From Spirolactam Mixtures to Regioisomerically Pure 5- and 6-Rhodamines: A Chemodosimeter-Inspired Strategy
Authors:
- 3 April 2012
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 14 (8) , 2014-2017
Abstract
Inspired by the ring-open reaction of rhodamine spriolactams as typical chemodosimeters, a general strategy is proposed to conveniently and efficiently synthesize isomerically pure 5- and 6-R-tetramethylrhodamine on a larger scale.Keywords
This publication has 27 references indexed in Scilit:
- Design, Synthesis, and Characterization of Fluorescent Cobalamin Analogues with High Quantum EfficienciesOrganic Letters, 2009
- Synthesis of 5- and 6-Carboxy-X-rhodaminesOrganic Letters, 2008
- Novel strategies for the site-specific covalent labelling of nucleic acidsChemical Communications, 2008
- Fluorescence based strategies for genetic analysisChemical Communications, 2005
- Cell-permeable small molecule probes for site-specific labeling of proteinsElectronic supplementary information (ESI) available: experimental details and characterization of compounds. See http://www.rsc.org/suppdata/cc/b3/b309196a/Chemical Communications, 2003
- Microwave-Assisted Syntheses of Regioisomerically Pure Bromorhodamine DerivativesOrganic Letters, 2003
- Optimizing primer–probe design for fluorescent PCRJournal of Neuroscience Methods, 2003
- Efficiencies of fluorescence resonance energy transfer and contact-mediated quenching in oligonucleotide probesNucleic Acids Research, 2002
- Spectral characterization of fluorescent 5-iodoacetamidotetramethylrhodamine and its N-acetylcysteine derivativePhysical Chemistry Chemical Physics, 1999
- Fluorescence polarization of skeletal muscle fibers labeled with rhodamine isomers on the myosin heavy chainBiophysical Journal, 1996