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Volumn 50, Issue 48, 2011, Pages 11465-11469

Rhodium-catalyzed reaction of 1-alkenylboronates with aldehydes leading to allylation products

Author keywords

aldehydes; allylation; diastereoselectivity; isomerization; rhodium

Indexed keywords

ALLYLATION PRODUCTS; DIASTEREO-SELECTIVITY; DIASTEREOSELECTIVE; HOMOALLYLIC ALCOHOL; RHODIUM-CATALYZED; SYNTHETIC EQUIVALENTS;

EID: 81755183034     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201105148     Document Type: Article
Times cited : (39)

References (34)
  • 1
    • 0002446724 scopus 로고
    • (Eds.: B.M. Trost, I. Fleming, C.H. Heathcock), Pergamon, Oxford, UK
    • W. R. Roush, Comprehensive Organic Synthesis, Vol.2 (Eds.:, B.M. Trost, I. Fleming, C.H. Heathcock,), Pergamon, Oxford, UK, 1991, pp. 1-53
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 1-53
    • Roush, W.R.1
  • 6
    • 34447526812 scopus 로고    scopus 로고
    • (Ed.: S.E. Denmark), Wiley, New York, and references therein
    • H. Lachance, D. G. Hall, Organic Reactions, Vol.73 (Ed.:, S.E. Denmark,), Wiley, New York, 2008, and references therein.
    • (2008) Organic Reactions, Vol.73
    • Lachance, H.1    Hall, D.G.2
  • 7
    • 34447529397 scopus 로고    scopus 로고
    • (Ed.: D.G. Hall), Wiley-VCH, Weinheim, chap. 6
    • J. W. J. Kennedy, D. G. Hall, Boronic Acids (Ed.:, D.G. Hall,), Wiley-VCH, Weinheim, 2005, chap. 6, pp. 241-277.
    • (2005) Boronic Acids , pp. 241-277
    • Kennedy, J.W.J.1    Hall, D.G.2
  • 22
    • 84906450372 scopus 로고    scopus 로고
    • (Eds.: R.H. Crabtree, D.M.P. Mingos, I. Ojima), Elsevier, Oxford, UK
    • For a recent review on transition-metal-catalyzed alkene isomerization, see:, K. Tanaka, Comprehensive Organometallic Chemistry III, Vol.10 (Eds.:, R.H. Crabtree, D.M.P. Mingos, I. Ojima,), Elsevier, Oxford, UK, 2007, p. 71.
    • (2007) Comprehensive Organometallic Chemistry III , vol.10 , pp. 71
    • Tanaka, K.1
  • 28
    • 0000995725 scopus 로고
    • The reaction using chiral 1-alkenylboronic ester derived from tartaric acid diisopropyl ester (see:, W. R. Roush, A. E. Walts, L. K. Hoong, J. Am. Chem. Soc. 1985, 107, 8186) gave low enantioselectivity, probably owing to the high reaction temperature.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 8186
    • Roush, W.R.1    Walts, A.E.2    Hoong, L.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.