Abstract
Acetylation of D-mannose phenylhydrazone gives acetylated
D-arabino-1-phenyl-azo-1-(E)-hexene. Subsequent reduction with
sodium borohydride produces 2-deoxy-D-arabino-hexose
phenylhydrazone which, on hydrolysis, gives
2-deoxy-D-arabino-hexose. By a similar procedure
2-deoxy-D-lyxo-hexose, 2,6-dideoxy-L-arabino-hexose, and
2-deoxy-D-erythropentose can be prepared from D-galactose,
L-rhamnose, and D-arabinose, respectively.
Original language | English |
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Journal | Carbohydrate Research |
Volume | 199 |
Pages (from-to) | 307-310 |
ISSN | 0008-6215 |
Publication status | Published - 1997 |