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The reaction of alkyllithium reagents with Furan-3-carboxylic acid. A synthesis of 4-(Furan-3'-yl)-1-methylbutyltriphenylphosphonium iodide

E Dimitriadis and RA Massy-Westropp
37(3) pp.619 - 627


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Enantioselective Total Synthesis and Determination of the Absolute Configuration of the 4,6,8,10,16,18‐Hexamethyldocosane from Antitrogus parvulus
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ChemInform Abstract: THE REACTION OF ALKYLLITHIUM REAGENTS WITH FURAN‐3‐CARBOXYLIC ACID. A SYNTHESIS OF 4‐(FURAN‐3′‐YL)‐1‐METHYLBUTYLTRIPHENYLPHOSPHONIUM IODIDE
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Hypervalent (tert-Butylperoxy)iodanes Generate Iodine-Centered Radicals at Room Temperature in Solution:  Oxidation and Deprotection of Benzyl and Allyl Ethers, and Evidence for Generation of α-Oxy Carbon Radicals
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Enantioselective Total Synthesis and Determination of the Absolute Configuration of the 4,6,8,10,16,18‐Hexamethyldocosane from Antitrogus parvulus
Herber Christian, Breit Bernhard
Angewandte Chemie International Edition. 2005 44(33). p.5267
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Chemical Reviews. 2009 109(9). p.3903

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