Please use this identifier to cite or link to this item: http://hdl.handle.net/10497/17653
Title: 
Absolute stereochemistry of the β-hydroxy acid unit in hantupeptins and trungapeptins
Authors: 
Keywords: 
β-hydroxy acid
Hantupeptins
Trungapeptins
Depsipeptides
Marine cyanobacterium
Mosher’s reagent
Issue Date: 
2015
Citation: 
Gupta, D. K., Chi, G. Y. D., Teo, Y. C., & Tan, L. T. (2015). Absolute stereochemistry of the β-hydroxy acid unit in hantupeptins and trungapeptins. Natural Product Communications, 11, 1-4.
Abstract: 
Theβ-hydroxyl amino acid unit is a common structural feature of many bioactive marine cyanobacterial depsipeptides. In this study, the absolute stereochemistry of the β-hydroxyl acid moieties in hantupeptins and trungapeptins were determined through their synthesis and HPLC analysis of the Mosher ester derivatives. Synthesis of two3-hydroxy-2-methyloctanoic acid (Hmoa) stereoisomers, (2S,3R)-Hmoa and (2S,3S)-Hmoa, were achieved using diastereoselective asymmetric method and the retention times of all four Hmoa isomers were established indirectly by RPLC-MS analysis of their Mosher ester derivative standards. Based on the retention times of the standards, the absolute configuration of the Hmoa unit in hantupeptin C (3) and trungapeptin C (6) was assigned as (2R,3S)- and (2S,3R)-Hmoa, respectively. The use of the Mosher's reagents, coupled with HPLC analysis, provided a viable alternative to the absolute stereochemical determination of -hydroxy acid units in depsipeptides.
URI: 
ISSN: 
1934-578X (print)
1555-9475 (online)
Appears in Collections:Journal Articles

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