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Volumn 47, Issue 47, 2006, Pages 8235-8238

Corrigendum to "Asymmetric allylation of N-benzoylhydrazones promoted by novel C2-symmetric bis-sulfoxide organocatalysts". [Tetrahedron Lett. 47 (2006) 8235] (DOI:10.1016/j.tetlet.2006.09.113);Asymmetric allylation of N-benzoylhydrazones promoted by novel C2-symmetric bis-sulfoxide organocatalysts

Author keywords

Chiral sulfoxide; Chiral sulfur reagents; Enantioselective allylation; Organocatalysis

Indexed keywords

ALDEHYDE; HYDRAZONE DERIVATIVE; KETONE; LITHIUM DERIVATIVE; OXIDE; PYRIDINE DERIVATIVE; SULFOXIDE;

EID: 33750017562     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.02.122     Document Type: Erratum
Times cited : (42)

References (55)
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    • Yamamoto H. Lewis Acids in Organic Synthesis Vols. 1 and 2 (1999), Wiley-VCH, Weinheim and references cited therein
    • (1999) Lewis Acids in Organic Synthesis , vol.1-2
    • Yamamoto, H.1
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    • 33846104288 scopus 로고    scopus 로고
    • Malkov, A. V.; Kocovsky, P. Eur. J. Org. Chem., doi:10.1002/ejoc.200600474.
  • 27
    • 33750022012 scopus 로고    scopus 로고
    • See also Ref. 6b.
  • 37
    • 0000474038 scopus 로고
    • Allinger N.L., Eliel E.L., and Wilen S. (Eds), Wiley, New York
    • Mikolajczyk M., and Drabowicz J. In: Allinger N.L., Eliel E.L., and Wilen S. (Eds). Topics in Stereochemistry Vol. 13 (1982), Wiley, New York 333-468
    • (1982) Topics in Stereochemistry , vol.13 , pp. 333-468
    • Mikolajczyk, M.1    Drabowicz, J.2
  • 38
    • 0000634441 scopus 로고
    • Morrison J.D. (Ed), Academic Press, New York Chapter 8
    • Posner G.H. In: Morrison J.D. (Ed). Asymmetric Synthesis Vol. 2 (1983), Academic Press, New York 225-241 Chapter 8
    • (1983) Asymmetric Synthesis , vol.2 , pp. 225-241
    • Posner, G.H.1
  • 51
    • 33749999199 scopus 로고    scopus 로고
    • note
    • 2: C, 63.13; H, 5.30; N, 3.51; S, 16.05. Found: C, 63.07; H, 5.36; N, 3.55; S, 16.19.
  • 53
    • 33749995456 scopus 로고    scopus 로고
    • note
    • 2: C, 65.77; H, 5.52; N, 3.65. Found: C, 65.89; H, 5.76; N, 3.68.
  • 54
    • 33750021113 scopus 로고    scopus 로고
    • note
    • 2-EtOAc (2:1) in 72-87% yields.
  • 55
    • 33750031257 scopus 로고    scopus 로고
    • note
    • HPLC: Chiralcel OD, 0.46 cm × 25 cm, hexane-2-propanol (90:10), flow 1.0 mL/min, UV detector at 230 nm. Elution times: (R)-8a, 8.8 min; (S)-8a, 9.8 min. (R)-8b, 12.7 min; (S)-8b, 14.6 min. (R)-8c, 16.5 min; (S)-8c, 21.2 min. (R)-8d, 11.1 min; (S)-8d, 16.2 min. (R)-8e, 12.0 min; (S)-8e, 10.0 min. (S)-8f, 10.8 min; (R)-8f, 13.6 min.


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