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Volumn , Issue 12, 2002, Pages 1759-1774

From amino acids to Dihydrofurans: Functionalized allenes in modern organic synthesis

Author keywords

2,5 Dihydrofurans; Allenes; Amino acids; Gold catalysis; Organocopper reagents

Indexed keywords

ADDITION REACTIONS; AMINO ACIDS; DERIVATIVES; ION EXCHANGE RESINS; OXIDATION;

EID: 0036995522     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2002-33707     Document Type: Review
Times cited : (135)

References (104)
  • 19
    • 0345476898 scopus 로고    scopus 로고
    • (b) Evans, P. A.; Murthy, V. S.; Roseman, J. D.; Rheingold, A. L. Angew. Chem. Int. Ed. 1999, 38, 3175; Angew. Chem. 1999, 111, 3370.
    • (1999) Angew. Chem. , vol.111 , pp. 3370
  • 23
    • 0030902124 scopus 로고    scopus 로고
    • (a) Krause, N.; Gerold, A. Angew. Chem., Int. Ed. Engl. 1997, 36, 186; Angew. Chem. 1997, 109, 194.
    • (1997) Angew. Chem. , vol.109 , pp. 194
  • 27
    • 0016184254 scopus 로고
    • (a) Rando, R. R. Science 1974, 185, 320.
    • (1974) Science , vol.185 , pp. 320
    • Rando, R.R.1
  • 42
    • 0346395825 scopus 로고    scopus 로고
    • Ph.D. Thesis; Dortmund University: Germany
    • Canisius, J. Ph.D. Thesis; Dortmund University: Germany, 2000.
    • (2000)
    • Canisius, J.1
  • 46
    • 0030001023 scopus 로고    scopus 로고
    • Ref. 11
    • Attempts to prepare 2-en-4-ynoates with unprotected amino functions in 2-position by using the corresponding aminophosphonate failed: Seki, M.; Matsumoto, K. Synthesis 1996, 580. Ref. 11.
    • (1996) Synthesis , pp. 580
    • Seki, M.1    Matsumoto, K.2
  • 54
    • 0346395821 scopus 로고    scopus 로고
    • Unpublished results
    • The protonation of allenyl enolates bearing alkyl substituents at C-2 also occurs without diastereoselectivity: Krause, N. Unpublished results.
    • Krause, N.1
  • 66
    • 0019164421 scopus 로고
    • (a) Franck, B.; Gehrken, H.-P. Angew. Chem., Int. Ed. Engl. 1980, 19, 461; Angew. Chem. 1980, 92, 484.
    • (1980) Angew. Chem. , vol.92 , pp. 484
  • 73
    • 0345764796 scopus 로고    scopus 로고
    • Note
    • 26f
  • 75
    • 0346395818 scopus 로고    scopus 로고
    • Note
    • Without transmetalation of the lithium enolate to the less basic titanium enolate the only product obtained by treatment with the acetone soln of DMDO is the aldol adduct of the ester enolate with acetone.
  • 81
    • 0034600902 scopus 로고    scopus 로고
    • (b) For the corresponding gold-catalyzed cyclization allenyl ketones to furans see: Hashmi, A. S. K.; Schwarz, L.; Choi, J.-K.; Frost, T. M. Angew. Chem. Int. Ed. 2000, 39, 2285; Angew. Chem. 2000, 112, 2382.
    • (2000) Angew. Chem. , vol.112 , pp. 2382
  • 84
    • 0026628175 scopus 로고
    • and references cited therein
    • Syntheses of racemic citreoviral: (a) Ebenezer, W.; Pattenden, G. Tetrahedron Lett. 1992, 33, 4053; and references cited therein.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 4053
    • Ebenezer, W.1    Pattenden, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.