Preparation of 2,3-Dideoxy-2,3-epimino and 3,4-Dideoxy-3,4-epimino Derivatives of 1,6-Anhydro-β-D-hexopyranoses by Mitsunobu Reaction
1998 ◽
Vol 63
(6)
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pp. 813-825
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A series of new 2-, 3- and 4-benzylamino-2-, 3- and 4-deoxy derivatives of 1,6-anhydro-β-D-hexopyranoses were prepared from 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses by treatment with benzylamine and converted into 2,3-(N-benzylepimino)-2,3-dideoxy- and 3,4-(N-benzylepimino)-3,4-dideoxy-β-D-hexopyranoses of the D-allo, D-galacto and D-talo configuration by Mitsunobu reaction. The structures of benzylamino and benzylimino derivatives were confirmed by 1H and 13C NMR spectra.
1989 ◽
Vol 54
(3)
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pp. 713-724
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2018 ◽
Vol 19
(2)
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pp. 113-117
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1991 ◽
Vol 56
(12)
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pp. 2969-2977
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1987 ◽
Vol 52
(6)
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pp. 1494-1500
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1984 ◽
Vol 49
(12)
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pp. 2897-2902
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1980 ◽
Vol 45
(10)
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pp. 2772-2778
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