Towards a general solid phase approach for the iterative synthesis of conjugated oligomers using a germanium based linker - first solid phase synthesis of an oligo-(triarylamine)

2007 ◽  
Vol 5 (11) ◽  
pp. 1752-1763 ◽  
Author(s):  
David J. Turner ◽  
Rémi Anémian ◽  
Philip R. Mackie ◽  
Domenico C. Cupertino ◽  
Stephen G. Yeates ◽  
...  
RSC Advances ◽  
2018 ◽  
Vol 8 (6) ◽  
pp. 3343-3347 ◽  
Author(s):  
Blake E. Daniels ◽  
Craig E. Stivala

A solid-phase synthesis of α-aminoboronic acid peptides using a 1-glycerol polystyrene resin is described.


2015 ◽  
Vol 6 (7) ◽  
pp. 4131-4140 ◽  
Author(s):  
Andrei Loas ◽  
Robert J. Radford ◽  
Alexandria Deliz Liang ◽  
Stephen J. Lippard

A synthetically facile solid-phase approach yields fluorescent Cu(ii)-based lysine conjugates which selectively detect nitroxyl and thiols in live cells.


2003 ◽  
Vol 771 ◽  
Author(s):  
D. Turner ◽  
A. Spivey ◽  
D. Cupertino ◽  
P. Mackie ◽  
R. Anemian ◽  
...  

AbstractA new solid phase synthetic strategy for the production of organic semiconductors has been developed. The strategy uses a germanium-based linker and Suzuki-type cross-coupling protocols and has been demonstrated for the iterative synthesis of both a regio-regular oligo-3-alkyl-thiophene and an oligoarylamine. The process also incorporates a novel “doublecoupling” after each iteration which minimizes deletion sequences. The key steps exploits the susceptibility of α-silyl- or α-silyloxy- but not germyl-substituted derivatives toward nucleophilic ipso-protodemetalation.


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