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Volumn 47, Issue 17, 2006, Pages 2879-2881

Corrigendum to "Preparation of primary arylamines via arylzinc chlorides in good yields". [Tetrahedron Lett. 47 (2006) 2879] (DOI:10.1016/j.tetlet.2006.02.129);Preparation of primary arylamines via arylzinc chlorides in good yields

Author keywords

Arylamines; Electrophilic amination; Organozinc reagents; Oxime

Indexed keywords

1,3 DIMETHYL 3,4,5,6 TETRAHYDRO 2(1H) PYRIMIDINONE; ACETONE O (2,4,6 TRIMETHYLPHENYLSULFONYL)OXIME; AROMATIC AMINE; COPPER; KETONE DERIVATIVE; OXIME DERIVATIVE; UNCLASSIFIED DRUG; ZINC CHLORIDE;

EID: 33645218378     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.04.033     Document Type: Erratum
Times cited : (16)

References (28)
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    • O. Mitsunobu B.M. Trost I. Fleming E. Winterfeldt Comprehensive Organic Synthesis Vol. 6 1991 Pergamon Oxford 65
    • (1991) Comprehensive Organic Synthesis , vol.6 , pp. 65
    • Mitsunobu, O.1
  • 11
    • 0000001279 scopus 로고
    • G. Heimchen R.W. Hoffman J. Mulzer E. Schaumann Thieme Stuttgart
    • G. Boche G. Heimchen R.W. Hoffman J. Mulzer E. Schaumann Houben-Weyl, Methods of Organic Chemistry Vol. E21e 1995 Thieme Stuttgart 5153
    • (1995) Houben-Weyl, Methods of Organic Chemistry , vol.21 , pp. 5153
    • Boche, G.1
  • 28
    • 33645220416 scopus 로고    scopus 로고
    • note
    • 4, the solvent was evaporated and the crude product was converted to its N-benzoyl derivative by reaction with benzoyl chloride in the presence of NaOH. The product was recrystallized from ethanol-water (4:1).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.