89647-11-0Relevant articles and documents
SYNTHESE DE NUCLEOSIDES SUBSTITUES EN C-5 PAR UN CARBOCYCLE OU UN HETEROCYCLE PAR COUPLAGES D'ORGANOZINCIQUES AVEC L'IODO-5 O-BIS(TRIMETHYLSILYL)-3',5'DESOXY-2' URIDINE CATALYSES PAR DES COMPLEXES ORGANOPALLADIES
Vincent, P.,Beaucourt, J. P.,Pichat, L.
, p. 201 - 202 (1984)
Some nucleosides, substituted at C-5 by a carbocycle or an heterocycle,were obtained in low yields by the palladium-catalyzed reaction of organozinc reagents with O-3' ,5' bis (trimethylsilyl)-2'-desoxyuridine
New water soluble Pd-imidate complexes as highly efficient catalysts for the synthesis of C5-arylated pyrimidine nucleosides
Kapdi, Anant,Gayakhe, Vijay,Sanghvi, Yogesh S.,Garcia, Joaquin,Lozano, Pedro,Da Silva, Ivan,Perez, Jose,Serrano, J. Luis
, p. 17567 - 17572 (2014/05/06)
The direct reactions between the precursors trans-[Pd(imidate) 2(SMe2)2] and 1,3,5-triaza-7-phosphaadamantane (PTA) yield new water-soluble palladium(ii) complexes trans-[Pd(imidate) 2(PTA)2](imidate
New, efficient approach for the ligand-free Suzuki-Miyaura reaction of 5-iodo-2′-deoxyuridine in water
Sartori, Guillaume,Herve, Gwenaelle,Enderlin, Gerald,Len, Christophe
, p. 330 - 333 (2013/03/14)
A series of 5-aryl-2′-deoxyuridines was prepared, using ligandless Suzuki-Miyaura cross-coupling reactions in neat water, starting from 5-iodo-2′-deoxyuridine as totally deprotected starting material. This ligand-free process gave good to high isolated yi
