Molecules 2001, 6(11), 892-899; doi:10.3390/61100892
Article

Captodative Formyl Enamines in a New Synthesis of Tertiary α-Amino Esters

Alexandre Yu. Rulev* email, Lyudmila I. Larina and Mikhail G. Voronkov
A.E.Favorsky Institute of Chemistry, Siberian Division of the Russian Academy of Sciences, 1, Favorsky Str., Irkutsk 664033, Russia
* Author to whom correspondence should be addressed.
Received: 26 February 2001; in revised form: 15 October 2001 / Accepted: 18 October 2001 / Published: 31 October 2001
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Abstract: A strategy to create the –CH(NR2)CO- moiety from captodative formyl enamines was successfully applied to the synthesis of tertiary α-amino esters.
Keywords: Captodative formyl enamine; dialkyl phosphite; α-amino ester

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MDPI and ACS Style

Rulev, A.Y.; Larina, L.I.; Voronkov, M.G. Captodative Formyl Enamines in a New Synthesis of Tertiary α-Amino Esters. Molecules 2001, 6, 892-899.

AMA Style

Rulev AY, Larina LI, Voronkov MG. Captodative Formyl Enamines in a New Synthesis of Tertiary α-Amino Esters. Molecules. 2001; 6(11):892-899.

Chicago/Turabian Style

Rulev, Alexandre Y.; Larina, Lyudmila I.; Voronkov, Mikhail G. 2001. "Captodative Formyl Enamines in a New Synthesis of Tertiary α-Amino Esters." Molecules 6, no. 11: 892-899.

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