Diastereoselective Enolate Coupling through Redox Umpolung in Silicon and Titanium Bisenolates: A Novel Concept Based on Intramolecularization of Carbon−Carbon Bond Formation-Reference-Cited by-同舟云学术

Diastereoselective Enolate Coupling through Redox Umpolung in Silicon and Titanium Bisenolates: A Novel Concept Based on Intramolecularization of Carbon−Carbon Bond Formation

Published:1998-01-01 Issue:2 Volume:63 Page:396-400
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Schmittel Michael¹,Burghart Armin¹,Malisch Wolfgang¹,Reising Joachim¹,Söllner Rolf¹

Affiliation:

1. Institut für Organische Chemie and Institut für Anorganische Chemie der Universität Würzburg, Am Hubland, D-97074 Würzburg, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo971650x

Reference27 articles.

1. Oxidative Addition of Dimethyl Sodiomalonate and Sodioacetylacetone to Olefins

2. Reaction of ester enolates with copper(II) salts. Synthesis of substituted succinate esters

3. Electrochemical oxidation of the enolate of dibenzoylmethane

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