O-substituted alkyl aldehydes for rhodium-catalyzed intermolecular alkyne hydroacylation: the utility of methylthiomethyl ethers.
Combining α-methylthiomethyl (MTM) ether substituted aldehydes and 1-alkynes in the presence of [Rh(dppe)]ClO(4) results in efficient intermolecular alkyne hydroacylation to deliver α-O-MTM-substituted enone products. The product MTM ethers can be converted to the free hydroxyl group either in situ,...
主要な著者: | Parsons, SR, Hooper, J, Willis, M |
---|---|
フォーマット: | Journal article |
言語: | English |
出版事項: |
2011
|
類似資料
-
Traceless chelation-controlled rhodium-catalyzed intermolecular alkene and alkyne hydroacylation.
著者:: Hooper, J, 等
出版事項: (2013) -
Rhodium-catalyzed intermolecular chelation controlled alkene and alkyne hydroacylation: synthetic scope of beta-S-substituted aldehyde substrates.
著者:: Willis, M, 等
出版事項: (2006) -
Rhodium (I) catalyzed intermolecular hydroacylation.
著者:: Sapmaz, S, 等
出版事項: (2001) -
Rhodium-catalysed intermolecular alkyne hydroacylation: the enantioselective synthesis of α- and β-substituted ketones by kinetic resolution.
著者:: González-Rodríguez, C, 等
出版事項: (2010) -
Exploiting carbonyl groups to control intermolecular rhodium-catalyzed alkene and alkyne hydroacylation
著者:: Coxon, TJ, 等
出版事項: (2017)