
Carbohydrate Research p. 271 - 278 (1992)
Update date:2022-08-05
Topics:
Sakakibara
Takaide
Seta
Irradiation of 3-nitro-2-enopyranoside derivatives having α-D-erythro, β-D-threo, and α-D-threo configurations in 1,3-dioxolane afforded adducts in moderate yields. Structural assignment of the adducts, including conformational analyses of the 1,3-dioxolanyl moiety, were performed. Irradiation of 3-nitro-2-enopyranoside derivatives having α-D-erythro, β-D-threo, and α-D-threo configurations in 1,3-dioxolane afforded adducts in moderate yields. Structural assignment of the adducts, including conformational analyses of the 1,3-dioxolanyl moiety, were performed.
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Doi:10.1039/c2ob27070f
(2013)Doi:10.1246/bcsj.65.1052
(1992)Doi:10.1002/ejic.201402662
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(2012)Doi:10.1002/ejic.201200560
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(1972)