
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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(1972)