Solid phase synthesis of 1,2-disubstituted alkenes: A novel alkynyldihydropyridine to alkenylpyridine isomerization

被引:5
作者
Chen, CX [1 ]
Wang, BW [1 ]
Munoz, B [1 ]
机构
[1] Merck Res Labs, San Diego, CA 92131 USA
关键词
solid-phase synthesis; 1,2-disubstituted alkenes; alkynyldihydropyridine; alkenylpyridine; isomerization;
D O I
10.1055/s-2003-43343
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of 1,2-disubstituted pyridylalkenes have been prepared using a solid-phase resin approach. This approach takes advantage of a novel alkynyldihydropyridine to alkenylpyridine isomerization.
引用
收藏
页码:2404 / 2406
页数:3
相关论文
共 14 条
[1]  
Baldwin JJ, 1998, COMBINATORIAL CHEMISTRY AND MOLECULAR DIVERSITY IN DRUG DISCOVERY, P181
[2]   Combinatorial approaches in anticancer drug discovery: Recent advances in design and synthesis [J].
Bhattacharyya, S .
CURRENT MEDICINAL CHEMISTRY, 2001, 8 (12) :1383-1404
[3]   Solid phase synthesis of 2,4-disubstituted pyridine and tetrahydropyridine derivatives: Resin activation capture approach REACAP technology [J].
Chen, CX ;
Munoz, B .
TETRAHEDRON LETTERS, 1998, 39 (21) :3401-3404
[4]   Solid phase synthesis of N-acyl-2-substituted-dihydro-4-pyridone:: Resin activation capture approach REACAP technology [J].
Chen, CX ;
Munoz, B .
TETRAHEDRON LETTERS, 1998, 39 (38) :6781-6784
[5]   Synthesis of dihydropyridone scaffolds on solid support: Resin activation capture approach REACAP technology [J].
Chen, CX ;
McDonald, IA ;
Munoz, B .
TETRAHEDRON LETTERS, 1998, 39 (3-4) :217-220
[6]   Solid phase synthesis of 2-acyl-3,7,8-substituted-5-oxo-2-azabicyclo[2.2.2]octane and triaza analogs: Resin activation capture approach REACAP technology [J].
Chen, CX ;
Munoz, B .
TETRAHEDRON LETTERS, 1999, 40 (18) :3491-3494
[7]   Solid-phase synthesis of novel isoxazolocyclobutanones and isoxazolinocyclobutenones [J].
Cheng, WC ;
Wong, M ;
Olmstead, MM ;
Kurth, MJ .
ORGANIC LETTERS, 2002, 4 (05) :741-744
[8]   2-methyl-6-(phenylethynyl)-pyridine (MPEP), a potent, selective and systemically active mGlu5 receptor antagonist [J].
Gasparini, F ;
Lingenhöhl, K ;
Stoehr, N ;
Flor, PJ ;
Heinrich, M ;
Vranesic, I ;
Biollaz, M ;
Allgeier, H ;
Heckendorn, R ;
Urwyler, S ;
Varney, MA ;
Johnson, EC ;
Hess, SD ;
Rao, SP ;
Sacaan, AI ;
Santori, EM ;
Veliçelebi, G ;
Kuhn, R .
NEUROPHARMACOLOGY, 1999, 38 (10) :1493-1503
[9]   Novel strategies for solid-phase construction of small-molecule combinatorial libraries [J].
Lou, B .
DRUG DISCOVERY TODAY, 2001, 6 (24) :1288-1294
[10]  
Munoz B, 2000, BIOTECHNOL BIOENG, V71, P78, DOI 10.1002/(SICI)1097-0290(200024)71:1<78::AID-BIT11>3.3.CO