4.7 Article

Synthesis of the 1,2,4-Thiadiazole Alkaloid Polyaurine B

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 83, Issue 5, Pages 1721-1724

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.0c00166

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Funding

  1. University of Auckland

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A short synthesis of the natural product polyaurine B is described. The 1,2,4-thiadiazole heterocycle was assembled using a Cu(II)-mediated heterocyclization reaction that forges the N-S bond. The final acylation step to install the methylcarbamate must be conducted under anhydrous, nonbasic conditions to prevent thiadiazole ring opening initiated by attack of hydroxide at C-5.

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