A new and efficient solid phase synthesis of hydroxamic acids

被引:56
作者
Ngu, K [1 ]
Patel, DV [1 ]
机构
[1] VERSICOR INC,FREMONT,CA 94555
关键词
D O I
10.1021/jo971274g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[No abstract available]
引用
收藏
页码:7088 / 7089
页数:2
相关论文
共 27 条
[21]   ANGIOTENSIN-CONVERTING ENZYME-INHIBITORS - MEDICINAL CHEMISTRY AND BIOLOGICAL ACTIONS [J].
PETRILLO, EW ;
ONDETTI, MA .
MEDICINAL RESEARCH REVIEWS, 1982, 2 (01) :1-41
[22]   A TFA-cleavable linkage for solid-phase synthesis of hydroxamic acids [J].
Richter, LS ;
Desai, MC .
TETRAHEDRON LETTERS, 1997, 38 (03) :321-322
[23]   Complementarity of combinatorial chemistry and structure-based ligand design: Application to the discovery of novel inhibitors of matrix metalloproteinases [J].
Rockwell, A ;
Melden, M ;
Copeland, RA ;
Hardman, K ;
Decicco, CP ;
DeGrado, WF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (42) :10337-10338
[24]   HYDROXYUREA - A NEW TYPE OF POTENTIAL ANTITUMOR AGENT [J].
STEARNS, B ;
LOSEE, KA ;
BERNSTEIN, J .
JOURNAL OF MEDICINAL CHEMISTRY, 1963, 6 (02) :201-&
[25]   Synthesis and applications of small molecule libraries [J].
Thompson, LA ;
Ellman, JA .
CHEMICAL REVIEWS, 1996, 96 (01) :555-600
[26]   N,N,N',N'-TETRAMETHYLAZODICARBOXAMIDE (TMAD), A NEW VERSATILE REAGENT FOR MITSUNOBU REACTION - ITS APPLICATION TO SYNTHESIS OF SECONDARY-AMINES [J].
TSUNODA, T ;
OTSUKA, J ;
YAMAMIYA, Y ;
ITO, S .
CHEMISTRY LETTERS, 1994, (03) :539-542
[27]  
YOUNG CW, 1967, CANCER RES, V27, P535