Fluorogenic click reaction Export

@article{citeulike:5978777, abstract = {Fluorogenic Cu(i)-catalyzed alkyne-azide cycloaddition (CuAAC) reactions have emerged as a powerful tool for bioconjugation, materials science, organic synthesis and drug discovery. This review highlights the design of the recent development of fluorogenic CuAAC reactions as well as their applications.}, author = {Droumaguet, Celine L. and Wang, Chao and Wang, Qian}, citeulike-article-id = {5978777}, citeulike-linkout-0 = {http://dx.doi.org/10.1039/b901975h}, citeulike-linkout-1 = {http://www.rsc.org/Publishing/Journals/article.asp?doi=b901975h}, doi = {10.1039/b901975h}, journal = {Chem. Soc. Rev.}, keywords = {click-chemistry, fluorogenic}, posted-at = {2009-10-21 07:12:17}, priority = {2}, publisher = {The Royal Society of Chemistry}, title = {Fluorogenic click reaction}, url = {http://dx.doi.org/10.1039/b901975h}, year = {2010} }

TY - JOUR ID - citeulike:5978777 L3 - citeulike-article-id:5978777 N2 - Fluorogenic Cu(i)-catalyzed alkyne-azide cycloaddition (CuAAC) reactions have emerged as a powerful tool for bioconjugation, materials science, organic synthesis and drug discovery. This review highlights the design of the recent development of fluorogenic CuAAC reactions as well as their applications. JF - Chem. Soc. Rev. TI - Fluorogenic click reaction PB - The Royal Society of Chemistry KW - click-chemistry KW - fluorogenic AU - Droumaguet, Celine AU - Wang, Chao AU - Wang, Qian PY - 2010/// UR - http://dx.doi.org/10.1039/b901975h ER -