SYNTHESIS OF A NOVEL HMG-COA REDUCTASE INHIBITOR

被引:16
作者
BAADER, E
BARTMANN, W
BECK, G
BERGMANN, A
JENDRALLA, H
KESSELER, K
WESS, G
SCHUBERT, W
GRANZER, E
VONKEREKJARTO, B
KRAUSE, R
机构
关键词
D O I
10.1016/S0040-4039(00)82484-3
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
引用
收藏
页码:929 / 930
页数:2
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共 7 条
[1]   AN EFFICIENT PREPARATION OF TRANS, TRANS-BETA-IONYLIDENEACETALDEHYDE [J].
DUGGER, RW ;
HEATHCOCK, CH .
SYNTHETIC COMMUNICATIONS, 1980, 10 (07) :509-515
[3]   STEREOSELECTIVE SYNTHESIS OF MESO(OR ERYTHRO) 1,3-DIOLS FROM BETA-HYDROXYKETONES [J].
NARASAKA, K ;
PAI, HC .
CHEMISTRY LETTERS, 1980, (11) :1415-1418
[4]  
PHILIPP BW, 1979, J LIPID RES, V20, P588
[5]   3-HYDROXY-3-METHYLGLUTARYL-COENZYME-A REDUCTASE INHIBITORS .3. 7-(3,5-DISUBSTITUTED [1,1'-BIPHENYL]-2-YL)-3,5-DIHYDROXY-6-HEPTENOIC ACIDS AND THEIR LACTONE DERIVATIVES [J].
STOKKER, GE ;
ALBERTS, AW ;
ANDERSON, PS ;
CRAGOE, EJ ;
DEANA, AA ;
GILFILLAN, JL ;
HIRSHFIELD, J ;
HOLTZ, WJ ;
HOFFMAN, WF ;
HUFF, JW ;
LEE, TJ ;
NOVELLO, FC ;
PRUGH, JD ;
ROONEY, CS ;
SMITH, RL ;
WILLARD, AK .
JOURNAL OF MEDICINAL CHEMISTRY, 1986, 29 (02) :170-181
[6]  
Therapeutic response to lovastatin (mevinolin) in nonfamilial hypercholesterolemia, 1986, JAMA, V256, P2829
[7]  
1987, DRUGS FUTURE, V12, P437