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Volumn 12, Issue 25, 2006, Pages 6684-6691

Iterative deoxypropionate synthesis based on a copper-mediated directed allylic substitution: Formal total synthesis of borrelidin (C3-C11 fragment)

Author keywords

Allylation; Asymmetric synthesis; Diastereoselectivity; Grignard reagents; Polyketides

Indexed keywords

ALLYLATION; ASYMMETRIC SYNTHESIS; DIASTEREOSELECTIVITY; GRIGNARD REAGENTS; POLYKETIDES;

EID: 33748559150     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200600343     Document Type: Article
Times cited : (46)

References (47)
  • 9
    • 4344641299 scopus 로고    scopus 로고
    • for a substrate controlled diastereoselective conjugate addition furnishing syn-deoxypropionate structures see; S. Hanessian, V. Mascitti, S. Giroux, Proc. Natl. Acad. Sci. USA 2004, 101, 11996-12001.
    • (2004) Proc. Natl. Acad. Sci. USA , vol.101 , pp. 11996-12001
    • Hanessian, S.1    Mascitti, V.2    Giroux, S.3
  • 16
    • 4544273059 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 3786-3789;
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 3786-3789
  • 18
    • 4544352550 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 3790-3792; for an alternative approach employing allylic substitution see;
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 3790-3792
  • 20
    • 33748532673 scopus 로고    scopus 로고
    • a) Novozym 435 is a lipase from Candida antarctica lipase B, hydrolase. For more details see www.novozymes.com;
  • 40
    • 4544250290 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 3947-3951;
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 3947-3951
  • 42
    • 33748544463 scopus 로고    scopus 로고
    • note
    • -1.
  • 47
    • 33748528454 scopus 로고    scopus 로고
    • note
    • Magnesium was activated with an ethereal solution of dibromoethane and washed with diethyl ether.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.