The Barbier–Wieland degradation is a procedure for shortening the carbon chain of a carboxylic acid by one carbon. It only works when the carbon adjacent to the carboxyl is a simple methylene bridge (an aliphatic carbon with no substituents). The reaction sequence involves conversion of the carboxyl and alpha carbon into an alkene, which is then cleaved by oxidation to convert the former alpha position into a carboxyl itself.[1][2]
References
edit- ^ Byron Riegel, Byron; Moffett, R. B.; McIntosh A. V. (1955). "nor-Desoxycholic Acid". Organic Syntheses. 24: 38; Collected Volumes, vol. 3, p. 234.
- ^ Byron Riegel, Byron; Moffett, R. B.; McIntosh A. V. (1955). "3,12-Diacetoxy-bisnor-cholanyldiphenylethylene". Organic Syntheses. 24: 41; Collected Volumes, vol. 3, p. 237.
 | This organic chemistry article is a stub. You can help Wikipedia by expanding it. |