scholarly journals Synthesis of diverse indole libraries on polystyrene resin – Scope and limitations of an organometallic reaction on solid supports

2012 ◽  
Vol 8 ◽  
pp. 1191-1199 ◽  
Author(s):  
Kerstin Knepper ◽  
Sylvia Vanderheiden ◽  
Stefan Bräse

The synthesis of diverse substituted indole structures on solid supports is described. The immobilization of nitrobenzoic acid onto Merrifield resin and the subsequent treatment with alkenyl Grignard reagents delivered indole carboxylates bound to solid supports. In contrast to results in the liquid phase, ortho,ortho-unsubstituted nitroarenes also delivered indole moieties in good yields. Subsequent palladium-catalyzed reactions (Suzuki, Heck, Sonogashira, Stille) delivered, after cleavage, the desired molecules in moderate to good yields over four steps. The scope and limitations are presented.

2006 ◽  
Vol 2006 (8) ◽  
pp. 1886-1898 ◽  
Author(s):  
Kerstin Knepper ◽  
Sylvia Vanderheiden ◽  
Stefan Bräse

Synlett ◽  
1993 ◽  
Vol 1993 (09) ◽  
pp. 680-682 ◽  
Author(s):  
Jean Pierre Genêt ◽  
Errol Blart ◽  
Monique Savignac ◽  
Stéphane Lemeune ◽  
Sandrine Lemaire-Audoire ◽  
...  

2009 ◽  
Vol 62 (1) ◽  
pp. 27 ◽  
Author(s):  
Vaibhav P. Mehta ◽  
Sachin G. Modha ◽  
Denis Ermolat'ev ◽  
Kristof Van Hecke ◽  
Luc Van Meervelt ◽  
...  

A highly efficient method for the synthesis of diversely substituted furo[2,3-b]pyrazines has been elaborated. The Ag+- or iodine-mediated electrophilic cyclization of readily generated 5-chloro-3-substituted ethynyl-1-(4-methoxybenzyl)-pyrazin-2(1H)-ones affords substituted furo[2,3-b]pyrazines, which undergo various palladium catalyzed reactions to generate a library of difficult to attain diversely substituted furo[2,3-b]pyrazines.


Sign in / Sign up

Export Citation Format

Share Document