CHEMISTRY OF ARYLLEAD(IV) TRICARBOXYLATES - REACTION WITH BETA-KETO-ESTERS - CONVENIENT ROUTE TO ALPHA-ARYLATED KETONES

被引:58
作者
PINHEY, JT
ROWE, BA
机构
关键词
D O I
10.1071/CH9800113
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
引用
收藏
页码:113 / 120
页数:8
相关论文
共 24 条
[1]  
ALADEL I, 1976, B SOC CHIM FR II-CH, P930
[2]  
AVELA E, 1956, ANN ACAD SCI FENN, V77, P84
[3]  
BELL H, UNPUBLISHED
[4]   CHEMISTRY OF ARYLLEAD(IV) TRICARBOXYLATES - REACTION WITH PHENOLS [J].
BELL, HC ;
PINHEY, JT ;
STERNHELL, S .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1979, 32 (07) :1551-1560
[5]  
BELL HC, 1976, TETRAHEDRON LETT, P4303
[6]   CHEMISTRY OF ARYLLEAD(IV) TRICARBOXYLATES - REACTION WITH AROMATICS TO GIVE BIARYLS [J].
BELL, HC ;
KALMAN, JR ;
MAY, GL ;
PINHEY, JT ;
STERNHELL, S .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1979, 32 (07) :1531-1550
[7]   CHEMISTRY OF ARYLLEAD(IV) TRICARBOXYLATES - SYNTHESIS [J].
BELL, HC ;
KALMAN, JR ;
PINHEY, JT ;
STERNHELL, S .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1979, 32 (07) :1521-1530
[8]  
BELL HC, 1974, TETRAHEDRON LETT, P857
[9]   PHOTOSTIMULATED ARYLATION OF KETONE ENOLATE IONS BY SRN1 MECHANISM [J].
BUNNETT, JF ;
SUNDBERG, JE .
JOURNAL OF ORGANIC CHEMISTRY, 1976, 41 (10) :1702-1706
[10]   DIE PRAPARATIVE BEDEUTUNG DER ZERSETZUNG VON DIAZO-CARBONYLVERBINDUNGEN IM UV-LICHT [J].
HORNER, L ;
SPIETSCHKA, E .
CHEMISCHE BERICHTE-RECUEIL, 1952, 85 (03) :225-229