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Volumn 42, Issue 45, 2003, Pages 5625-5629

Studies Directed toward the Total Synthesis of Lactonamycin: Control of the Sense of Cycloaddition of a Quinone through Directed Intramolecular Catalysis

Author keywords

Antibiotics; Diels Alder reaction; Natural products; Quinones; Total synthesis

Indexed keywords

CATALYSIS; ISOMERS; SYNTHESIS (CHEMICAL);

EID: 0344360724     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200352591     Document Type: Article
Times cited : (43)

References (26)
  • 4
    • 0034597522 scopus 로고    scopus 로고
    • For synthetic and model studies toward the synthesis of lactonamycin, see: a) C. Cox, S. J. Danishefsky, Org. Lett. 2000, 2, 3493-3496;
    • (2000) Org. Lett. , vol.2 , pp. 3493-3496
    • Cox, C.1    Danishefsky, S.J.2
  • 9
    • 0344792636 scopus 로고    scopus 로고
    • T. Siu, C. D. Cox, S. J. Danishefsky, Angew. Chem. 2003, 115, 5787-5792; Angew. Chem. Int. Ed. 2003, 42, 5629-5634.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 5629-5634
  • 12
    • 0002403154 scopus 로고
    • for a related use of this concept in juglone and naphthazarin systems, see: b) V. H. Powell, A.J. Birch, Tetrahedron Lett. 1970, 11, 3467-3469;
    • (1970) Tetrahedron Lett. , vol.11 , pp. 3467-3469
    • Powell, V.H.1    Birch, A.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.