Transprotection of N-benzoylated nucleobase derivatives by dialkylaminomethylene group

Article abstract of DOI:10.1080/07328319708002565

The use of (chloromethylene)dialkylammonium chloride in selective transprotection of N-benzoylated nucleobase derivatives is reported along with the evaluation of the stability of various protecting groups widely used in nucleoside and/or nucleotide chemi

Full text of DOI:10.1080/07328319708002565

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Nucleosides and Nucleotides
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Transprotection of N-Benzoylated
Nucleobase Derivatives by
Dialkylaminomethylene Group
Magdalena Endová a , Milena Masojidková a & Ivan Rosenberg a
a Institute of Organic Chemistry and Biochemistry, Academy of
Sciences of the Czech Republic , Flemingovo nám. 2, 166 10, Prague,
6, Czech Republic
Published online: 23 Aug 2006.
To cite this article: Magdalena Endová , Milena Masojidková & Ivan Rosenberg (1997) Transprotection
of N-Benzoylated Nucleobase Derivatives by Dialkylaminomethylene Group, Nucleosides and
Nucleotides, 16:12, 2151-2164, DOI: 10.1080/07328319708002565
To link to this article: http://dx.doi.org/10.1080/07328319708002565
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