Aza-Baylis-Hillman reaction of N-tosylated imines with β-substituted α,β-unsaturated esters
被引:39
作者:
Shi, YL
论文数: 0引用数: 0
h-index: 0
机构:
Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organomet Chem, Shanghai 200032, Peoples R ChinaChinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organomet Chem, Shanghai 200032, Peoples R China
Shi, YL
[1
]
Shi, M
论文数: 0引用数: 0
h-index: 0
机构:
Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organomet Chem, Shanghai 200032, Peoples R ChinaChinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organomet Chem, Shanghai 200032, Peoples R China
Shi, M
[1
]
机构:
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organomet Chem, Shanghai 200032, Peoples R China
N-tosylated imine;
Aza-Baylis-Hillman reaction;
beta-substituted activated olefins;
Lewis base;
D O I:
10.1016/j.tet.2005.09.058
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Aza-Baylis-Hillman reaction of N-tosylated imines with beta-substituted alpha,beta-unsaturated esters can take place under mild reaction conditions to give the corresponding Baylis-Hillman adducts in moderate to excellent Yields. (c) 2005 Elsevier Ltd. All rights reserved.