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Volumn 22, Issue 2, 2009, Pages 110-117

Quinoline formation via a modified Combes reaction: Examination of kinetics, substituent effects, and mechanistic pathways

Author keywords

Combes quinoline synthesis; Hammett correlation; Kinetics; Steric effects; Substituent effects; Trifluoromethy 1 1,3 diketones

Indexed keywords

ANILINE; KETONES; NITROGEN COMPOUNDS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; POTASSIUM COMPOUNDS;

EID: 60649084680     PISSN: 08943230     EISSN: 10991395     Source Type: Journal    
DOI: 10.1002/poc.1433     Document Type: Article
Times cited : (44)

References (42)
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    • K. M. Muraleedharan, M. A. Avery, Eds, J. B. Taylor, D. J. Triggle, Comprehensive Medicinal Chemistry II, (Vol. 7, p. 765) Elsevier Ltd., Oxford, 2006.
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    • The Friedlander and Pfitzinger methods use an o-carbonyl or o-carboxy aniline, while the Skraup and Doebner-Miller syntheses use an α,β-unsaturated carbonyl electrophile with aniline. See
    • The Friedlander and Pfitzinger methods use an o-carbonyl or o-carboxy aniline, while the Skraup and Doebner-Miller syntheses use an α,β-unsaturated carbonyl electrophile with aniline. See S. A. Yamashkin, E. A. Oreshkina, Chem. Heterocycl. Compos. 2006, 42(6), 2006.
    • (2006) Chem. Heterocycl. Compos , vol.42 , Issue.6 , pp. 2006
    • Yamashkin, S.A.1    Oreshkina, E.A.2
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    • J. Hine, Physical Organic Chemistry, 2nd edn, (pp. 255-257.) McGraw-Hill Book Co., Inc., New York, 1962.
    • J. Hine, Physical Organic Chemistry, 2nd edn, (pp. 255-257.) McGraw-Hill Book Co., Inc., New York, 1962.
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    • 0003956918 scopus 로고
    • McGraw-Hill book Co, Inc, New York
    • L. P. Hammett, Physical Organic Chemistry, (pp. 365-367), McGraw-Hill book Co, Inc., New York, 1970.
    • (1970) Physical Organic Chemistry , pp. 365-367
    • Hammett, L.P.1
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    • m.
    • m.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.