79607-52-6Relevant academic research and scientific papers
TRANSFORMATION OF HEX-2-ENOPYRANOSYL TRICHLOROACETIMIDATES - A CORRECTION
Dyong, Ingolf,Merten, Hans,Thiem, Joachim
, p. 277 - 280 (1984)
Contrary to previous results hex-2-enopyranosyl trichloroacetimidates do not rearrange to amino-branched glycals but give N-acylated hex-2-enopyranosyl amines.
UNVERZWEIGTE UND R-C-N-VERZWEIGTE AMINOZUCKER DURCH TRICHLORACETIMIDAT-UMLAGERUNG
Dyong, Ingolf,Weigand, Joachim,Merten, Hans
, p. 2965 - 2968 (2007/10/02)
Trichloroacetimidates from carbohydrates with an endo- or an exocyclic allylic alcohol grouping rearrange under thermal conditions with formation of unbranched or R-C-N branched amino sugars.
