Non-conventional redox chemistry of dihydropyridines and pyridinium salts

被引:13
作者
Lavilla, R
机构
[1] Univ Barcelona, Organ Chem Lab, Fac Pharm, E-08028 Barcelona, Spain
[2] Parc Cient Barcelona, E-08028 Barcelona, Spain
关键词
D O I
10.2174/1385272043370690
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The classical redox chemistry of the NADH-NAD(+) cofactors and their synthetic analogues (dihydropyridines and pyridinium salts) has been extended to non-biomimetic processes. These involve reactions that bypass the electron transfer processes and alloy the functionalization of the heterocyclic parent systems with a broad variety of carbon-and heteroatom-based functional groups. The scope of the methodology, and its applications to organic synthesis are analyzed.
引用
收藏
页码:715 / 737
页数:23
相关论文
共 99 条
[81]  
SAXTON JE, 1994, CHEM HETEROCYCLIC CO, V25, pCH10
[82]  
SAXTON JE, 1983, CHEM HETEROCYCLIC 4, V25, pCH9
[83]   Manganese(III)-based oxidative free-radical cyclizations [J].
Snider, BB .
CHEMICAL REVIEWS, 1996, 96 (01) :339-363
[84]   RECENT ADVANCES IN THE CHEMISTRY OF DIHYDROPYRIDINES [J].
STOUT, DM ;
MEYERS, AI .
CHEMICAL REVIEWS, 1982, 82 (02) :223-243
[85]  
SZANTAY C, 1994, CHEM HETEROCYCLIC CO, V25, pCH9
[86]  
TAYLOR WI, 1973, VINCA ALKALOIDS BOTA
[87]   STEREOSELECTIVE CATALYTIC DOUBLE OSMYLATION OF 1,2-DIHYDROPYRIDINES LEADING TO AMINO-ARABINOSE AND TO AMINO-ALTROSE DERIVATIVES AND TO POTENTIAL GLYCOSIDASE INHIBITORS [J].
TSCHAMBER, T ;
BACKENSTRASS, F ;
NEUBURGER, M ;
ZEHNDER, M ;
STREITH, J .
TETRAHEDRON, 1994, 50 (04) :1135-1152
[88]  
Tschamber T, 1996, HETEROCYCLES, V42, P669
[89]  
URBANSKI J, 1985, POL J CHEM, V59, P1107
[90]  
UTSUNOMIYA I, 1992, HETEROCYCLES, V33, P349