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Volumn 69, Issue 36, 2013, Pages 7683-7691

Template-induced macrocycle diversity through large ring-forming alkylations of tryptophan

Author keywords

Diversity; Friedel Crafts; Macrocycle; NMR solution structure; Peptidomimetic

Indexed keywords

LEWIS ACID; MACROCYCLIC COMPOUND; TRYPTOPHAN;

EID: 84880917212     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.05.060     Document Type: Article
Times cited : (26)

References (111)
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    • A possible, though less likely in our opinion, path from 5 to 6 under these conditions would involve the transient formation of a branched aryl allylic ether that subsequently undergoes acid-promoted sigmatropic rearrangement
    • A possible, though less likely in our opinion, path from 5 to 6 under these conditions would involve the transient formation of a branched aryl allylic ether that subsequently undergoes acid-promoted sigmatropic rearrangement. U. Svanholm, and V.D. Parker J. Chem. Soc; Perkin Trans. 2 1974 169 173
    • (1974) J. Chem. Soc; Perkin Trans. 2 , pp. 169-173
    • Svanholm, U.1    Parker, V.D.2
  • 96
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    • For synthesis of C-3 allylated pyrroloindolines see
    • L.L. Anka-Lufford, M.R. Prinsell, and D.J. Weix J. Org. Chem. 77 2012 9989 10000 For synthesis of C-3 allylated pyrroloindolines see
    • (2012) J. Org. Chem. , vol.77 , pp. 9989-10000
    • Anka-Lufford, L.L.1    Prinsell, M.R.2    Weix, D.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.