TY - JOUR
T1 - The chiral diamine mediated asymmetric Baylis-Hillman reaction
AU - Hayashi, Yujiro
AU - Tamura, Tomohiro
AU - Shoji, Mitsuru
PY - 2004/8
Y1 - 2004/8
N2 - A chiral diamine, easily prepared from proline, is an effective, asymmetric organic catalyst for the Baylis-Hillman reaction of aldehydes and methyl vinyl ketone, affording adducts with enantio-selectivities up to 75%.
AB - A chiral diamine, easily prepared from proline, is an effective, asymmetric organic catalyst for the Baylis-Hillman reaction of aldehydes and methyl vinyl ketone, affording adducts with enantio-selectivities up to 75%.
KW - Asymmetric synthesis
KW - Baylis-Hillman reaction
KW - Diamines
KW - Enones
KW - Lewis base catalysts
KW - Organic catalysis
UR - http://www.scopus.com/inward/record.url?scp=5144225785&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=5144225785&partnerID=8YFLogxK
U2 - 10.1002/adsc.200404069
DO - 10.1002/adsc.200404069
M3 - Article
AN - SCOPUS:5144225785
SN - 1615-4150
VL - 346
SP - 1106
EP - 1110
JO - Advanced Synthesis and Catalysis
JF - Advanced Synthesis and Catalysis
IS - 9-10
ER -