Journal
ORGANIC LETTERS
Volume 4, Issue 15, Pages 2517-2519Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol026145n
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- NIGMS NIH HHS [GM60263] Funding Source: Medline
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[GRAPHIC] The tetraacetylenic compound, (S)-minquartynoic acid (1), is synthesized in seven linear steps and 17% overall yield from commercially available azelaic acid monomethyl ester. The key step is a one-pot three-component Cadiot-Chodkiewiez reaction to construct the tetrayne unit without using either a diyne or a triyne intermediate.
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