
Carbohydrate Research p. 5 - 24 (1982)
Update date:2022-07-31
Topics: Enantiomer Stereoselective synthesis Protecting group Chiral synthesis Macrolide erythronolide A Diastereomer Benzyl ether
Kinoshita, Mitsuhiro
Ohsawa, Naoki
Gomi, Shuichi
3,6-Dideoxy-1,2-O-isopropylidene-3-C-methyl-α-D-glucofuranose (9) was prepared from methyl 4,6-O-benzylidene-3-deoxy-3-C-methyl-α-D-glucopyranoside via 3-deoxy-1,2-O-isopropylidene-3-C-methyl-α-D-glucofuranose (5) in 61percent yield.The key intermediates,
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Doi:10.1055/s-1982-29963
(1982)Doi:10.1021/jm00364a004
(1983)Doi:10.14233/ajchem.2013.14048
(2013)Doi:10.1016/j.jorganchem.2007.01.046
(2007)Doi:10.1039/b008520k
(2001)Doi:10.1002/anie.201808352
(2018)