Simple oxazolidine chiral diene ligands for enantioselective rh-catalyzed conjugate additions

N.W.G. Fairhurst, R.H. Munday, D.R. Carbery

Research output: Contribution to journalArticle

6 Citations (Scopus)
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Abstract

Simple oxazolidine-based chiral diene ligands, ultimately derived from serine, have been synthesized using the Seebach self-regeneration of stereocenters strategy. The ligands have been used in the enantioselective Rh-catalyzed conjugate addition of aryl boronic acids to cyclohexenone. An efficient 'in vacuo' reaction protocol has been developed as part of this study.
Original languageEnglish
Pages (from-to)496-498
Number of pages3
JournalSynlett
Volume24
Issue number4
Early online date23 Jan 2013
DOIs
Publication statusPublished - 2013

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Boronic Acids
Ligands
Serine
oxazolidine

Cite this

Simple oxazolidine chiral diene ligands for enantioselective rh-catalyzed conjugate additions. / Fairhurst, N.W.G.; Munday, R.H.; Carbery, D.R.

In: Synlett, Vol. 24, No. 4, 2013, p. 496-498.

Research output: Contribution to journalArticle

Fairhurst, N.W.G. ; Munday, R.H. ; Carbery, D.R. / Simple oxazolidine chiral diene ligands for enantioselective rh-catalyzed conjugate additions. In: Synlett. 2013 ; Vol. 24, No. 4. pp. 496-498.
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