THE MICHAEL REACTION OF A METHYL 2-C-NITRO-α-D-HEX-2-ENOPYRANOSIDE: PREPARATIONAND STUCTURAL DETERMINATION OF THE ADDUCTS HAVING THE D-altro-, D-gluco- AND D-manno CONFIGURATIONS

DOI: 10.1016/S0008-6215(00)80992-1

Source and publish data:

Carbohydrate Research p. 67 - 76 (1981)

Update date:2022-09-26

Topics:

Authors:

Sakakibara, Tohru

Tachimori, Yoshifusa

Minami, Toshiaka

Sudoh, Rokuro

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Article abstract of DOI:10.1016/S0008-6215(00)80992-1

The reaction of methyl 4,6-O-benzylidene-2,3-dideoxy-2-C-nitro-α-D-erythro-hex-2-enopyranoside (1) with 2,4-pentanedione and diethyl malonate afforded adducts having the D-altro-, D-gluco- and D-manno configurations.Besides the adducts having the D-gluco-

Full text of DOI:10.1016/S0008-6215(00)80992-1

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