2,3-PYRIDINE ANNULATION - THE ENANTIOSELECTIVE SYNTHESIS OF AN ALDOSE REDUCTASE INHIBITOR

被引:12
作者
MURTIASHAW, CW
BREITENBACH, R
GOLDSTEIN, SW
PEZZULLO, SL
QUALLICH, GJ
SARGES, R
机构
[1] Process R & D, Central Research Division, Pfizer, Inc., Connecticut 06340, Eastern Point Road, Groton
关键词
D O I
10.1021/jo00032a060
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:1930 / 1933
页数:4
相关论文
共 9 条
[1]   3,4-DIHYDRO-2-PHENYL-2H-PYRANO[2,3-B]PYRIDINES WITH POTENT ANTIRHINOVIRUS ACTIVITY [J].
BARGAR, TM ;
DULWORTH, JK ;
KENNY, MT ;
MASSAD, R ;
DANIEL, JK ;
WILSON, T ;
SARGENT, RN .
JOURNAL OF MEDICINAL CHEMISTRY, 1986, 29 (09) :1590-1595
[2]   A DRAMATIC SOLVENT EFFECT DURING AROMATIC HALOGEN METAL EXCHANGES - DIFFERENT PRODUCTS FROM LITHIATION OF POLYFLUOROBROMOBENZENES IN ETHER AND THF [J].
BRIDGES, AJ ;
PATT, WC ;
STICKNEY, TM .
JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (02) :773-775
[3]   THE DEVELOPMENT AND USE OF QUANTUM-MECHANICAL MOLECULAR-MODELS .76. AM1 - A NEW GENERAL-PURPOSE QUANTUM-MECHANICAL MOLECULAR-MODEL [J].
DEWAR, MJS ;
ZOEBISCH, EG ;
HEALY, EF ;
STEWART, JJP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (13) :3902-3909
[4]   REGIOSELECTIVE ORTHO LITHIATION OF HALOPYRIDINES [J].
GRIBBLE, GW ;
SAULNIER, MG .
TETRAHEDRON LETTERS, 1980, 21 (43) :4137-4140
[5]   ENANTIOMERICALLY PURE SYNTHETIC BUILDING-BLOCKS WITH 4 C-ATOMS AND 2 OR 3 FUNCTIONAL-GROUPS FROM BETA-HYDROXY-BUTANOIC, MALIC, AND TARTARIC ACID [J].
HUNGERBUHLER, E ;
SEEBACH, D ;
WASMUTH, D .
HELVETICA CHIMICA ACTA, 1981, 64 (05) :1467-1487
[6]   NEW REACTIONS OF HALOPYRIDINES WITH BUTYLLITHIUM - PROPOSED MECHANISM OF METALATION AND BROMINE MIGRATION [J].
MALLET, M ;
QUEGUINER, G .
TETRAHEDRON, 1979, 35 (13) :1625-1631
[7]   NUCLEAR MAGNETIC-RESONANCE DETERMINATION OF ENANTIOMERIC COMPOSITION AND ABSOLUTE-CONFIGURATION OF GAMMA-LACTONES USING CHIRAL 2,2,2-TRIFLUORO-1-(9-ANTHRYL)ETHANOL [J].
PIRKLE, WH ;
SIKKENGA, DL ;
PAVLIN, MS .
JOURNAL OF ORGANIC CHEMISTRY, 1977, 42 (02) :384-387
[8]   SPIRO HYDANTOIN ALDOSE REDUCTASE INHIBITORS DERIVED FROM 8-AZA-4-CHROMANONES [J].
SARGES, R ;
GOLDSTEIN, SW ;
WELCH, WM ;
SWINDELL, AC ;
SIEGEL, TW ;
BEYER, TA .
JOURNAL OF MEDICINAL CHEMISTRY, 1990, 33 (07) :1859-1865
[9]  
SARGES R, 1986, METABOLISM S1, V35, P104