| Literature DB >> 18696363 |
Nadia L D Cabral1, Luciano Hoeltgebaum Thiessen, Bogdan Doboszewski.
Abstract
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.Entities:
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Year: 2008 PMID: 18696363 DOI: 10.1080/15257770802257846
Source DB: PubMed Journal: Nucleosides Nucleotides Nucleic Acids ISSN: 1525-7770 Impact factor: 1.381