Palladium-catalyzed three carbon chain extension reactions with acrolein acetals. A convenient synthesis of conjugated dienals-Reference-Cited by-同舟云学术

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Palladium-catalyzed three carbon chain extension reactions with acrolein acetals. A convenient synthesis of conjugated dienals

Published:1981-03 Issue:6 Volume:46 Page:1061-1067
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Patel Babu A.,Kim Jin-Il I.,Bender Diana D.,Kao Lien-Chung,Heck Richard F.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo00319a004

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2. An Interrupted Vinylogous Iso-Nazarov Reaction: Cycloisomerization of Conjugated Trienones to Cyclopenta[b]furan Derivatives;The Journal of Organic Chemistry;2014-08-13

3. Acrolein Diethyl Acetal: A Three-Carbon Homologating Reagent for the Synthesis of β-Arylpropanoates and Cinnamaldehydes by Heck Reaction Catalyzed by a Kaiser Oxime Resin Derived Palladacycle;European Journal of Organic Chemistry;2008-06

4. The Effects of Ring Size and Substituents on the Rates of Acid-Catalysed Hydrolysis of Five- and Six-Membered Ring Cyclic Ketone Acetals;European Journal of Organic Chemistry;2007-07

5. Preparation of Difunctional Compounds;Compendium of Organic Synthetic Methods;2006-11-22

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