The reaction between thiols and 8-azidoadenosine derivatives.
AUTOR(ES)
Cartwright, I L
RESUMO
Thiols react at room temperature in dilute solution with 8-azidoadenosine and its nucleotides to give the corresponding 8-aminoadenosine derivatives. The reaction which takes place in the dark is base-catalysed and is particularly rapid when dithiols, e.g. dithiothreitol are used.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=343088Documentos Relacionados
- Reaction of diphenylcyclopropenone with N-acylamidine derivatives. Synthetic and mechanistic implications
- Synthesis and binding properties of conjugates between oligodeoxynucleotides and daunorubicin derivatives.
- Metabolic cooperation between mouse embryonal carcinoma cells and their differentiated derivatives.
- An investigation of a palladium catalysed biaryl synthesis of pyrrolophenanthridine derivatives. Extension of the Heck reaction
- The fundamental nature of the genetic code: prebiotic interactions between polynucleotides and polyamino acids or their derivatives.