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Volumn , Issue 6, 2005, Pages 1113-1128

An asymmetric biaryl Suzuki cross-coupling reaction: Stereogenic benzylic carbinols as chiral auxiliaries

Author keywords

Asymmetric synthesis; Cross coupling; Palladium; Stereogenic carbinol; Sulfoxides; Suzuki reaction

Indexed keywords

BENZENE DERIVATIVE; BENZYL ALCOHOL; BORONIC ACID DERIVATIVE; HALIDE; KORUPENSAMINE A; METHANOL DERIVATIVE; PALLADIUM COMPLEX; STEGANACIN; SULFOXIDE; UNCLASSIFIED DRUG; VANCOMYCIN;

EID: 15944407157     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200400638     Document Type: Article
Times cited : (33)

References (55)
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    • (Eds.: B. M. Trost, I. Fleming), Pergamon Press, New York
    • a) D. W. Knight, in Comprehensive Organic Synthesis (Eds.: B. M. Trost, I. Fleming), Pergamon Press, New York, 1991, vol. 3, p. 481;
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 481
    • Knight, D.W.1
  • 6
    • 0000718373 scopus 로고    scopus 로고
    • L. Pu, Chem. Rev. 1998, 98, 2405-2494.
    • (1998) Chem. Rev. , vol.98 , pp. 2405-2494
    • Pu, L.1
  • 41
    • 15944419919 scopus 로고    scopus 로고
    • note
    • 3].
  • 44
    • 15944428268 scopus 로고    scopus 로고
    • note
    • 1H NMR studies: the chemical shifts of the two methylene protons α to the sulfoxide group were significantly different.
  • 46
    • 15944409260 scopus 로고    scopus 로고
    • note
    • 1H NMR studies: the chemical shifts of the methoxy and the methyl(p-tolyl) groups were significantly different.
  • 52
    • 15944397335 scopus 로고    scopus 로고
    • note
    • We oxidized 17 using the same experimental procedure as for the synthesis of 41 starting from 12 (see Experimental Section).
  • 53
    • 15944405405 scopus 로고    scopus 로고
    • note
    • Reduction of 17 and 45 was performed in MeOH using Raney Ni at room temperature.
  • 54
    • 15944383831 scopus 로고    scopus 로고
    • note
    • We thank Dr. Nathalie Gruber for assistance with the analysis of the crystal structure (Service commun Rayons X, 4 rue Blaise Pascal, 67070 Strasbourg cedex, E-mail: sercomrx@chimie.u-strasbg.fr).
  • 55
    • 15944399112 scopus 로고    scopus 로고
    • Interactive Structure Solution, Nonius B. V., Delft, The Netherlands
    • OpenMolEn, Interactive Structure Solution, Nonius B. V., Delft, The Netherlands, 1997.
    • OpenMolEn , pp. 2004


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.