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Volumn 1, Issue 12, 2003, Pages 2111-2119

Intramolecular carbolithiation reactions for the preparation of 3-alkenylpyrrolidines

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; CHROMATOGRAPHY; ETHERS; LITHIUM; MOLECULAR DYNAMICS; MOLECULAR STRUCTURE; OLEFINS; ORGANIC ACIDS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL); TIN;

EID: 0142010039     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b303670g     Document Type: Article
Times cited : (33)

References (44)
  • 32
    • 0342429300 scopus 로고
    • note
    • The stereoselectivity on cyclization of a methoxy-substituted organolithium species has been found to be dependent on the solvent system used, see: W. F. Bailey and X.-L. Jiang, J. Org. Chem., 1994, 59, 6528; for a cyclic substrate that gives predominantly the desired 3,4-cis substitution pattern after anionic cyclization, see Scheme 9, ref. 5a.
    • (1994) J. Org. Chem. , vol.59 , pp. 6528
    • Bailey, W.F.1    Jiang, X.-L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.