TY - JOUR
T1 - Simple oxazolidine chiral diene ligands for enantioselective rh-catalyzed conjugate additions
AU - Fairhurst, N.W.G.
AU - Munday, R.H.
AU - Carbery, D.R.
PY - 2013
Y1 - 2013
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84872688131&partnerID=8YFLogxK
UR - http://dx.doi.org/10.1055/s-0032-1318135
U2 - 10.1055/s-0032-1318135
DO - 10.1055/s-0032-1318135
M3 - Article
AN - SCOPUS:84872688131
SN - 0936-5214
VL - 24
SP - 496
EP - 498
JO - Synlett
JF - Synlett
IS - 4
ER -