cas 4264-35-1, 2-ACETYLINDOLE | Articles data ｜lookchem

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4264-35-1

Articles about 4264-35-1Total 6 be found

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Imidazolium Triflate Ionic Liquid Improves the Activity of ZnCl2 in the Synthesis of Pyrroles and Ketones
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Nguyen, Hai Truong,Ngo, Dung Kim Thi,Chau, Khiem Duy Nguyen,Tran, Phuong Hoang
p. 157 - 165
(2021/03/16)

Photochemistry of ortho -Azidocinnamoyl Derivatives: Facile and Modular Synthesis of 2-Acylated Indoles and 2-Substituted Quinolines under Solvent Control
The light-promoted potential of ortho -azidocinnamoyl compounds is evaluated for heterocycle synthesis. Depending on the nature of the solvent, 2-acylated indoles were obtained under aprotic conditions, whereas the use of a protic medium led to 2-substituted quinolines. The synthetic significance of this metal-free method is that, by simply changing the solvent, the reaction outcome can be directed towards different key heterocyclic scaffolds.
Chaabouni,Pinkerton,Abid,Galaup,Chassaing
p. 2614 - 2618
(2017/10/06)

Iodine-mediated intramolecular amination of ketones: The synthesis of 2-acylindoles and 2-acylindolines by tuning N-protecting groups
A general method for constructing both 2-acylindoles and 2-acylindolines via I2-mediated intramolecular C-N bond formation is presented, and the selective formation of either 2-acylindoles or 2-acylindolines just depends on the nitrogen protecting groups used in the same substrate skeletons. The Royal Society of Chemistry.
Gao, Wen-Chao,Jiang, Shan,Wang, Ruo-Lin,Zhang, Chi
supporting information
p. 4890 - 4892
(2013/07/05)

Novel indole-ring construction method for the synthesis of 2-trifluoromethylindoles
Novel indole-ring construction method, which is particularly effective for the synthesis of 2-perfluoroalkylindoles, and introduction of a cyanomethyl group at C-3 of 2-perfluoroalkylindoles by means of the Mannich reaction are described.
Miyashita, Kazuyuki,Tsuchiya, Katsutoshi,Kondoh, Katsunori,Miyabe, Hideto,Imanishi, Takeshi
p. 513 - 516
(2007/10/03)

THE FORMATION OF SUBSTITUTED INDOLES BY ACID CATALYZED REARRANGEMENTS OF 4-ISOXAZOLINES
Thermal rearrangements of 4-isoxazolines from C,N-diphenylnitrone and substituted alkynes have been directed towards the formation of substituted indoles.Detection and isolation of the intermediates of the process elucidate the reaction pathway.The appropriate choice of substituents and experimental conditions has allowed the control of the single steps involved in the total process.
Liguori, Angelo,Ottana', Rosaria,Romeo, Giovanni,Sindona, Giovanni,Uccella, Nicola
p. 1365 - 1376
(2007/10/02)

New Syntheses of 2-Acylbenzofurans, 2-Acylindoles, 2-Indolylcarboxylates, and 2-Quinolones by Intramolecular Wittig Reaction
The title compounds are obtained by intramolecular Wittiig reaction of 2-(α-ketoacyloxy)-, 2-(α-ketoacylamino)-, or 2-benzyltriphenylphosphonium salts, respectively.
Capuano, Lilly,Ahlhelm, Alfred,Hartmann, Herbert
p. 2069 - 2074
(2007/10/02)

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Chemical Properties

Melting Point: 154-155 °C
Boiling Point: 333.9 °C at 760 mmHg
Flash Point:163.7 °C
Density: 1.193 g/cm³
Storage Temp.:Refrigerator
Vapor Pressure: 0.000132mmHg at 25°C
Refractive Index: 1.648
PKA: 14.79±0.30(Predicted)
PSA: 32.86000
LogP: 2.37050

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