Chlorination of 1,5-Anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-arabino-hex-1-enitol; Highly Stereoselective Preparation of α-D-Glucopyranosyl Chloride and ω-Chloroalkyl β-D-Glucopyranosides

DOI: 10.1039/c39830000449

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 449 - 450 (1983)

Update date:2022-08-03

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Authors:

Sakakibara, Tohru

Nomura, Yutaka

Yoshino, Kohji

Sudoh, Rokuro

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Article abstract of DOI:10.1039/c39830000449

Chlorination of 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-arabino-hex-1-enitol in cyclic ethers such as tetrahydrofuran stereoselectively afforded the ω-chloroalkyl β-D-glucopyranoside derivatives, whereas in 1,4-dioxane α-D-glucopyranosyl chlor

Full text of DOI:10.1039/c39830000449

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