingerprint.

Cite this