A convenient [2+2] cycloaddition–cycloreversion reaction for the synthesis of 1,1-dicyanobuta-1,3-diene-scaffolded peptides as new imaging chromophores
暂无分享,去创建一个
[1] C. Tung,et al. Developing visible fluorogenic 'click-on' dyes for cellular imaging. , 2011, Bioconjugate chemistry.
[2] F. Diederich,et al. A convenient synthesis of new chromophoric tetracyanobutadiene-scaffolded peptides via a dipolar [2+2] cycloaddition–cycloreversion reaction ☆ , 2011 .
[3] S. Bag,et al. Installation/modulation of the emission response via click reaction. , 2011, The Journal of organic chemistry.
[4] Seulki Lee,et al. Peptides and peptide hormones for molecular imaging and disease diagnosis. , 2010, Chemical reviews.
[5] Q. Wang,et al. Fluorogenic click reaction. , 2010, Chemical Society reviews.
[6] F. Diederich,et al. Mechanistic investigation of the dipolar [2+2] cycloaddition-cycloreversion reaction between 4-(N,N-dimethylamino)phenylacetylene and arylated 1,1-dicyanovinyl derivatives to form intramolecular charge-transfer chromophores. , 2010, Chemistry.
[7] F. Diederich,et al. New donor-acceptor chromophores by formal [2+2] cycloaddition of donor-substituted alkynes to dicyanovinyl derivatives. , 2009, Organic & biomolecular chemistry.
[8] Morten Meldal,et al. Cu-catalyzed azide-alkyne cycloaddition. , 2008, Chemical reviews.
[9] F. Diederich,et al. 1,2,3-triazoles as conjugative pi-linkers in push-pull chromophores: importance of substituent positioning on intramolecular charge-transfer. , 2008, Organic letters.
[10] J. Rao,et al. Fluorescence imaging in vivo: recent advances. , 2007, Current opinion in biotechnology.
[11] F. Diederich,et al. Donor-substituted 1,1,4,4-tetracyanobutadienes (TCBDS): new chromophores with efficient intramolecular charge-transfer interactions by atom-economic synthesis. , 2006, Chemistry.
[12] Ivan Biaggio,et al. A new class of organic donor-acceptor molecules with large third-order optical nonlinearities. , 2005, Chemical communications.
[13] Arwin J. Brouwer,et al. Efficient microwave-assisted synthesis of multivalent dendrimeric peptides using cycloaddition reaction (click) chemistry. , 2005, Chemical communications.
[14] C. Fahrni,et al. A Fluorogenic Probe for the Copper(I)-Catalyzed Azide−Alkyne Ligation Reaction: Modulation of the Fluorescence Emission via 3(n,π*)−1(π,π*) Inversion , 2004 .
[15] C. Tung,et al. Fluorescent peptide probes for in vivo diagnostic imaging , 2004, Biopolymers.
[16] A. Hallberg,et al. Design and synthesis of dihydrofolate reductase inhibitors encompassing a bridging ester group. Evaluation in a mouse colitis model. , 2003, Journal of medicinal chemistry.
[17] Luke G Green,et al. A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. , 2002, Angewandte Chemie.
[18] Morten Meldal,et al. Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(i)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. , 2002, The Journal of organic chemistry.
[19] M. Aslam,et al. Bioconjugation: Protein Coupling Techniques for the Biomedical Sciences , 1998 .
[20] D. Luna,et al. Knoevenagel condensation in the heterogeneous phase using aluminum phosphate-aluminum oxide as a new catalyst , 1984 .
[21] D. Luna,et al. Knoevenagel condensation in the heterogeneous phase using AlPO4-Al2O3 as a new catalyst , 1984 .