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Volumn 135, Issue 44, 2013, Pages 16312-16315

Dihaloiodoarenes: α,α-dihalogenation of phenylacetate derivatives

Author keywords

[No Author keywords available]

Indexed keywords

DIAZOACETATE; DIHALOGENATION; HYPERVALENT IODINE; IODOBENZENE; IODOTOLUENE DIFLUORIDE; LEWIS ACID; LEWIS BASE; PHENYLACETATE;

EID: 84887785496     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja408678p     Document Type: Article
Times cited : (106)

References (55)
  • 30
    • 33947501983 scopus 로고    scopus 로고
    • Diazocarbonyls undergo gem -dihalogenation upon exposure to diatomic halogens or mixed halogen species (e.g., NCS/TBACl, NCS/TBAF, NBS/HF). As iodane 6 formally reacts as diatomic chlorine, it was expected that combining it with a diazoester would result in gem -dichlorination. Zhao, X.-F.; Zhang, C. Synthesis 2007, 551
    • (2007) Synthesis , pp. 551
    • Zhao, X.-F.1    Zhang, C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.