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Volumn 43, Issue 15, 2004, Pages 1998-2001

Synthesis of the furanosteroidal antibiotic viridin

Author keywords

Cyclotrimerization; Dihydroxylation; Electrocyclic reactions; Inhibitors; Natural products

Indexed keywords

CATALYSIS; HYDROXYLATION; RHODIUM; SYNTHESIS (CHEMICAL);

EID: 3042823529     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200353129     Document Type: Article
Times cited : (114)

References (51)
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    • The reactive natural product (-)-FR182877 was recently discovered to be a potent and selective covalent inhibitor of carboxylesterase-1: G. C. Adam, C. D. Vanderwal, E. J. Sorensen, B. F. Cravatt, Angew. Chem. 2003, 115, 5638-5642; Angew. Chem. Int. Ed. 2003, 42, 5480-5484.
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  • 9
    • 0344413531 scopus 로고    scopus 로고
    • The reactive natural product (-)-FR182877 was recently discovered to be a potent and selective covalent inhibitor of carboxylesterase-1: G. C. Adam, C. D. Vanderwal, E. J. Sorensen, B. F. Cravatt, Angew. Chem. 2003, 115, 5638-5642; Angew. Chem. Int. Ed. 2003, 42, 5480-5484.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 5480-5484
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    • 0037121440 scopus 로고    scopus 로고
    • a) T. Mizutani, S. Honzawa, S.-y. Tosaki, M. Shibasaki, Angew. Chem. 2002, 114, 4874-4876; Angew. Chem. Int. Ed. 2002, 41, 4680-4682;
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 4680-4682
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    • 0001083027 scopus 로고
    • For reviews of metal-catalyzed cyclotrimerizations, see: a) K. P. C. Vollhardt, Angew. Chem. 1984, 96, 525-541; Angew. Chem. Int. Ed. Engl. 1984, 23, 539-556;
    • (1984) Angew. Chem. , vol.96 , pp. 525-541
    • Vollhardt, K.P.C.1
  • 32
    • 84985571853 scopus 로고
    • For reviews of metal-catalyzed cyclotrimerizations, see: a) K. P. C. Vollhardt, Angew. Chem. 1984, 96, 525-541; Angew. Chem. Int. Ed. Engl. 1984, 23, 539-556;
    • (1984) Angew. Chem. Int. Ed. Engl. , vol.23 , pp. 539-556
  • 37
    • 0019125839 scopus 로고
    • for cobalt-catalyzed cyclotrimerization applied to steroid synthesis, see: f) R. L. Funk, K. P. C. Vollhardt, J. Am. Chem. Soc. 1980, 102, 5253-5261;
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 5253-5261
    • Funk, R.L.1    Vollhardt, K.P.C.2
  • 39
    • 4544325392 scopus 로고    scopus 로고
    • note
    • 2, room temperature, 30 min, 100%.
  • 41
    • 4544339118 scopus 로고    scopus 로고
    • note
    • 3SiCl (1 equiv), -78 °C→RT, 10 h, 92%;
  • 42
    • 4544286501 scopus 로고    scopus 로고
    • note
    • 3 (1.0 equiv), reflux, 24 h, 90%. LDA = lithium diisopropylamide; DME = 1,2-dimethoxyethane.
  • 48
    • 0000785058 scopus 로고    scopus 로고
    • b) A. Fürstner, Angew. Chem. 2000, 112, 3140-3172; Angew. Chem. Int. Ed. 2000, 39, 3012-3043.
    • (2000) Angew. Chem. , vol.112 , pp. 3140-3172
    • Fürstner, A.1
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    • 0001399412 scopus 로고    scopus 로고
    • b) A. Fürstner, Angew. Chem. 2000, 112, 3140-3172; Angew. Chem. Int. Ed. 2000, 39, 3012-3043.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3012-3043


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.