Evidence for a Non-Concerted, Dissoziative Mechanism of the Palladium-Catalyzed “Enolate Claisen Rearrangement” of Allylic Esters-Reference-Cited by-同舟云学术

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Evidence for a Non-Concerted, Dissoziative Mechanism of the Palladium-Catalyzed “Enolate Claisen Rearrangement” of Allylic Esters

Published:2010-08-24 Issue:28 Volume:2010 Page:5369-5372
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Braun Manfred,Meletis Panos,Schrader Wolfgang

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference48 articles.

1. The Claisen Rearrangement. Methods and Applications M. Hiersemann U. Nubbemeyer) Wiley-VCH Weinheim 2007

2. Claisen Rearrangement over the Past Nine Decades

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1. A convenient synthesis of fluorinated vinyl ethers derived from di-O-isopropylidenehexofuranose and O-isopropylidenepentofuranose;Journal of Fluorine Chemistry;2014-11

2. “Dba-free” palladium intermediates of the Heck–Matsuda reaction;Organic & Biomolecular Chemistry;2013

3. Palladium-Catalyzed Allylic Alkylation of Carboxylic Acid Derivatives: N-Acyloxazolinones as Ester Enolate Equivalents;Angewandte Chemie International Edition;2011-11-16

4. Palladium-Catalyzed Allylic Alkylation of Carboxylic Acid Derivatives: N-Acyloxazolinones as Ester Enolate Equivalents;Angewandte Chemie;2011-11-16

5. Rearrangement of Aryl- and Benzylthiopyridinium Imides with Participation of a Methyl Substituent;The Journal of Organic Chemistry;2011-10-27

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