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Volumn 20, Issue 2, 2014, Pages 410-415

βUnsaturated acyl cyanides as new bis-electrophiles for enantioselective organocatalyzed formal [3+3]spiroannulation

Author keywords

Domino reactions; Enantioselectivity; Glutarimides; Organocatalysis; Spiroannulation

Indexed keywords

CYANIDES; REACTION KINETICS;

EID: 84895927976     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201303613     Document Type: Article
Times cited : (51)

References (94)
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    • 38349142750 scopus 로고    scopus 로고
    • Special Issue On Organocatalysis (Ed.: B. List)
    • Special issue on organocatalysis (Ed.: B. List), Chem. Rev. 2007, 107, 5413"
    • (2007) Chem. Rev. , vol.107 , pp. 5413
  • 81
    • 53549109517 scopus 로고    scopus 로고
    • The reactivity of a,b-unsaturated acyl chlorides has been exploited for the efficient generation of acyl azoliums used in enantioselective [4+2]cycloadditions with various dienophiles
    • The reactivity of a,b-unsaturated acyl chlorides has been exploited for the efficient generation of acyl azoliums used in enantioselective [4+2]cycloadditions with various dienophiles: P. S. Tiseni, R. Peters, Angew. Chem. 2007, 119, 5419"
    • (2007) Angew. Chem. , vol.119 , pp. 5419
    • Tiseni, P.S.1    Peters, R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.