Stereochemistry of Nucleophilic Addition Reactions. VIII. Preparation of 1,5-Anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-erythro-hex-2-enitol and Its Reactions with Some Nucleophiles

DOI: 10.1246/bcsj.53.1642

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Bulletin of the Chemical Society of Japan p. 1642 - 1646 (1980)

Update date:2022-08-05

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Authors:

Sakakibara, Tohru

Nomura, Yutaka

Sudoh, Rokuro

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Article abstract of DOI:10.1246/bcsj.53.1642

The title compound was synthesized from 1,5-anhydro-D-glucitol via nitromethane cyclization.The reduction of the compound with sodium borodeuteride afforded a mixture of saturated nitro compounds having an axial and equatorial deuterium atom at C-2 in an

Full text of DOI:10.1246/bcsj.53.1642

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