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Volumn 18, Issue 38, 2012, Pages 11880-11883

Asymmetric allylic alkylation of acyclic allylic ethers with organolithium reagents

Author keywords

allylic alkylation; allylic ethers; copper; Lewis acids; organolithium reagents

Indexed keywords

ALLYL ETHERS; ALLYLIC ALKYLATION; ALLYLIC ETHERS; ASYMMETRIC ALLYLIC ALKYLATIONS; C-C BOND FORMATION; COPPER-CATALYZED REACTIONS; ENANTIOSELECTIVE; LEWIS ACID; ORGANOLITHIUM REAGENT;

EID: 84866245271     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201202251     Document Type: Article
Times cited : (33)

References (69)
  • 12
    • 84873982556 scopus 로고    scopus 로고
    • For a review, see
    • For a review, see
  • 16
    • 84873982070 scopus 로고    scopus 로고
    • For a review, see
    • For a review, see
  • 21
    • 84873981774 scopus 로고    scopus 로고
    • For general reviews, see
    • For general reviews, see
  • 27
    • 84873981997 scopus 로고    scopus 로고
    • For selected examples, see
    • For selected examples, see
  • 36
    • 84873982530 scopus 로고    scopus 로고
    • For selected examples, see
    • For selected examples, see
  • 58
    • 78650403767 scopus 로고    scopus 로고
    • For a recent review on the use of phosphoramidites as chiral ligands see:, J. F. Teichert, B. L. Feringa, Angew. Chem. 2010, 122, 2538
    • (2010) Angew. Chem. , vol.122 , pp. 2538
    • Teichert, J.F.1    Feringa, B.L.2
  • 60
    • 84873983750 scopus 로고    scopus 로고
    • 3 ·tBuOMe complex was tested in our system the starting material remained unaltered
    • 3 ·tBuOMe complex was tested in our system the starting material remained unaltered.
  • 62
    • 84873983629 scopus 로고    scopus 로고
    • N2) and conversion were both lower than the results obtained with organolithium reagents (see the Supporting Information)
    • N2) and conversion were both lower than the results obtained with organolithium reagents (see the Supporting Information).
  • 64
    • 56749083661 scopus 로고    scopus 로고
    • III species through π-bonding between the remaining halide and the metal center in the Cu-catalyzed AAA of 1,4-dihalo-2-butenes, see:, C. A. Falciola, A. Alexakis, Chem. Eur. J. 2008, 14, 10615.
    • (2008) Chem. Eur. J. , vol.14 , pp. 10615
    • Falciola, C.A.1    Alexakis, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.