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Volumn 7, Issue 9, 2012, Pages 2014-2018

Highly regioselective synthesis of polysubstituted tetrahydroquinolines by an iodine-induced tandem cyclization reaction from propargylic alcohols and amines

Author keywords

allenes; amines; cyclization; iodine; tetrahydroquinoline

Indexed keywords

ALLENES; AROMATIC AMINES; ENVIRONMENTALLY-FRIENDLY; NATURALLY OCCURRING; PROPARGYL ALCOHOL; PROPARGYLIC ALCOHOLS; REACTION CONDITIONS; REGIOSELECTIVE SYNTHESIS; SYNTHETIC STRATEGIES; TANDEM CYCLIZATION; TETRAHYDROQUINOLINE;

EID: 84865469400     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201200344     Document Type: Article
Times cited : (8)

References (63)
  • 22
  • 48
    • 72449207587 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9875-9878
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9875-9878
  • 57
    • 84865481290 scopus 로고    scopus 로고
    • The molecular structure of the product of the reaction of 2 a was determined by X-ray crystallographic studies. CCDC 875093 (2 a) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.