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Nucleosides Nucleotides Nucleic Acids ; 27(8): 931-48, 2008 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-18696363

RESUMO

The triphenylmethyl (Tr) group undergoes a transfer (transetherification or disproportionation) between the molecules of 5'-O-Tr-2'-deoxynucleosides in a process mediated by anhydrous sulfates of Cu(+2), Fe(+2), or Ni(+2) to yield mixtures of 3',5'-bis-O-Tr and 3'-O-Tr products. If phenylmethanol is present in a reaction medium, detritylation results with concomitant formation of phenylmethyl triphenylmethyl ether. The behavior of t-butyldimethylsilyl (TBDMS) group in 5'-O-TBDMS-2'-deoxynucleosides is exactly the same. Such type of transetherifications was not observed before for the O-Tr and O-TBDMS groups.


Assuntos
Química Orgânica/métodos , Nucleosídeos/química , Siloxanas/química , Estirenos/química , Compostos de Tritil/química , Sulfato de Cálcio/química , Estrutura Molecular
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