JOURNAL BROWSE
Search
Advanced SearchSearch Tips
An Efficient Synthesis of 2,3-Dihydro-2-phenyl-4-quinolones from 2'-Aminoacetophenones
facebook(new window)  Pirnt(new window) E-mail(new window) Excel Download
 Title & Authors
An Efficient Synthesis of 2,3-Dihydro-2-phenyl-4-quinolones from 2'-Aminoacetophenones
Lee, Jae-In; Jung, Hye-Jin;
  PDF(new window)
 Keywords
2'-Aminoacetophenones;2'-Aminochalcones;2,3-Dihydro-2-phenyl-4-quinolones;Cyclization;
 Language
English
 Cited by
1.
Molecular Iodine: A Versatile Catalyst for the Synthesis of 2-Aryl-2,3-dihydroquinolin-4(1H)-ones,;;;;

Bulletin of the Korean Chemical Society, 2009. vol.30. 11, pp.2777-2778 crossref(new window)
1.
One-Pot Synthesis of 1,4-Dihydro-2-thioxo-2H-3,1-benzoxazine-4-acetic Acid Derivatives by the Reaction of 2-Isothiocyanatophenyl Ketones with Lithium Enolates of Acetates and Tertiary Acetamides, Helvetica Chimica Acta, 2012, 95, 9, 1561  crossref(new windwow)
2.
Triflic acid promoted fries rearrangement of C-3 vinyl/isopropenyl-azetidin-2-ones: single-pot synthesis of C-3 functionalized-2-aryl-2,3-dihydro-quinoline-4(1H)-ones, RSC Adv., 2014, 4, 79, 41793  crossref(new windwow)
3.
Synthesis of flavanones, azaflavanones, and thioflavanones catalyzed by PMA-SiO2 as a mild, efficient, and reusable catalyst, Monatshefte für Chemie - Chemical Monthly, 2012, 143, 5, 797  crossref(new windwow)
4.
Molecular Iodine: A Versatile Catalyst for the Synthesis of 2-Aryl-2,3-dihydroquinolin-4(1H)-ones, Bulletin of the Korean Chemical Society, 2009, 30, 11, 2777  crossref(new windwow)
5.
Stereoselective Synthesis of Fluorinated 2,3-Dihydroquinolin-4(1H)-ones via a One-Pot Multistep Transformation, The Journal of Organic Chemistry, 2012, 77, 5, 2398  crossref(new windwow)
6.
Antimicrobial ferrocene containing quinolinones: Synthesis, spectral, electrochemical and structural characterization of 2-ferrocenyl-2,3-dihydroquinolin-4(1H)-one and its 6-chloro and 6-bromo derivatives, Polyhedron, 2012, 31, 1, 789  crossref(new windwow)
 References
1.
Singh, O. V.; Kapil, R. S. Synth. Comm. 1993, 23, 277 crossref(new window)

2.
Prakash, O.; Kumar, D.; Saini, R. K; Singh, S. P. Synth. Comm. 1994, 24, 2167 crossref(new window)

3.
Tokes, A. L.; Janzso, G. Synth. Comm. 1989, 19, 3159 crossref(new window)

4.
Donnelly, J. A.; Farrell, D. F. Tetrahedron 1990,46,885 crossref(new window)

5.
Donnelly, J. A.; Farrell, D. F. J. Org. Chem. 1990,55, 1757 crossref(new window)

6.
Tokes, A. L.; Szilagyi, L. Synth. Comm. 1987,17, 1235 crossref(new window)

7.
Tokes, A. L.;Litkei, G; Szilagyi, L. Synth. Comm. 1992, 22, 2433 crossref(new window)

8.
Varma, R. S.; Saini, R. K. Synlett 1997, 857

9.
Kumar, K. H.; Muralidharan, D.; Perumal, P. T. Synthesis 2004, 63

10.
Cho, Y. S.; Kang, K H.; Cha, J. H.; Choi, K. I.; Pae, A. N.; Koh, H. Y.; Chang, M. H. Bull. Korean Chem. Soc. 2002, 23, 1285 crossref(new window)

11.
Park, M. S.; Lee, J. I. Bull. Korean Chem. Soc. 2004, 25, 1269 crossref(new window)

12.
Wattanasin, S.; Murphy, W. S. Synthesis 1980,647