메뉴 건너뛰기




Volumn 42, Issue 43, 2003, Pages 5358-5360

Catalysis-Based Total Synthesis of Latrunculin B

Author keywords

Alkynes; Cross coupling; Macrocycles; Metathesis; Natural products

Indexed keywords

BIOCHEMISTRY; CATALYSIS; CHEMICAL BONDS; SYNTHESIS (CHEMICAL);

EID: 0344875684     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200352413     Document Type: Article
Times cited : (137)

References (55)
  • 2
    • 0344008063 scopus 로고    scopus 로고
    • b) K.-S. Yeung, I. Paterson, Angew. Chem. 2002, 114, 4826-4847; Angew. Chem. Int. Ed. 2002, 41, 4632-4653.
    • (2002) Angew. Chem. , vol.114 , pp. 4826-4847
    • Yeung, K.-S.1    Paterson, I.2
  • 3
    • 0037122039 scopus 로고    scopus 로고
    • b) K.-S. Yeung, I. Paterson, Angew. Chem. 2002, 114, 4826-4847; Angew. Chem. Int. Ed. 2002, 41, 4632-4653.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 4632-4653
  • 6
    • 0031604152 scopus 로고    scopus 로고
    • c) Molecular Motors and the Cytoskeleton, Part B: K. Ayscough, Methods Enzymol. 1998, 298, 18-25;
    • (1998) Methods Enzymol. , vol.298 , pp. 18-25
    • Ayscough, K.1
  • 22
    • 0000775011 scopus 로고    scopus 로고
    • a) A. Fürstner, G. Seidel, Angew. Chem. 1998, 110, 1758-1760; Angew. Chem. Int. Ed. 1998, 37, 1734-1736;
    • (1998) Angew. Chem. , vol.110 , pp. 1758-1760
    • Fürstner, A.1    Seidel, G.2
  • 23
    • 0038731101 scopus 로고    scopus 로고
    • a) A. Fürstner, G. Seidel, Angew. Chem. 1998, 110, 1758-1760; Angew. Chem. Int. Ed. 1998, 37, 1734-1736;
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1734-1736
  • 31
  • 32
    • 0037083916 scopus 로고    scopus 로고
    • b) A. Fürstner, A. Leitner, Angew. Chem. 2002, 114, 632-635; Angew. Chem. Int. Ed. 2002, 41, 609-612;
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 609-612
  • 33
  • 34
    • 0037455149 scopus 로고    scopus 로고
    • c) A. Fürstner, A. Leitner, Angew. Chem. 2003, 115, 320-323; Angew. Chem. Int. Ed. 2003, 42, 308-311.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 308-311
  • 35
    • 0000689303 scopus 로고
    • For Fe-catalyzed reactions of alkenyl halides, see: a) M. Tamura, J. K. Kochi, J. Am. Chem. Soc. 1971, 93, 1487-1489;
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 1487-1489
    • Tamura, M.1    Kochi, J.K.2
  • 48
    • 0000785058 scopus 로고    scopus 로고
    • This must be seen in light of the fact that steric hindrance close to a double bond can be a significant obstacle in conventional alkene metathesis; the same pertains to sulfur-containing compounds, which are usually highly problematic in alkene metathesis. For a Review, see: A. Fürstner, Angew. Chem. 2000, 112, 3140-3172; Angew. Chem. Int. Ed. 2000, 39, 3012-3043; see also: S. J. Connon, S. Blechert, Angew. Chem. 2003, 115, 1944-1968; Angew. Chem. Int. Ed. 2003, 42, 1900-1923.
    • (2000) Angew. Chem. , vol.112 , pp. 3140-3172
    • Fürstner, A.1
  • 49
    • 0001399412 scopus 로고    scopus 로고
    • This must be seen in light of the fact that steric hindrance close to a double bond can be a significant obstacle in conventional alkene metathesis; the same pertains to sulfur-containing compounds, which are usually highly problematic in alkene metathesis. For a Review, see: A. Fürstner, Angew. Chem. 2000, 112, 3140-3172; Angew. Chem. Int. Ed. 2000, 39, 3012-3043; see also: S. J. Connon, S. Blechert, Angew. Chem. 2003, 115, 1944-1968; Angew. Chem. Int. Ed. 2003, 42, 1900-1923.
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 3012-3043
  • 50
    • 0038567454 scopus 로고    scopus 로고
    • This must be seen in light of the fact that steric hindrance close to a double bond can be a significant obstacle in conventional alkene metathesis; the same pertains to sulfur-containing compounds, which are usually highly problematic in alkene metathesis. For a Review, see: A. Fürstner, Angew. Chem. 2000, 112, 3140-3172; Angew. Chem. Int. Ed. 2000, 39, 3012-3043; see also: S. J. Connon, S. Blechert, Angew. Chem. 2003, 115, 1944-1968; Angew. Chem. Int. Ed. 2003, 42, 1900-1923.
    • (2003) Angew. Chem. , vol.115 , pp. 1944-1968
    • Connon, S.J.1    Blechert, S.2
  • 51
    • 0038215596 scopus 로고    scopus 로고
    • This must be seen in light of the fact that steric hindrance close to a double bond can be a significant obstacle in conventional alkene metathesis; the same pertains to sulfur-containing compounds, which are usually highly problematic in alkene metathesis. For a Review, see: A. Fürstner, Angew. Chem. 2000, 112, 3140-3172; Angew. Chem. Int. Ed. 2000, 39, 3012-3043; see also: S. J. Connon, S. Blechert, Angew. Chem. 2003, 115, 1944-1968; Angew. Chem. Int. Ed. 2003, 42, 1900-1923.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 1900-1923


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.