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Volumn 133, Issue 15, 2011, Pages 5798-5801

Total synthesis of N-methylwelwitindolinone D isonitrile

Author keywords

[No Author keywords available]

Indexed keywords

ARYLATION REACTIONS; ENOLATES; INDOLE ALKALOIDS; ISONITRILES; ISOTHIOCYANATES; LEWIS ACID; NATURAL PRODUCTS; TOTAL SYNTHESIS;

EID: 79954562814     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja201834u     Document Type: Article
Times cited : (85)

References (46)
  • 26
    • 27644566322 scopus 로고    scopus 로고
    • Two elegant syntheses of 1, the unique, cyclobutane-containing member of the family, have been reported. See
    • Two elegant syntheses of 1, the unique, cyclobutane-containing member of the family, have been reported. See: Baran, P. S.; Richter, J. M. J. Am. Chem. Soc. 2005, 127, 15394-15396
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 15394-15396
    • Baran, P.S.1    Richter, J.M.2
  • 35
    • 0001123717 scopus 로고
    • Compound 10b was prepared in four steps (76% yield) from commercially available 2-bromo-6-nitrotoluene. See
    • Compound 10b was prepared in four steps (76% yield) from commercially available 2-bromo-6-nitrotoluene. See: Maehr, H; Smallheer, J. M. J. Org. Chem. 1981, 46, 1752-1755
    • (1981) J. Org. Chem. , vol.46 , pp. 1752-1755
    • Maehr, H.1    Smallheer, J.M.2
  • 36
    • 79954506677 scopus 로고    scopus 로고
    • Reference 5h.
    • Reference 5h.
  • 38
    • 0021672373 scopus 로고
    • For examples of α-arylation of β-ketoaldehydes using stoichiometric organometallic reagents, see
    • For examples of α-arylation of β-ketoaldehydes using stoichiometric organometallic reagents, see: Collins, D. J.; Cullen, J. D.; Fallon, G. D.; Gatehouse, B. M. Aust. J. Chem. 1984, 37, 2279-2294
    • (1984) Aust. J. Chem. , vol.37 , pp. 2279-2294
    • Collins, D.J.1    Cullen, J.D.2    Fallon, G.D.3    Gatehouse, B.M.4
  • 40
    • 84951531840 scopus 로고
    • For additional examples employing DMDO to prepare 3-hydroxy oxindoles directly from indoles, see
    • For additional examples employing DMDO to prepare 3-hydroxy oxindoles directly from indoles, see: Zhang, X.; Foote, C. S. J. Am. Chem. Soc. 1993, 115, 8867-8868
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 8867-8868
    • Zhang, X.1    Foote, C.S.2
  • 43
    • 79954511306 scopus 로고    scopus 로고
    • Yield based on a two-step procedure: see ref 15a.
    • Yield based on a two-step procedure: see ref 15a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.