Efficient synthesis of rhodamine conjugates through the 2'-position

Bioorganic and Medicinal Chemistry Letters

Volumn 10, Issue 14, 2000, Pages 1539-1541

  Adamczyk, Maciej ^a   Grote, Jonathan ^a  

^a ABBOTT DIAGNOSTICS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; ESTER DERIVATIVE; RHODAMINE;

ARTICLE; CHEMICAL REACTION; CONJUGATE; STRUCTURE ANALYSIS; SYNTHESIS;

AMIDES; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DRUG DESIGN; ESTERS; INDICATORS AND REAGENTS; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; RHODAMINES; SPECTROMETRY, MASS, SECONDARY ION; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0034679643     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(00)00279-1     Document Type: Article

References (14)

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11. The structures of rhodamine 6G and rhodamine 123 (Aldrich) are referred to as rhodamine esters A and B (bottom of page 3) to be totally unambiguous. Rhodamines are named according to several different conventions depending on the source.
12. We have demonstrated ESMS to be a useful tool for studying reaction intermediates: see Adamczyk, M.; Fishpaugh, J.; Gebler, J.; Mattingly, P. G.; Shreder, K. Eur. Mass Spec. 1998, 4, 121.
13. +.
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