Total synthesis of violaceimides A-E and consideration of the reported stereochemistry

被引:0
|
作者
Perry, Charles K. [2 ]
Fulton, Mark G. [1 ]
Lindsley, Craig W. [1 ,2 ]
机构
[1] Vanderbilt Univ, Dept Chem, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Vanderbilt Ctr Neurosci Drug Discovery, Dept Pharmacol, Nashville, TN 37232 USA
关键词
Violaceimide; Enantioselective; Total synthesis; Natural product;
D O I
10.1016/j.tetlet.2019.151103
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Here we report the first total synthesis of violaceimides A-E, a family of sulfur-containing metabolites from Aspergillus violaceus, a sponge-associated fungus. A concise, convergent and enantioselective synthesis was developed for all five family members, from a common advanced intermediate. However, while the NMR spectral data matched that of the reported natural products, the optical rotations were of opposite sign. This result prompted the enantioselective synthesis of all four diastereomeric pairs of violaceimide E, and suggests that the stereochemistry might have been misassigned. (C) 2019 Elsevier Ltd. All rights reserved.
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页数:4
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