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Volumn 60, Issue 45, 2004, Pages 10165-10169

Extension of β-chloroenals to ethyl 5-chloro-2,4-pentadienoates using Wadsworth-Emmons reactions: Subsequent conversions to 5-aryl-5-chloro-2,4- pentadienoic acids and 5-aryl-2-penten-4-ynoic acids

Author keywords

Chlorodienoates; Chloroenals; Enynoic acids

Indexed keywords

5 (4 CHLOROPHENYL)PENT 2 EN 4 YNOIC ACID; 5 (4 FLUOROPHENYL)PENT 2 EN 4 YNOIC ACID; 5 (4 METHOXYPHENYL) 2 PENTEN 4 YNOIC ACID; 5 (4 METHYLPHENYL) 2 PENTEN 4 YNOIC ACID; 5 CHLORO 5 (4 CHLOROPHENYL) 2,4 PENTADIENOIC ACID; 5 CHLORO 5 (4 FLUOROPHENYL) 2,4 PENTADIENOIC ACID; 5 CHLORO 5 (4 METHOXYPHENYL) 2,4 PENTADIENOIC ACID; 5 CHLORO 5 (4 METHYLPHENYL) 2,4 PENTADIENOIC ACID; 5 CHLORO 5 PHENYL 2,4 PENTADIENOIC ACID; 5 PHENYLPENT 2 EN 4 YNOIC ACID; ACID; CHLORINE DERIVATIVE; ETHYL 5 CHLORO 5 (3',4' METHYLENEDIOXYPHENYL) 2,4 PENTADIENOATE; ETHYL 5 CHLORO 5 (4 CHLOROPHENYL) 2,4 PENTADIENOATE; ETHYL 5 CHLORO 5 (4 FLUOROPHENYL) 2,4 PENTADIENOATE; ETHYL 5 CHLORO 5 (4 METHOXYPHENYL) 2,4 PENTADIENOATE; ETHYL 5 CHLORO 5 (4 METHYLPHENYL) 2,4 PENTADIENOATE; ETHYL 5 CHLORO 5 PHENYL 2,4 PENTADIENOATE; UNCLASSIFIED DRUG;

EID: 4644301106     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.09.028     Document Type: Article
Times cited : (5)

References (26)
  • 24
    • 84989482624 scopus 로고
    • The 3-chloropropenals were easily prepared from commercially available acetophenones using standard methods: J. Liebscher, and H. Hartmann Synthesis 1979 241
    • (1979) Synthesis , pp. 241
    • Liebscher, J.1    Hartmann, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.