메뉴 건너뛰기




Volumn 52, Issue 15, 2013, Pages 4203-4206

Cross-metathesis/iridium(I)-catalyzed allylic etherification strategy: (Iterative) catalytic asymmetric synthesis of syn- and anti-1,2-diols

Author keywords

alcohols; allylation; asymmetric catalysis; iridium; metathesis

Indexed keywords

1 ,2-DIOLS; ASYMMETRIC CATALYSIS; ASYMMETRIC SYNTHESIS; COMPLETE CONTROL; CROSS METATHESIS; DIASTEREO-SELECTIVITY; METATHESIS; REACTION STRATEGIES;

EID: 84875829264     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201209112     Document Type: Article
Times cited : (27)

References (70)
  • 2
    • 0003913629 scopus 로고    scopus 로고
    • in (Ed.: J. Otera), Wiley-VCH, Weinheim
    • G. C. Fu, in Modern Carbonyl Chemistry (Ed.:, J. Otera,), Wiley-VCH, Weinheim, 2000, pp. 69-91.
    • (2000) Modern Carbonyl Chemistry , pp. 69-91
    • Fu, G.C.1
  • 10
    • 70349904185 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 3333-3336.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 3333-3336
  • 13
  • 24
  • 36
    • 36148978554 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 8471-8474
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 8471-8474
  • 40
    • 41949101219 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 1890-1892
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 1890-1892
  • 49
    • 84863229357 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 2717-2721.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 2717-2721
  • 57
    • 79958047257 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 5568-5571
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 5568-5571
  • 59
    • 41949120990 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 1928-1931
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 1928-1931
  • 67
    • 38949095222 scopus 로고    scopus 로고
    • For cross-metathesis of (protected)allylic alcohols, see.
    • For cross-metathesis of (protected)allylic alcohols, see:, I. C. Stewart, C. J. Douglas, R. H. Grubbs, Org. Lett. 2008, 10, 441-444.
    • (2008) Org. Lett. , vol.10 , pp. 441-444
    • Stewart, I.C.1    Douglas, C.J.2    Grubbs, R.H.3
  • 70
    • 67650542570 scopus 로고    scopus 로고
    • Although the free alcohols 5 were prepared by other routes, they can in principle be more efficiently prepared by iridium(I)-catalyzed allylic hydroxylation (Ref.[12d]) followed by CM with B (see the preparation of 5 c in the Supporting Information). The allylic hydroxy group is known to facilitate CM.
    • Although the free alcohols 5 were prepared by other routes, they can in principle be more efficiently prepared by iridium(I)-catalyzed allylic hydroxylation (Ref.[12d]) followed by CM with B (see the preparation of 5 c in the Supporting Information). The allylic hydroxy group is known to facilitate CM:, A. H. Hoveyda, P. J. Lombardi, R. V. O'Brien, A. R. Zhugralin, J. Am. Chem. Soc. 2009, 131, 8378-8379.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 8378-8379
    • Hoveyda, A.H.1    Lombardi, P.J.2    O'Brien, R.V.3    Zhugralin, A.R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.