
Carbohydrate Research p. 369 - 374 (1985)
Update date:2022-08-04
Topics:
Lancelin, Jean-Marc
Pougny, Jean-Rene
Sinay, Pierre
3,4,5,7-Tetra-O-benzyl-D-gluco-hept-1-enitol was submitted to a selenocyclisation-oxidation-elimination sequence to provide 2,6-anhydro-3,4,5,7-tetra-O-benzyl-1-deoxy-D-gluco-hept-1-enitol in 54percent yield.Treatment of methyl 2,3,4-tri-O-benzyl-α-D-gluc
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(2005)Doi:10.1016/j.bmcl.2020.127247
(2020)