메뉴 건너뛰기




Volumn 51, Issue 38, 2012, Pages 9581-9586

Forming tertiary organolithiums and organocuprates from nitrile precursors and their bimolecular reactions with carbon electrophiles to form quaternary carbon stereocenters

Author keywords

diastereoselectivity; fragment coupling; fused ring systems; lithiation; terpenoids

Indexed keywords

DIASTEREO-SELECTIVITY; FRAGMENT-COUPLING; FUSED-RING SYSTEM; LITHIATION; TERPENOIDS;

EID: 84866434544     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201205001     Document Type: Article
Times cited : (22)

References (58)
  • 16
    • 0003961355 scopus 로고    scopus 로고
    • For a general review of reductive lithiation, see:, Pergamon, Oxford, .
    • For a general review of reductive lithiation, see:, J. Clayden, Organolithiums: Selectivity for Synthesis Pergamon, Oxford, 2002, pp. 149-165.
    • (2002) Organolithiums: Selectivity for Synthesis , pp. 149-165
    • Clayden, J.1
  • 36
    • 84873983055 scopus 로고    scopus 로고
    • Reference [7d]
    • Reference [7d].
  • 39
    • 84859700410 scopus 로고    scopus 로고
    • The use of a silyl chloride was required in order to achieve synthetically useful yields of the 1,4 adduct. For a discussion on the current understanding of the role of silyl chlorides in cuprate reactions and leading references, see.
    • The use of a silyl chloride was required in order to achieve synthetically useful yields of the 1,4 adduct. For a discussion on the current understanding of the role of silyl chlorides in cuprate reactions and leading references, see:, N. Yoshikai, E. Nakamura, Chem. Rev. 2012, 112, 2339.
    • (2012) Chem. Rev. , vol.112 , pp. 2339
    • Yoshikai, N.1    Nakamura, E.2
  • 42
    • 85005461637 scopus 로고
    • the stereochemistry of protonation and methylation of 4-tert-butyl-1-phenylcyclohexyllithium has been investigated, see.
    • the stereochemistry of protonation and methylation of 4-tert-butyl-1-phenylcyclohexyllithium has been investigated, see:, B. A. Keys, E. L. Eliel, E. Juristi, Isr. J. Chem. 1989, 29, 171.
    • (1989) Isr. J. Chem. , vol.29 , pp. 171
    • Keys, B.A.1    Eliel, E.L.2    Juristi, E.3
  • 51
    • 84873984608 scopus 로고    scopus 로고
    • H. Wang, P. Kohler, L. E. Overman, K. N. Houk, submitted
    • H. Wang, P. Kohler, L. E. Overman, K. N. Houk, submitted


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.