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ChemInform 2010, 41, issue 07 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Aldehydes Q 0320 DOI: 10.1002/chin.201007064 Direct Oxidation of β-Aryl Substituted Aldehydes to α,β-Unsaturated Aldehydes Promoted by an o-Anisidine—Pd(OAc)2 Co-catalyst. — The use of o-anisidine in place of (S)-diphenylprolinol makes the process simpler and more cost-effective. Moreover, the protocol which is effective for aldehydes is complementary to that of the classical Saegusa reaction with ketone-derived silyl enone ethers. — (LIU, J.; ZHU, J.; JIANG, H.; WANG*, W.; LI, J.; Chem. Asian J. 4 (2009) 11, 1712-1716; Sch. Pharm., East China Univ. Chem. Technol., Shanghai 200237, Peop. Rep. China; Eng.) — Bartels 07- 064

ChemInform Abstract: Direct Oxidation of β-Aryl Substituted Aldehydes to α,β-Unsaturated Aldehydes Promoted by an o-Anisidine—Pd(OAc)2 Co-catalyst

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Page 1: ChemInform Abstract: Direct Oxidation of β-Aryl Substituted Aldehydes to α,β-Unsaturated Aldehydes Promoted by an o-Anisidine—Pd(OAc)2 Co-catalyst

www.cheminform.wiley-vch.de

AldehydesQ 0320 DOI: 10.1002/chin.201007064

Direct Oxidation of β-Aryl Substituted Aldehydes to α,β-Unsaturated Aldehydes Promoted by an o-Anisidine—Pd(OAc)2 Co-catalyst. — The use of o-anisidine in place of (S)-diphenylprolinol makes the process simpler and more cost-effective. Moreover, the protocol which is effective for aldehydes is complementary to that of the classical Saegusa reaction with ketone-derived silyl enone ethers. — (LIU, J.; ZHU, J.; JIANG, H.; WANG*, W.; LI, J.; Chem. Asian J. 4 (2009) 11, 1712-1716; Sch. Pharm., East China Univ. Chem. Technol., Shanghai 200237, Peop. Rep. China; Eng.) — Bartels

07- 064

ChemInform 2010, 41, issue 07 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim