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Volumn 16, Issue 18, 2014, Pages 4904-4907

Total synthesis of aspeverin via an iodine(III)-mediated oxidative cyclization

Author keywords

[No Author keywords available]

Indexed keywords

ASPEVERIN; BIOLOGICAL PRODUCT; CARBAMIC ACID DERIVATIVE; INDOLE ALKALOID; IODINE;

EID: 84927582680     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol5024163     Document Type: Article
Times cited : (24)

References (54)
  • 19
    • 23044492191 scopus 로고    scopus 로고
    • Although not directly applicable in this context, intramolecular cyclizations of carbamates onto 2-thiophenyl substituted indoles have been reported: Feldman, K. S.; Vidulova, D. B.; Karatjas, A. G. J. Org. Chem. 2005, 70, 6429-6440.
    • (2005) J. Org. Chem. , vol.70 , pp. 6429-6440
    • Feldman, K.S.1    Vidulova, D.B.2    Karatjas, A.G.3
  • 20
    • 0000285539 scopus 로고
    • For examples of hypervalent iodine-mediated addition of nucleophiles to indoles, see: (a) Awang, D. V. C.; Vincent, A. Can. J. Chem. 1980, 58, 1589-1591.
    • (1980) Can. J. Chem. , vol.58 , pp. 1589-1591
    • Awang, D.V.C.1    Vincent, A.2
  • 37
    • 0039248532 scopus 로고
    • For representative examples of oxidation benzylic to the C-2 position of indoles, see: (a) Yoshida, K.; Goto, J.; Ban, Y. Chem. Pharm. Bull. 1987, 35, 4700-4704.
    • (1987) Chem. Pharm. Bull. , vol.35 , pp. 4700-4704
    • Yoshida, K.1    Goto, J.2    Ban, Y.3
  • 46
    • 35348822659 scopus 로고    scopus 로고
    • For a detailed analysis of the regioselectivity of Fischer indole syntheses within fused ring systems of varying stereochemistry, see: Diedrich, C. L.; Frey, W.; Christoffers, J. Eur. J. Org. Chem. 2007, 28, 4731-4737.
    • (2007) Eur. J. Org. Chem. , vol.28 , pp. 4731-4737
    • Diedrich, C.L.1    Frey, W.2    Christoffers, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.