(π-Allyl)palladium coupling of 2-(tributylstannyl)cyclopent-2-enone for the synthesis of jasmonoid analogs

2017 ◽  
Vol 58 (20) ◽  
pp. 1965-1968
Author(s):  
Florencia Parpal ◽  
Enrique Pandolfi ◽  
Viviana Heguaburu
Keyword(s):  
1994 ◽  
Vol 35 (27) ◽  
pp. 4711-4714 ◽  
Author(s):  
Miguel A. Romero ◽  
Alex G. Fallis
Keyword(s):  

Synthesis ◽  
2010 ◽  
Vol 2011 (03) ◽  
pp. 480-484
Author(s):  
Pascal Carato ◽  
Céline Pirat ◽  
Vincent Ultré ◽  
Nicolas Lebegue ◽  
Pascal Berthelot ◽  
...  

1999 ◽  
Vol 11 (10) ◽  
pp. 2974-2983 ◽  
Author(s):  
Richard W. Wagner ◽  
Yangzhen Ciringh ◽  
Christian Clausen ◽  
Jonathan S. Lindsey

2001 ◽  
Vol 79 (11) ◽  
pp. 1827-1839 ◽  
Author(s):  
Léon Ghosez ◽  
Cécile Franc ◽  
Frédéric Denonne ◽  
Claire Cuisinier ◽  
Roland Touillaux

Suzuki cross-coupling reactions of 3-pyrroleboronic acid derivatives with haloaromatics and the reverse process i.e., the coupling of 3-iodo(bromo)pyrroles with arylboronic acids have been investigated as a potential key step in the synthesis of (–)-rhazinilam and analogues. It was found that 3-iodo-2-formyl-1-tosylpyrroles efficiently coupled with a variety of arylboronic acids in the presence of PdCl2(dppf) as catalyst. This catalytic system is compatible with a broad spectrum of arylboronic acids — electron-rich, electron-poor, hindered, heterocyclic — which easily coupled with the pyrrole substrate.Key words: 2-substituted-3-arylpyrroles, biaryls, coupling reactions, arylboronic acids, palladium coupling, catalysis.


2002 ◽  
Vol 80 (6) ◽  
pp. 646-652 ◽  
Author(s):  
Daniel R Sidler ◽  
Nancy Barta ◽  
Wenjie Li ◽  
Essa Hu ◽  
Louis Matty ◽  
...  

The convergent synthesis of a potent α1A-selective adrenoceptor antagonist is described. Salient features of the synthesis include the enzymatic resolution of a racemic dihydropyrimidinone and the use of a palladium coupling reaction in the synthesis of 2,4'-dipyridyl.Key words: dihydropyrimidinone, enzymatic resolution, palladium coupling.


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