MECHANISM AND STEREOCHEMISTRY OF THE ENZYMIC CONVERSION OF PRENYL TO CHROMEN STRUCTURES, AS EFFECTED BY DEGUELIN CYCLASE

被引:6
作者
BHANDARI, P [1 ]
VANBRUGGEN, N [1 ]
CROMBIE, L [1 ]
WHITING, DA [1 ]
机构
[1] UNIV NOTTINGHAM,DEPT CHEM,NOTTINGHAM NG7 2RD,ENGLAND
关键词
D O I
10.1039/c39890000982
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
引用
收藏
页码:982 / 984
页数:3
相关论文
共 3 条
[1]   PROCHIRALITY TRANSFER IN THE ENZYMATIC CONVERSION OF (E)-[4'-C-13]-(6AS,12AS)-ROT-2'-ENONIC ACID INTO (6AS,12AS)-DEGUELIN - RESTRICTED STEREOSELECTIVITY IN AN ELECTRO-CYCLIZATION [J].
BEGLEY, MJ ;
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[2]   THE STEREOSPECIFIC GENERATION OF CHIRALLY LABELED BENZYLIC CENTERS IN ORTHO-PRENYLPHENOLS - 1'-R-[1'-H-3]-ROTENONIC AND 1'-S-[1'-H-3]-ROTENONIC ACID [J].
BHANDARI, P ;
CROMBIE, L ;
HARPER, MH ;
SANDERS, M ;
WHITING, DA .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1989, (15) :981-982
[3]   BIOSYNTHETIC ORIGIN OF THE 2,2-DIMETHYLCHROMEN RING - FORMATION OF DEGUELIN BY A CYCLASE ENZYME FROM TEPHROSIA-VOGELLII [J].
CROMBIE, L ;
ROSSITER, J ;
WHITING, DA .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1986, (04) :352-353