메뉴 건너뛰기




Volumn 12, Issue 22, 2010, Pages 5210-5213

Synthesis of the enantiomer of the structure assigned to the natural product nobilisitine A

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; BIOLOGICAL PRODUCT; FUSED HETEROCYCLIC RINGS; NOBILISITINE A;

EID: 78449295979     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol102249q     Document Type: Article
Times cited : (33)

References (21)
  • 5
    • 78449308657 scopus 로고    scopus 로고
    • For reviews on methods for generating compounds such as 4 by microbial dihydroxylation of the corresponding aromatics, as well as the synthetic applications of these metabolites, see
    • For reviews on methods for generating compounds such as 4 by microbial dihydroxylation of the corresponding aromatics, as well as the synthetic applications of these metabolites, see
  • 13
    • 78449269740 scopus 로고    scopus 로고
    • For a related reduction process involving Raney cobalt, see
    • For a related reduction process involving Raney cobalt, see
  • 15
    • 78449280562 scopus 로고    scopus 로고
    • For relevant examples of nitrogen-centered radical cyclization processes, see, for example
    • For relevant examples of nitrogen-centered radical cyclization processes, see, for example
  • 20
    • 78449311152 scopus 로고    scopus 로고
    • CCDC 793455 contains the supplementary crystallographic data for compound ent - . These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via
    • CCDC 793455 contains the supplementary crystallographic data for compound ent-1. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.