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Volumn , Issue 23, 2004, Pages 4894-4900

Dihalogenation of gem-aryl-disubstituted methylenecyclopropanes by DEAD, DIAD/TiX4 or free halogen

Author keywords

Diethyl azodicarboxylate (DEAD); Dihalogenation; Diisopropyl azodicarboxylate (DIAD); Lewis acids; Ring opening reactions

Indexed keywords

2,4 DIHALOBUT 1 ENE; ALKENE DERIVATIVE; BROMINE; CYCLOPROPANE DERIVATIVE; DICARBOXYLIC ACID DERIVATIVE; DIETHYL AZODICARBOXYLIC ACID; DIISOPROPYL AZODICARBOXYLIC ACID; HALOGEN; IODINE; LEWIS ACID; METHYLENECYCLOPROPANE DERIVATIVE; TITANIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 10844254621     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200400388     Document Type: Article
Times cited : (18)

References (51)
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    • note
    • 2 (X = Cl, Br, l) at 65 °C. H.-W.
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    • Hanack and co-workers have reported the dibromination of MCPs 1 with bromine at -5 °C in which 1,2-dibromo-1-methylenecyclopropanes were obtained. [9a] M. Hanack, T. Bassler, W. Eymann, W. E. Heyd, R. Kopp, J. Am. Chem. Soc. 1974, 96, 6686-6691.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.