Comprehensive survey of combinatorial library synthesis: 2001

被引：139
作者：
Dolle, RE [1 ]
机构：
[1] Adolor Corp, Dept Chem, Malvern, PA 19355 USA
来源：
JOURNAL OF COMBINATORIAL CHEMISTRY | 2002年 / 4卷 / 05期
关键词：
D O I：
10.1021/cc020039v
中图分类号：
O69 [应用化学];
学科分类号：
081704 ;
摘要：
引用
收藏
页码：369 / 418
页数：50
相关论文
共 353 条
[1]   Parallel modification of tropane alkaloids [J].
Aberle, NS ;
Ganesan, A ;
Lambert, JN ;
Saubern, S ;
Smith, R .
TETRAHEDRON LETTERS, 2001, 42 (10) :1975-1977
[2]   A novel approach for the solid-phase synthesis of substituted cyclic guanidines, their respective bis analogues, and N-acylated guanidines from N-acylated amino acid amides [J].
Acharya, AN ;
Ostresh, JM ;
Houghten, RA .
JOURNAL OF COMBINATORIAL CHEMISTRY, 2001, 3 (06) :578-589
[3]   Solid-phase synthesis of bis-cyclic guanidines from tripeptides [J].
Acharya, AN ;
Ostresh, JM ;
Houghten, RA .
TETRAHEDRON, 2001, 57 (50) :9911-9914
[4]   A novel approach for solid-phase synthesis of substituted imidazolines and bis-imidazolines [J].
Acharya, AN ;
Ostresh, JM ;
Houghten, RA .
JOURNAL OF ORGANIC CHEMISTRY, 2001, 66 (25) :8673-8676
[5]   Tethered libraries: Solid-phase synthesis of substituted urea-linked bicyclic guanidines [J].
Acharya, AN ;
Nefzi, A ;
Ostresh, JM ;
Houghten, RA .
JOURNAL OF COMBINATORIAL CHEMISTRY, 2001, 3 (02) :189-195
[6]   Solid-phase synthesis of macrolide analogues [J].
Akritopoulou-Zanze, I ;
Sowin, TJ .
JOURNAL OF COMBINATORIAL CHEMISTRY, 2001, 3 (03) :301-311
[7]   Synthesis of a sulfahydantoin library [J].
Albericio, F ;
Bryman, LM ;
Garcia, J ;
Michelotti, EL ;
Nicolás, E ;
Tice, CM .
JOURNAL OF COMBINATORIAL CHEMISTRY, 2001, 3 (03) :290-300
[8]   An improved two-resin method for the cleavage of tertiary amines from REM resin [J].
Alhambra, C ;
Castro, J ;
Chiara, JL ;
Fernández, E ;
Fernández-Mayoralas, A ;
Fiandor, JM ;
García-Ochoa, S ;
Martín-Ortega, MD .
TETRAHEDRON LETTERS, 2001, 42 (38) :6675-6678
[9]   2-(2-oxo-1,4-dihydro-2H-quinazolin-3-yl)- and 2-(2,2-dioxo-1,4-dihydro-2H-2λ6-benzo[1,2,6]thiadiazin-3-yl)-N-hydroxy-acetamides as potent and selective peptide deformylase inhibitors [J].
Apfel, C ;
Banner, DW ;
Bur, D ;
Dietz, M ;
Hubschwerlen, C ;
Locher, H ;
Marlin, F ;
Masciadri, R ;
Pirson, W ;
Stalder, H .
JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (12) :1847-1852
[10]   A library approach to the generation of bisubstrate analogue sulfotransferase inhibitors [J].
Armstrong, JI ;
Ge, X ;
Verdugo, DE ;
Winans, KA ;
Leary, JA ;
Bertozzi, CR .
ORGANIC LETTERS, 2001, 3 (17) :2657-2660
12345678910