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Volumn 44, Issue 48, 2005, Pages 7961-7964

Phenol Ugi-Smiles systems: Strategies for the multicomponent N-arylation of primary amines with isocyanides, aldehydes, and phenols

Author keywords

Amines; Arylation; Multicomponent reaction; Phenols; Rearrangement

Indexed keywords

ALDEHYDES; AMINES; CYANIDES; ESTERS; SYNTHESIS (CHEMICAL);

EID: 29144448797     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200502636     Document Type: Article
Times cited : (180)

References (29)
  • 1
    • 26844537872 scopus 로고    scopus 로고
    • For recent reviews, see: a) L. Banfi, R. Riva, Org. React. 2005, 65, 1-140;
    • (2005) Org. React. , vol.65 , pp. 1-140
    • Banfi, L.1    Riva, R.2
  • 7
    • 0001134412 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 3168-3210.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3168-3210
  • 8
    • 29144532430 scopus 로고    scopus 로고
    • see ret. [3c]
    • These salts are usually added to the reaction mixture in association with amine hydrochlorides; see ret. [3c].
  • 17
    • 0031661388 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1998, 37, 2234-2237;
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 2234-2237
  • 23
    • 0037020334 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 3633-3635.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 3633-3635
  • 24
    • 29144439650 scopus 로고    scopus 로고
    • see ref. [7b,c]
    • If tandem reactions using the heterocyclic core are involved, more components can be included in the process; see ref. [7b,c].
  • 25
    • 33947449188 scopus 로고
    • For examples of Smiles rearrangements, see: a) J. F. Bunnet, R. E. Zahler, Chem. Rev. 1951, 49, 273-308;
    • (1951) Chem. Rev. , vol.49 , pp. 273-308
    • Bunnet, J.F.1    Zahler, R.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.