메뉴 건너뛰기




Volumn 48, Issue 8, 2007, Pages 1337-1340

Advantage of in situ generation of N-arylsulfonyl imines from α-amide sulfones in the phase-transfer-catalyzed asymmetric Strecker reaction

Author keywords

Amido sulfones; Amino nitriles; Chiral quaternary ammonium iodide; Potassium cyanide; Strecker synthesis

Indexed keywords

ALKYL GROUP; AMMONIA; IMINE; IODIDE; NITRILE; POTASSIUM CYANIDE; SULFONE DERIVATIVE; TOLUENE;

EID: 33846392229     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.12.122     Document Type: Article
Times cited : (62)

References (43)
  • 34
    • 28444495479 scopus 로고    scopus 로고
    • For recent excellent review on the utility of α-amido sulfones as precursors of N-acylimino derivatives, see:
    • For recent excellent review on the utility of α-amido sulfones as precursors of N-acylimino derivatives, see:. Petrini M. Chem. Rev. 105 (2005) 3949
    • (2005) Chem. Rev. , vol.105 , pp. 3949
    • Petrini, M.1
  • 35
    • 5344262439 scopus 로고    scopus 로고
    • For pioneering study on the synthesis of N-protected α-amino nitriles from α-amide sulfones under phase-transfer conditions, see:
    • For pioneering study on the synthesis of N-protected α-amino nitriles from α-amide sulfones under phase-transfer conditions, see:. Banphavichit V., Chaleawlertumpon S., Bhanthumnavin W., and Vilaivan T. Synth. Commun. 34 (2004) 3147
    • (2004) Synth. Commun. , vol.34 , pp. 3147
    • Banphavichit, V.1    Chaleawlertumpon, S.2    Bhanthumnavin, W.3    Vilaivan, T.4
  • 37
    • 29144448796 scopus 로고    scopus 로고
    • For in situ generation of N-carbamoyl imines from α-amido sulfones in the phase-transfer-catalyzed asymmetric aza-Henry reaction, see:
    • For in situ generation of N-carbamoyl imines from α-amido sulfones in the phase-transfer-catalyzed asymmetric aza-Henry reaction, see:. Fini F., Sgarzani V., Pettersen D., Herrera R.P., Bernardi L., and Ricci A. Angew. Chem., Int. Ed. 44 (2005) 7975
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 7975
    • Fini, F.1    Sgarzani, V.2    Pettersen, D.3    Herrera, R.P.4    Bernardi, L.5    Ricci, A.6
  • 39
    • 0025737610 scopus 로고
    • For this type of abbreviation for multi-substituted benzenesulfonyl groups, see, for example:
    • For this type of abbreviation for multi-substituted benzenesulfonyl groups, see, for example:. Ramage R., Green J., and Blake A.J. Tetrahedron 47 (1991) 6353
    • (1991) Tetrahedron , vol.47 , pp. 6353
    • Ramage, R.1    Green, J.2    Blake, A.J.3
  • 42
    • 33846374476 scopus 로고    scopus 로고
    • note
    • 4,11


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.