메뉴 건너뛰기




Volumn 11, Issue 12, 2005, Pages 3502-3510

Multicomponent domino processes based on the organocatalytic generation of conjugated acetylides: Efficient synthetic manifolds for diversity-oriented molecular construction

Author keywords

Alkynes; Domino reactions; Heterocycles; Multicomponent reactions; Nitrogen

Indexed keywords

CATALYSIS; CATALYSTS; HALOGENATION; NITROGEN; STOICHIOMETRY; SYNTHESIS (CHEMICAL);

EID: 20444500603     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200401267     Document Type: Review
Times cited : (128)

References (86)
  • 1
    • 0001847186 scopus 로고    scopus 로고
    • (Eds.: M. Shibasaki, J. F. Stoddart, F. Vogtle), Wiley-VCH, Weinheim and references therein
    • a) L. F. Tietze, F. Haunert in Stimulating Concepts in Chemistry (Eds.: M. Shibasaki, J. F. Stoddart, F. Vogtle), Wiley-VCH, Weinheim, 2000, pp. 39-64;
    • (2003) Stimulating Concepts in Chemistry , pp. 39-64
    • Tietze, L.F.1    Haunert, F.2
  • 3
    • 0042745386 scopus 로고    scopus 로고
    • c) for an excellent review of recent advances in solution-phase multicomponent methodology for the synthesis of heterocycles: R. V. A. Orru, M. Greef, Synthesis 2003, 10, 1471-1499;
    • (2003) Synthesis , vol.10 , pp. 1471-1499
    • Orru, R.V.A.1    Greef, M.2
  • 5
    • 0001134412 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 3168-3210;
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3168-3210
  • 7
    • 0038637120 scopus 로고    scopus 로고
    • For a recent example of this concept in the phosphine-catalyzed addition of alcohols to activated olefins, see: I. C. Stewart, R. G. Bergman, F. D. Toste, J. Am. Chem. Soc. 2003, 125, 8696-8697.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 8696-8697
    • Stewart, I.C.1    Bergman, R.G.2    Toste, F.D.3
  • 11
    • 0033577829 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1999, 38, 1463-1465;
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 1463-1465
  • 13
    • 0037119338 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 3054-3056;
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 3054-3056
  • 16
    • 0035648364 scopus 로고    scopus 로고
    • f) E. M. Carreira, Chimia 2001, 55, 818-820;
    • (2001) Chimia , vol.55 , pp. 818-820
    • Carreira, E.M.1
  • 31
    • 0003417469 scopus 로고
    • (Eds.: B. M. Trost, I. Fleming, M. F. Semmelhack), Pergamon, Oxford
    • c) M. E. Jung, in Comprehensive Organic Synthesis, (Eds.: B. M. Trost, I. Fleming, M. F. Semmelhack), Pergamon, Oxford, 1991;
    • (1991) Comprehensive Organic Synthesis
    • Jung, M.E.1
  • 33
    • 0010338666 scopus 로고
    • a) For a review including the seminal work of Winterfeldt, see: E. Winterfeldt, Angew. Chem. 1967, 79, 389;
    • (1967) Angew. Chem. , vol.79 , pp. 389
    • Winterfeldt, E.1
  • 38
    • 0034867881 scopus 로고    scopus 로고
    • and references therein
    • e) X. Lu, C. Zhang. Z. Xu, Acc. Chem. Res. 2001, 34, 535-544, and references therein;
    • (2001) Acc. Chem. Res. , vol.34 , pp. 535-544
    • Lu, X.1    Zhang, C.2    Xu, Z.3
  • 40
  • 41
    • 11944259320 scopus 로고    scopus 로고
    • and references therein
    • b) for an excellent discussion on the difference between the tandem Michael aldol reactions on terminal conjugated alkynes and the Morita-Baylis-Hillman reaction, see: T. Kataoka, H. Kinoshita, Eur. J. Org. Chem. 2005, 45-58, and references therein.
    • (2005) Eur. J. Org. Chem. , pp. 45-58
    • Kataoka, T.1    Kinoshita, H.2
  • 42
    • 2442629288 scopus 로고    scopus 로고
    • For selected examples of organocatalytic conjugated addition to conjugated terminal alkynes, see: a) M. Bella, K. A. Jørgensen, J. Am. Chem. Soc. 2004, 126, 5672-5673;
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 5672-5673
    • Bella, M.1    Jørgensen, K.A.2
  • 48
    • 20444505598 scopus 로고    scopus 로고
    • For synthesis and interesting comments about these aromatic units, see: L. A. Paquette, Chemtracts 2002, 15, 335-366.
    • (2002) Chemtracts , vol.15 , pp. 335-366
    • Paquette, L.A.1
  • 56
    • 0034697199 scopus 로고    scopus 로고
    • a) For an excellent review on synthesis of vicinal amino alcohols including many naturally occurring and biologically relevant compounds, see: S. C. Bergmeier, Tetrahedron 2000, 56, 2561-2576;
    • (2000) Tetrahedron , vol.56 , pp. 2561-2576
    • Bergmeier, S.C.1
  • 57
    • 0242500412 scopus 로고    scopus 로고
    • b) for a review on synthesis and biological activities of long chain 2-amino alcohols, see: V. Constantinou-Kokotou, Lett. Pept. Sci. 2002, 9, 143-152.
    • (2002) Lett. Pept. Sci. , vol.9 , pp. 143-152
    • Constantinou-Kokotou, V.1
  • 58
    • 0037201534 scopus 로고    scopus 로고
    • a) For a recent review on β-substituted β-amino acids synthesis, see: M. Liu, M. P. Sibi, Tetrahedron 2002, 58, 7991-8035;
    • (2002) Tetrahedron , vol.58 , pp. 7991-8035
    • Liu, M.1    Sibi, M.P.2
  • 72
  • 73
    • 0035909591 scopus 로고    scopus 로고
    • for recent examples from preformed scaffolds
    • b) R. U. Braun, K. Zeitler, T. J. J. Muller, Org. Lett. 2001, 3, 3297-3300; for recent examples from preformed scaffolds:
    • (2001) Org. Lett. , vol.3 , pp. 3297-3300
    • Braun, R.U.1    Zeitler, K.2    Muller, T.J.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.