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Volumn , Issue 12, 2005, Pages 2015-2021

Synthesis of macrocyclic scaffolds from natural products and their utilization for solid-phase chemistry

Author keywords

Combinatorial chemistry; Natural products; Solid phase synthesis

Indexed keywords

CHEMISTRY; SCAFFOLDS; SOLIDS;

EID: 23744472085     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-869969     Document Type: Article
Times cited : (6)

References (18)
  • 12
    • 33645204410 scopus 로고    scopus 로고
    • note
    • (b) Compound 1 was produced in-house by a fungal strain in a 3000 L fermentor containing 2500 L of culture broth with an average titer of 85 mg/L.
  • 16
    • 33645203833 scopus 로고    scopus 로고
    • note
    • 2O as acid catalyst. The crystallographic data (excluding structure factors) for the structure of this compound have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 262678. Copies of the data can be obtained free of charge on application to CCDC 12 Union Road Cambridge CB2 1 EZ UK [fax: +44 (1223)336033 or email: deposit@ccdc.cam.ac.uk]
  • 17
    • 33645192132 scopus 로고    scopus 로고
    • note
    • PS-Merrifield resin (crosslinked with 1% 14-divinyl-benzene) diameter: 200 μm loading: 1.9 mmol/g.
  • 18
    • 33645209613 scopus 로고    scopus 로고
    • note
    • 2O (5:84:10:1). The composition of 8 and 9 was determined by quantitative HPLC of the cleavage solution without prior evaporation. Under these conditions the TEOC group is stable.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.