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Volumn 48, Issue 44, 2007, Pages 7894-7898

Chelation-controlled asymmetric aminohalogenation reaction

Author keywords

4 Phenyl 2 oxazolidinone; Aminohalogenation; Ionic liquids; Palladium(II) acetate

Indexed keywords

3 PHENYL N ACYL N 4 PHENYL 2 OXAZOLIDINONE; ACETONITRILE; CINNAMIC ACID DERIVATIVE; INERT GAS; IONIC LIQUID; N,N DICHLORO 4 TOLUENESULFONAMIDE; OXAZOLIDINONE DERIVATIVE; PALLADIUM ACETATE; TOLUENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 35448944814     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.08.099     Document Type: Article
Times cited : (25)

References (59)
  • 1
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    • Trost B.M., and Fleming I. (Eds), Pergamon, Oxford and references cited therein
    • Kemp J.E.G. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis Vol. 3 (1991), Pergamon, Oxford 471-513 and references cited therein
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 471-513
    • Kemp, J.E.G.1
  • 26
    • 0242491852 scopus 로고    scopus 로고
    • For the recent excellent work on aminohalogenation by several other groups, see:
    • For the recent excellent work on aminohalogenation by several other groups, see:. Qi X., Lee S.H., Kwon J.Y., Kim Y., Kim S.J., Lee Y.S., and Yoon J. J. Org. Chem. 68 (2003) 9140
    • (2003) J. Org. Chem. , vol.68 , pp. 9140
    • Qi, X.1    Lee, S.H.2    Kwon, J.Y.3    Kim, Y.4    Kim, S.J.5    Lee, Y.S.6    Yoon, J.7
  • 48
    • 0004219714 scopus 로고    scopus 로고
    • For a comprehensive review on palladium chemistry, see:. Schlosser M. (Ed), John Wiley & Sons, Ltd. and references cited therein
    • For a comprehensive review on palladium chemistry, see:. Hegedus L.S. In: Schlosser M. (Ed). Organometallics in Synthesis: A Manual. 2nd ed. (2002), John Wiley & Sons, Ltd. 1123-1217 and references cited therein
    • (2002) Organometallics in Synthesis: A Manual. 2nd ed. , pp. 1123-1217
    • Hegedus, L.S.1
  • 55
    • 0037018454 scopus 로고    scopus 로고
    • For an opposite control of asymmetric aldol reaction using similar chiral auxiliary, see:
    • For an opposite control of asymmetric aldol reaction using similar chiral auxiliary, see:. Evans D.A., Downey C.W., Shaw J.T., and Tedrow J.S. Org. Lett. 4 (2002) 1127
    • (2002) Org. Lett. , vol.4 , pp. 1127
    • Evans, D.A.1    Downey, C.W.2    Shaw, J.T.3    Tedrow, J.S.4
  • 59
    • 35448936364 scopus 로고    scopus 로고
    • note
    • 12 followed by the anion metathesis using N-lithiotrifluoromethanesulfonimide in acetone solution (...)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.