Notes: Condensation of Aromatic Aldehydes with Methyl Aryl Ketones and Sodium Cyanide

1959 ◽  
Vol 24 (6) ◽  
pp. 880-882 ◽  
Author(s):  
R Davis
Keyword(s):  
Aromatic Aldehydes ◽  
Sodium Cyanide ◽  
Aryl Ketones

The NHCs-mediated cross-coupling of aromatic aldehydes with benzyl halides: synthesis of α-aryl ketones

2010 ◽  
Vol 51 (27) ◽  
pp. 3571-3574 ◽  
Author(s):  
Lu Lin ◽  
Yi Li ◽  
Wenting Du ◽  
Wei-Ping Deng
Keyword(s):  
Cross Coupling ◽  
Aromatic Aldehydes ◽  
Aryl Ketones ◽  
Benzyl Halides

Comparison of different reducing systems in the synthesis of functionally substituted benzylamines from alkyl aryl ketones and aromatic aldehydes

2010 ◽  
Vol 46 (7) ◽  
pp. 1021-1028 ◽  
Author(s):  
D. M. Musatov ◽  
E. V. Starodubtseva ◽  
O. V. Turova ◽  
D. V. Kurilov ◽  
M. G. Vinogradov ◽  
...  
Keyword(s):  
Aromatic Aldehydes ◽  
Alkyl Aryl ◽  
Aryl Ketones

Base-promoted domino reaction for the synthesis of 2,3-disubstituted indoles from 2-aminobenzaldehyde/2-amino aryl ketones, tosylhydrazine, and aromatic aldehydes

Tetrahedron ◽  
2016 ◽  
Vol 72 (32) ◽  
pp. 4821-4826 ◽  
Author(s):  
Yan-Dong Wu ◽  
Jun-Rui Ma ◽  
Wen-Ming Shu ◽  
Kai-Lu Zheng ◽  
An-Xin Wu
Keyword(s):  
Aromatic Aldehydes ◽  
Domino Reaction ◽  
Aryl Ketones

Nickel N-heterocyclic carbene-catalyzed cross-coupling reaction of aryl aldehydes with organozinc reagents to produce aryl ketones

2015 ◽  
Vol 5 (9) ◽  
pp. 4341-4345 ◽  
Author(s):  
Cheng Jin ◽  
Lijun Gu ◽  
Minglong Yuan
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
Aromatic Aldehydes ◽  
Aryl Aldehydes ◽  
Cross Coupling Reaction ◽  
Aryl Ketones ◽  
Organozinc Reagents ◽  
Synthetic Utilization

The transformation of aromatic aldehydes into aryl ketones by nickel-catalyzed cross-coupling has been developed. This transformation represents an efficient and attractive synthetic utilization of organozinc reagents.

ChemInform Abstract: Comparison of Different Reducing Systems in the Synthesis of Functionally Substituted Benzylamines from Alkyl Aryl Ketones and Aromatic Aldehydes.

ChemInform ◽  
2010 ◽  
Vol 42 (3) ◽  
pp. no-no
Author(s):  
D. M. Musatov ◽  
E. V. Starodubtseva ◽  
O. V. Turova ◽  
D. V. Kurilov ◽  
M. G. Vinogradov ◽  
...  
Keyword(s):  
Aromatic Aldehydes ◽  
Alkyl Aryl ◽  
Aryl Ketones

Tandem nucleophilic addition–Oppenauer oxidation of aromatic aldehydes to aryl ketones with triorganoaluminium reagents

2013 ◽  
Vol 11 (27) ◽  
pp. 4429 ◽  
Author(s):  
Ying Fu ◽  
Yanshou Yang ◽  
Helmut M. Hügel ◽  
Zhengyin Du ◽  
Kehu Wang ◽  
...  
Keyword(s):  
Nucleophilic Addition ◽  
Aromatic Aldehydes ◽  
Aryl Ketones ◽  
Oppenauer Oxidation

scholarly journals Chalcones: A Solubility Study at Different Temperatures

2014 ◽  
Vol 31 ◽  
pp. 7-19
Author(s):  
Ankita A. Bhalu ◽  
Kapil D. Bhesaniya ◽  
Nayan J. Vekariya ◽  
Shipra H. Baluja
Keyword(s):  
Gravimetric Method ◽  
Aromatic Aldehydes ◽  
Solubility Study ◽  
Apelblat Equation ◽  
Modified Apelblat Equation ◽  
Aryl Ketones ◽  
Different Temperatures ◽  
Experimental Solubility Data ◽  
Hoff Equation ◽  
Structure In Solution

Some new chalcones are synthesized by the condensation of aryl ketones with aromatic aldehydes and solubility of these synthesized chalcones is determined in chloroform and dichloromethane at temperatures ranging between 293.15 K and 313.15 K by gravimetric method. The experimental data was correlated well with modified Apelblat equation. Further, from the experimental solubility data, some thermodynamic parameters such as dissolution enthalpy, Gibb’s energy and entropy etc. were evaluated using van’t Hoff equation. The positive Gibb’s energy and negative entropy suggests spontaneous dissolution and more ordered structure in solution.

ChemInform Abstract: Tandem Nucleophilic Addition-Oppenauer Oxidation of Aromatic Aldehydes to Aryl Ketones with Triorganoaluminum Reagents.

ChemInform ◽  
2013 ◽  
Vol 44 (42) ◽  
pp. no-no
Author(s):  
Ying Fu ◽  
Yanshou Yang ◽  
Helmut M. Huegel ◽  
Zhengyin Du ◽  
Kehu Wang ◽  
...  
Keyword(s):  
Nucleophilic Addition ◽  
Aromatic Aldehydes ◽  
Aryl Ketones ◽  
Oppenauer Oxidation
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