Chiral Homoenolate Equivalents, V. Hydroxylakylation of Lithiated 3‐[( S )‐2‐(Methoxymethyl)pyrrolidino]‐1,3‐diphenylpropene – An Asymmetric Homoaldol Reaction
Author:
Affiliation:
1. Institut für Organische Chemie der Universität Gießen, Heinrich‐Buff‐Ring 58, D‐35392 Gießen, Germany Telefax: (internat.) +49(0)641‐702‐5712
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19961291004
Reference63 articles.
1. – [1b]A.Kramer Dissertation University of Gießen 1995.
2. [2a]G.Zimmermann Dissertation University of Gießen 1985
3. Chirale Homoenolat‐Äquivalente, II: Asymmetrische Synthese 3‐substituierter Phenylpropionaldehyde über metallierte chirale Cinnamylamine
4. – [2c]L.Santowski Dissertation University of Gießen 1992.
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5. ChemInform Abstract: Chiral Homoenolate Equivalents. Part 5. Hydroxyalkylation of Lithiated 3-((S)-2-(Methoxymethyl)pyrrolidino)-1,3-diphenylpropene - An Asymmetric Homoaldol Reaction.;ChemInform;2010-08-04
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