ChemInform Abstract: Carbon-Carbon Double Bond Formation Between α-Halo Ketones and Aldehydes Mediated by SnCl2/Na2SO3: Synthesis of E-α,β- Unsaturated Ketones.

ChemInform ◽  
2010 ◽  
Vol 24 (32) ◽  
pp. no-no
Author(s):  
R. LIN ◽  
Y. YU ◽  
Y. ZHANG
Keyword(s):  
Double Bond ◽  
Bond Formation ◽  
Unsaturated Ketones ◽  
Carbon Double Bond

scholarly journals Chemoselective and metal-free reduction of α,β-unsaturated ketones by in situ produced benzeneselenol from O-(tert-butyl) Se-phenyl selenocarbonate

RSC Advances ◽  
2020 ◽  
Vol 10 (56) ◽  
pp. 33706-33717
Author(s):  
Andrea Temperini ◽  
Marco Ballarotto ◽  
Carlo Siciliano
Keyword(s):  
Double Bond ◽  
Hydrochloric Acid ◽  
Unsaturated Ketones ◽  
Metal Free ◽  
Tert Butyl ◽  
Carbon Double Bond

The carbon–carbon double bond of arylidene acetones and chalcones can be selectively reduced with benzeneselenol generated in situ by reacting O-(tert-butyl) Se-phenyl selenocarbonate with hydrochloric acid in ethanol.

Neodymium-Promoted Highly Selective Carbon–Carbon Double Bond Formation of Ketones with Allyl Halides in the Presence of Diethyl Phosphite

Synthesis ◽  
2020 ◽  
Vol 52 (22) ◽  
pp. 3446-3451
Author(s):  
Songlin Zhang ◽  
Dengbing Xie ◽  
Yiqiong Wang ◽  
Bo Yang
Keyword(s):  
Double Bond ◽  
Bond Formation ◽  
Point Of View ◽  
Diethyl Phosphite ◽  
Reaction Conditions ◽  
One Pot ◽  
Mild Conditions ◽  
Carbon Double Bond ◽  
Allyl Halides ◽  
First Time

The carbon–carbon double bond formation via neodymium-mediated Barbier-type reaction of ketones and allyl halides in the presence of diethyl phosphite is reported for the first time. The reaction is highly α-regioselective and was conveniently carried out under mild conditions in a one-pot fashion. From a synthetic point of view, a series of conjugated alkenes were obtained in moderate to good yields in this one-pot reaction with feasible reaction conditions.

Silyl-substituted α,β-Unsaturated Ketones from the Reaction of Silylvinylmetallic Reagents with Acid Anhydrides

1973 ◽  
Vol 51 (12) ◽  
pp. 2024-2032 ◽  
Author(s):  
A. G. Brook ◽  
J. M. Duff
Keyword(s):  
Double Bond ◽  
Low Temperatures ◽  
Silyl Group ◽  
Unsaturated Ketones ◽  
Carbon Double Bond ◽  
Benzoic Anhydride ◽  
Acid Anhydrides ◽  
By Products

The reactions of a series of silyl-substituted vinylmetallic reagents with acetic and benzoic anhydride have been investigated as a general route to α,β-unsaturated ketones having a silyl group attached to the carbon–carbon double bond. The reaction has been found to be generally applicable for acetyl derivatives provided low temperatures are used but the reaction with benzoic anhydride gives poorer results. The i.r. and u.v. spectra of the ketones are discussed. The characterization of novel 1,4-dienes obtained as by-products in the syntheses is also described.

ChemInform Abstract: Carbon-Carbon Double Bond Formation from a cis-Bis(chloromethyl) Complex.

ChemInform ◽  
2010 ◽  
Vol 23 (11) ◽  
pp. no-no
Author(s):  
J. L. HUBBARD ◽  
A. MORNEAU ◽  
R. M. BURNS ◽  
O. W. NADEAU
Keyword(s):  
Double Bond ◽  
Bond Formation ◽  
Carbon Double Bond
Sign in / Sign up

Export Citation Format

Share Document