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Substituted homoallenyl aldehydes and their derivatives. Part 1: Homoallenyl aldehydes and protected hydrazones
Autoři | |
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Rok publikování | 2013 |
Druh | Článek v odborném periodiku |
Časopis / Zdroj | Chemical Papers |
Fakulta / Pracoviště MU | |
Citace | |
www | http://www.springerlink.com/content/bg530413q7034142/ |
Doi | http://dx.doi.org/10.2478/s11696-012-0215-6 |
Obor | Organická chemie |
Klíčová slova | homoallenyl aldehyde; hydrazone; Claisen rearrangement; isomerisation |
Popis | The paper presents a simple synthesis of substituted propargyl vinyl ethers and their subsequent thermally-initiated Claisen rearrangement leading to various 3-substituted homoallenyl aldehydes. Several methods, including Sonogashira coupling, base-promoted substitution on the triple bond by sodium amide or butyllithium, and the preparation of substituted propargyl alcohols, were used in the initial step. Phosphate-protected homoallenyl aldehyde hydrazone derivatives were synthesised and fully characterised. The stereochemistry of 9-anthracene carbaldehyde hydrazone, which, surprisingly, afforded both cis and trans isomers, was established using X-ray analysis. |
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