cheminform abstract: chiral phosphoric acid catalyzed diastereo- and enantioselective 1,4-conjugate...

ChemInform 2010, 41, issue 39 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Polyphenylalkane derivatives Q 0720 DOI: 10.1002/chin.201039100 Chiral Phosphoric Acid Catalyzed Diastereo- and Enantioselective 1,4-Conjugate Addition of β-Ketoesters to Nitroolefins. — The corresponding adducts (III) are ob- tained in high yields and with moderate diastereoselectivities and enantioselectivities. — (ZHANG, H.; CUN, L.-F.; ZHANG, X.-M.; YUAN*, W.-C.; Lett. Org. Chem. 7 (2010) 3, 219-225 ; Chengdu Inst. Org. Chem., Chin. Acad. Sci., Chengdu 610041, Peop. Rep. China; Eng.) — M. Paetzel 39- 100

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Page 1: ChemInform Abstract: Chiral Phosphoric Acid Catalyzed Diastereo- and Enantioselective 1,4-Conjugate Addition of β-Ketoesters to Nitroolefins

www.cheminform.wiley-vch.de

Polyphenylalkane derivativesQ 0720 DOI: 10.1002/chin.201039100

Chiral Phosphoric Acid Catalyzed Diastereo- and Enantioselective 1,4-Conjugate Addition of β-Ketoesters to Nitroolefins. — The corresponding adducts (III) are ob-tained in high yields and with moderate diastereoselectivities and enantioselectivities. — (ZHANG, H.; CUN, L.-F.; ZHANG, X.-M.; YUAN*, W.-C.; Lett. Org. Chem. 7 (2010) 3, 219-225 ; Chengdu Inst. Org. Chem., Chin. Acad. Sci., Chengdu 610041, Peop. Rep. China; Eng.) — M. Paetzel

39- 100

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