Journal of the Chemical Society. Perkin transactions I p. 377 - 382 (1996)
Update date:2022-08-05
Topics:
Ichikawa, Yoshiyasu
Kobayashi, Chie
Isobe, Minoru
A new method for the synthesis of 4-amino-D-hex-2-enopyranosides and 2-amino-D-hex-3-enopyranosides has been developed. The key feature in this method involves construction of the allylamine moiety in the pyranose framework by employing an allyl cyanate-to-isocyanate rearrangement.
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