A simplified procedure for the preparation of 2,3-O-isopropylidene-sn-glycerol from L-arabinose.
A new procedure for the preparation of 2,3-O-isopropylidene-sn-glycerol is described. L-arabinose is converted to its 4,5-monoisopropylidene diethyl mercaptal derivative. This compound is then subjected to periodate oxidation and borohydride reduction. Following neutralization, the aceton-glycerol i...
Main Authors: | P Kanda, M A Wells |
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Format: | Article |
Language: | English |
Published: |
Elsevier
1980-02-01
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Series: | Journal of Lipid Research |
Online Access: | http://www.sciencedirect.com/science/article/pii/S0022227520398321 |
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