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Volumn 64, Issue 10, 2008, Pages 2301-2306

Asymmetric synthesis of trifluoromethylated propargylamines via 1,2-additions of trifluoromethylacetylide to N-tert-butanesulfinyl imines

Author keywords

1,2 Addition; Asymmetric synthesis; Propargylamine; Trifluoromethyl group

Indexed keywords

2 BROMO 3,3,3 TRIFLUOROPROPENE; ACETIC ACID DERIVATIVE; AMINE; IMINE; LITHIUM DERIVATIVE; LITHIUM DIISOPROPYLAMIDE; LITHIUM TRIFLUOROMETHYLACETYLIDE; N TERT BUTANESULFINYLIMINE; PROPARGYLAMINE DERIVATIVE; SULFONAMIDE; TRIFLUOROMETHYLACETYLIDE; UNCLASSIFIED DRUG;

EID: 38649137678     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.01.021     Document Type: Article
Times cited : (22)

References (26)
  • 1
    • 38649129938 scopus 로고    scopus 로고
    • For selected examples, see:
    • For selected examples, see:
  • 13
    • 0002780706 scopus 로고    scopus 로고
    • Asymmetric Fluoroorganic Chemistry:Synthesis, Application, and Future Directions
    • American Chemical Society, Washington, DC
    • Ramachandran P.V. Asymmetric Fluoroorganic Chemistry:Synthesis, Application, and Future Directions. ACS Symposium Series Vol. 746 (2000), American Chemical Society, Washington, DC
    • (2000) ACS Symposium Series , vol.746
    • Ramachandran, P.V.1
  • 23
    • 38649133566 scopus 로고    scopus 로고
    • note
    • Crystal data have been deposited at the Cambridge Crystallographic Data Center with reference number: CCDC 669005.
  • 25
    • 38649122757 scopus 로고    scopus 로고
    • note
    • Crystal data have been deposited at the Cambridge Crystallographic Data Center with reference number: CCDC 667051.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.