Friedel—Crafts Reaction with Silicon-Containing Acid Chlorides as a Synthetic Route to Compounds and Polymers

1965 ◽  
Vol 30 (9) ◽  
pp. 2889-2896 ◽  
Author(s):  
E. V. Wilkus ◽  
W. H. Rauscher
Keyword(s):  
Acid Chlorides ◽  
Synthetic Route

A synthetic route to highly substituted ketones. Acylations of .alpha. anions of carboxylic acid salts with acid chlorides

1977 ◽  
Vol 42 (7) ◽  
pp. 1189-1194 ◽  
Author(s):  
A. Paul Krapcho ◽  
David S. Kashdan ◽  
E. G. E. Jahngen ◽  
A. J. Lovey
Keyword(s):  
Carboxylic Acid ◽  
Acid Chlorides ◽  
Synthetic Route ◽  
Acid Salts

Cleavage of silicon-nitrogen bonds by acid chlorides: an unusual synthetic route to amides

1983 ◽  
Vol 48 (22) ◽  
pp. 4111-4113 ◽  
Author(s):  
James R. Bowser ◽  
Pamela J. Williams ◽  
Kenneth Kurz
Keyword(s):  
Acid Chlorides ◽  
Synthetic Route ◽  
Nitrogen Bonds

A General Convergent Strategy for the Synthesis of Tetrasubstituted Furan Fatty Acids (FuFAs)

2019 ◽  
Author(s):  
Yamin Wang ◽  
Gareth Pritchard ◽  
Marc Kimber
Keyword(s):  
Fatty Acids ◽  
Spectral Data ◽  
Synthetic Route ◽  
Furan Fatty Acids

Synthetic route for the synthesis of tetrasubstituted furan fatty acids; including experimental details, characterisation, and spectral data of all intermediates.

Palladium-Catalyzed Asymmetric Annulation Between Aryl Iodides and Racemic Epoxides Using a Chiral Norbornene Cocatalyst

2018 ◽  
Author(s):  
Guangbin Dong ◽  
Renhe Li
Keyword(s):  
Isopropyl Ester ◽  
Synthetic Route ◽  
Initial Development ◽  
Aryl Iodides ◽  
Palladium Catalyzed

Herein, we describe our initial development of an asymmetric Pd-catalyzed annulation between aryl iodides and racemic epoxides for synthesis of 2,3-dihydrobenzofurans using a chiral norbornene cocatalyst. A series of enantiopure ester-, amide- and imide-substituted norbornenes have been prepared with a reliable synthetic route. Promising enantioselectivity (42-45% ee) has been observed using the isopropyl ester-substituted norbornene (N1*) and the amide-substituted norbornene (N7*).

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