Synthesis of 4-perfluoroalkylquinolines

Tetrahedron

Volumn 54, Issue 28, 1998, Pages 7947-7954

  Strekowski, Lucjan ^a   Lin, Shou Yuan ^a,b   Lee, Hyeran ^a   Zhang, Zhi Qin ^b   Mason, J Christian ^a  

^a GEORGIA STATE UNIVERSITY   (United States)

^b UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4 PERFLUOROALKYLQUINOLINE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; GEL CHROMATOGRAPHY; MOLECULAR DYNAMICS; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 0032500064     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(98)00440-2     Document Type: Article

References (16)

1. [1] For reviews, see: (a) Strekowski L, Lin S-Y, Lee H, Wydra RL, Kiselyov AS. Heterocycl, Commun. 1997; 3: 109.
2. (b) Kiselyov AS, Strekowski L. Org. Prep. Proc. Int. 1996; 28:289.
3. (c) Strekowski L, Kiselyov AS, Trends Heterocycl. Chem. 1993; 3: 73.
4. (d) Kabayashi Y, Kumadaki I. Acc. Chem. Res. 1978; 11:197.
5. [2] Strekowski L, Kiselyov AS, Hojjat M. J. Org. Chem. 1994; 35: 7597.
6. [3] Kiselyov AS, Strekowski L. Tetrahedron Lett. 1994; 35: 7597.
7. [4] Strekowski L, Lin S-Y, Lee H, Mason JC. Tetrahedron Lett. 1996; 37: 4655.
8. [5] Czarny A, Lee H. Say M, Strekowski L. Heterocycles 1997; 45: 2089.
9. [6] Yoshino N, Kitamura M, Seto T, Shibata Y, Abe M, Ogino K. Bull. Chem. Soc. Jpn. 1992; 65: 2141; and references cited therein.
10. [7] Tordeux M, Langlois B, Wakselman C. J. Chem. Soc., Perkin Trans. 1 1990: 2293.
11. [8] Qugmise RJ, Grand DM, Robins RK, Robins RK Jr J. Am. Chem. Soc. 1969; 91: 6381.
12. [9] Patterson SE, Janda L, Strekowski L. J. Heterocycl. Chem. 1992; 29: 703.
13. [10] McCarty GG: The Chemistry of the Carbon-Nitrogen Doable Bond. In: Patai S, editor. London: Interscience, 1970: 376-383.
14. [11] (a) Strekowski L, Patterson SE, Janda L, Wydra RL, Harden DB, Lipowska M, Cegla MT. J. Org. Chem. 1992; 57: 196.
15. (b) Strekowski L, Wydra RL, Cegla MT, Czarny A, Harden DB, Patterson SE, Battiste MA, Coxon JM. J. Org. Chem. 1990; 55:4777.
16. [12] LTMP or LHMDS could be substituted for LDA but the use of NaH or n-BuLi resulted in considerably lower yields of the subsequent cyclization reactions.