REACTION OF BENZENESELENENYL HALIDES WITH ESTROGENS

被引:16
作者
ALI, H [1 ]
VANLIER, JE [1 ]
机构
[1] UNIV SHERBROOKE,FAC MED,MRC,RADIAT SCI GRP,SHERBROOKE J1H 5N4,QUEBEC,CANADA
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1991年 / 02期
关键词
D O I
10.1039/p19910000269
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The reaction of estradiol and estrone with benzeneselenenyl chloride affords mainly 2-phenylselenenyl adducts which are readily converted into the corresponding 2-halogenated estrogens upon treatment with a variety of reagents.
引用
收藏
页码:269 / 271
页数:3
相关论文
共 12 条
[1]   REGIOSELECTIVE A-RING IODINATION OF ESTRADIOL DIACETATES [J].
ALI, H ;
GHAFFARI, MA ;
VANLIER, JE .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1987, 28 (01) :21-23
[2]   PHSECL AS A CHLORINATING AGENT FOR ACTIVATED BENZENE-DERIVATIVES [J].
AYORINDE, FO .
TETRAHEDRON LETTERS, 1983, 24 (20) :2077-2078
[3]   CLAY-SUPPORTED REAGENTS .5. NITRATION OF ESTRONE INTO 2-NITROESTRONE BY CLAY-SUPPORTED FERRIC NITRATE [J].
CORNELIS, A ;
LASZLO, P ;
PENNETREAU, P .
JOURNAL OF ORGANIC CHEMISTRY, 1983, 48 (24) :4771-4772
[4]   NOVEL REGIOSELECTIVE IODINATION OF ESTRADIOL 17-BETA-ACETATE [J].
HORIUCHI, CA ;
HAGA, A ;
SATOH, JY .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1986, 59 (08) :2459-2462
[5]  
PAGE PCB, 1990, TETRAHEDRON, V46, P2059
[6]   AN ALTERNATIVE ROUTE TO 2-BROMO-ESTRADIOLS AND 2-IODO-ESTRADIOLS FROM ESTRADIOL [J].
PERT, DJ ;
RIDLEY, DD .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1987, 40 (02) :303-309
[7]   A-RING NITRATION OF ESTRONE [J].
SANTANIELLO, E ;
RAVASI, M ;
FERRABOSCHI, P .
JOURNAL OF ORGANIC CHEMISTRY, 1983, 48 (05) :739-740
[8]  
SANTANIELLO E, 1983, J CHEM SOC PERK T 1, P2765, DOI 10.1039/p19830002765
[9]   A-RING IODINATION OF ESTRADIOL [J].
SWEET, F ;
PATRICK, TB ;
MUDD, JM .
JOURNAL OF ORGANIC CHEMISTRY, 1979, 44 (13) :2296-2298
[10]  
THOMSON AJ, 1959, J ORG CHEM, V24, P2056