Expeditious Synthesis of Mycobacterium tuberculosis Sulfolipids SL-1 and Ac(2)SGL Analogues
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Title |
Expeditious Synthesis of Mycobacterium tuberculosis Sulfolipids SL-1 and Ac(2)SGL Analogues
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Creator |
SARPE, VA
KULKARNI, SS |
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Subject |
STRAIN H37RV
ACYL CHAINS TREHALOSE ANTIGENS SULFATES |
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Description |
M. tuberculosis sulfoglycolipids SL-1 and Ac(2)SGL are highly immunogenic and potential vaccine candidates. A short and efficient methodology is reported for the synthesis of SL-1 and Ac(2)SGL analogues via regioselective functionalization of alpha,alpha-D-trehalose employing a highly regioselective late stage sulfation, as a key step. The SL-1 analogues 3a and 4 were obtained in 10 and 9 steps in 13.4% and 23.9% overall yields, respectively. The Ac(2)SGL analogue 5 was synthesized in 5 steps in 18.4% yield.
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Publisher |
AMER CHEMICAL SOC
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Date |
2014-12-28T12:52:56Z
2014-12-28T12:52:56Z 2014 |
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Type |
Article
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Identifier |
ORGANIC LETTERS, 16(21)5732-5735
1523-7060 1523-7052 http://dx.doi.org/10.1021/ol5027987 http://dspace.library.iitb.ac.in/jspui/handle/100/16615 |
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Language |
English
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