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Volumn 15, Issue 37, 2009, Pages 9417-9423

2,6,8-Irisubstituted 3-Hydroxychromone derivatives as fluorophores for live-cell imaging

Author keywords

Cellular imaging; Excited state intramolecular proton transfer (esipt); Fluorescence; Fluorophores; Hydroxychromones

Indexed keywords

CELLULAR ENVIRONMENT; CELLULAR IMAGING; CHARACTERISATION; EXCITED-STATE INTRAMOLECULAR PROTON TRANSFER (ESIPT); FLUORESCENCE PROPERTIES; FLUORESCENCE QUANTUM YIELD; HELA CELL; HYDROXYCHROMONES; HYDROXYL GROUPS; LIVE-CELL IMAGING; MOLAR EXTINCTION COEFFICIENT; PHOTOPHYSICAL;

EID: 70349300136     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200900279     Document Type: Article
Times cited : (28)

References (37)
  • 28
    • 70349268384 scopus 로고    scopus 로고
    • The use of a strong aqueous base (60%) is essential for the reaction.
    • The use of a strong aqueous base (60%) is essential for the reaction.
  • 29
    • 70349276030 scopus 로고    scopus 로고
    • The Sonogashira coupling with 11 a, b requires at least 4equiv of propargylamine since attempts using 2 equiv were performed without any product formation. Further, compound 12 b was formed from the 6,8-dibromochromone lib in low yields (16%) due to formation of the undesired disubstituted product.
    • The Sonogashira coupling with 11 a, b requires at least 4equiv of propargylamine since attempts using 2 equiv were performed without any product formation. Further, compound 12 b was formed from the 6,8-dibromochromone lib in low yields (16%) due to formation of the undesired disubstituted product.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.