Propargyloxycarbonyl (Poc) as a Protective Group for the Hydroxyl Function in Carbohydrate Synthesis
The propargyloxycarbonyl (Poc) group can be used for the selective protection of the hydroxyl function in carbohydrates and can be removed under neutral conditions using tetrathiomolybdate MoS4 2- (1) in CH3CN at room temperature. Under the conditions of deprotection benzylidine acetals, benzyl ethe...
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Veröffentlicht in: | Organic letters 2002-12, Vol.4 (26), p.4731-4733 |
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creator | Sridhar, Perali Ramu Chandrasekaran, S |
description | The propargyloxycarbonyl (Poc) group can be used for the selective protection of the hydroxyl function in carbohydrates and can be removed under neutral conditions using tetrathiomolybdate MoS4 2- (1) in CH3CN at room temperature. Under the conditions of deprotection benzylidine acetals, benzyl ethers, acetyl and levulinoyl esters, and allyl and benzyl carbonates are left untouched. It has also been shown that the new protective group (Poc) is compatible with acidic, basic, and also glycosylation conditions. |
doi_str_mv | 10.1021/ol027220x |
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title | Propargyloxycarbonyl (Poc) as a Protective Group for the Hydroxyl Function in Carbohydrate Synthesis |
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