메뉴 건너뛰기




Volumn 51, Issue 38, 2012, Pages 9674-9678

Enantioselective total synthesis of the reported structures of (-)-9-epi-presilphiperfolan-1-ol and (-)-presilphiperfolan-1-ol: Structural confirmation and reassignment and biosynthetic insights

Author keywords

asymmetric catalysis; natural products; structure determination; terpenoids; total synthesis

Indexed keywords

CYCLOADDITION;

EID: 84866357644     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201205276     Document Type: Article
Times cited : (46)

References (74)
  • 12
    • 9844248515 scopus 로고
    • (Eds.: K. L. Dhar, R. K. Thappa, S. G. Agarwal), Tata McGraw-Hill, New Delhi
    • P. Weyerstahl, in Newer Trends in Essential Oils and Flavours (Eds.:, K. L. Dhar, R. K. Thappa, S. G. Agarwal,), Tata McGraw-Hill, New Delhi, 1993, pp. 24-41
    • (1993) Newer Trends in Essential Oils and Flavours , pp. 24-41
    • Weyerstahl, P.1
  • 34
    • 79952498831 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 2756-2760
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 2756-2760
  • 39
    • 36649010386 scopus 로고    scopus 로고
    • Substituted allylic carbamates have been used by Trost to achieve O-acylation of enolates under different reaction conditions. See.
    • Substituted allylic carbamates have been used by Trost to achieve O-acylation of enolates under different reaction conditions. See:, B. M. Trost, J. Xu, J. Org. Chem. 2007, 72, 9372-9375.
    • (2007) J. Org. Chem. , vol.72 , pp. 9372-9375
    • Trost, B.M.1    Xu, J.2
  • 43
    • 27544451620 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 6924-6927
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 6924-6927
  • 54
    • 33747884493 scopus 로고    scopus 로고
    • For a related example of the asymmetric alkylation of vinylogous thioesters, see
    • For a related example of the asymmetric alkylation of vinylogous thioesters, see:, B. M. Trost, R. N. Bream, J. Xu, Angew. Chem. 2006, 118, 3181-3184
    • (2006) Angew. Chem. , vol.118 , pp. 3181-3184
    • Trost, B.M.1    Bream, R.N.2    Xu, J.3
  • 55
    • 33746191949 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 3109-3112.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 3109-3112
  • 59
  • 62
    • 34248648753 scopus 로고    scopus 로고
    • A related IMDA cycloaddition for the construction of an analogous tricyclic system with an activated alkyne has been reported. See.
    • A related IMDA cycloaddition for the construction of an analogous tricyclic system with an activated alkyne has been reported. See:, L. Evanno, A. Deville, B. Bodo, B. Nay, Tetrahedron Lett. 2007, 48, 4331-4333.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 4331-4333
    • Evanno, L.1    Deville, A.2    Bodo, B.3    Nay, B.4
  • 71
    • 0035901668 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 1456-1460.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 1456-1460


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.