13444-15-0Relevant articles and documents
An unusually facile [3,3]-sigmatropic rearrangement in a stereospecific synthesis of novel 2′,3′-dideoxynucleoside precursors
Armstrong, Peter L.,Coull, Lain C.,Hewson, Alan T.,Slater, Martin J.
, p. 4311 - 4314 (1995)
The glycal 5 is converted to intermediates which undergo, under mild conditions, thermal aza-Claisen rearrangements, leading to the amides 7 and 8 and the 2-pyrimidone 9, all potential precursors to 2′,3′-dideoxynucleosides.