Benzyltrimethylammonium hydroxide catalysed nitroaldol condensation

被引:25
作者
Bulbule, VJ [1 ]
Jnaneshwara, GK [1 ]
Deshmukh, RR [1 ]
Borate, HB [1 ]
Deshpande, VH [1 ]
机构
[1] Natl Chem Lab, Div Organ Chem, Pune 411008, Maharashtra, India
关键词
D O I
10.1081/SCC-100107010
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Benzyltrimethylammonium hydroxide is found to be a very efficient catalyst for nitroaldol condensation in a short time with excellent yield.
引用
收藏
页码:3623 / 3626
页数:4
相关论文
共 18 条
[1]  
Adam W, 1998, SYNLETT, P1335
[2]  
Ballini R, 1998, EUR J ORG CHEM, V1998, P355, DOI 10.1002/(SICI)1099-0690(199802)1998:2<355::AID-EJOC355>3.0.CO
[3]  
2-2
[4]  
Ballini R, 1998, SYNLETT, P1049
[5]  
Ballini R, 1999, EUR J ORG CHEM, V1999, P87
[6]   Nitroaldol reaction in aqueous media: An important improvement of the Henry reaction [J].
Ballini, R ;
Bosica, G .
JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (02) :425-427
[7]  
BALLINI R, 1987, SYNTHESIS-STUTTGART, P711
[8]  
BARRETT AGM, 1988, TETRAHEDRON LETT, V29, P5735
[9]   Heterogeneous Henry reaction of aldehydes: Diastereoselective synthesis of nitroalcohol derivatives over Mg-Al hydrotalcites. [J].
Bulbule, VJ ;
Deshpande, VH ;
Velu, S ;
Sudalai, A ;
Sivasankar, S ;
Sathe, VT .
TETRAHEDRON, 1999, 55 (30) :9325-9332
[10]   Oxone® promoted Nef reaction.: Simple conversion of nitro group into carbonyl [J].
Ceccherelli, P ;
Curini, M ;
Marcotullio, MC ;
Epifano, F ;
Rosati, O .
SYNTHETIC COMMUNICATIONS, 1998, 28 (16) :3057-3064