A convenient synthesis of new chromophoric tetracyanobutadiene-scaffolded peptides via a dipolar [2+2] cycloaddition–cycloreversion reaction ☆

[1]  Seulki Lee,et al.  Peptides and peptide hormones for molecular imaging and disease diagnosis. , 2010, Chemical reviews.

[2]  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.

[3]  F. Diederich,et al.  New donor-acceptor chromophores by formal [2+2] cycloaddition of donor-substituted alkynes to dicyanovinyl derivatives. , 2009, Organic & biomolecular chemistry.

[4]  J. Rao,et al.  Fluorescence imaging in vivo: recent advances. , 2007, Current opinion in biotechnology.

[5]  Apurba K. Das,et al.  A short water-soluble self-assembling peptide forms amyloid-like fibrils. , 2006, Chemical communications.

[6]  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.

[7]  Ivan Biaggio,et al.  A new class of organic donor-acceptor molecules with large third-order optical nonlinearities. , 2005, Chemical communications.

[8]  J. Howard,et al.  Requirement for an oxidant in Pd/Cu co-catalyzed terminal alkyne homocoupling to give symmetrical 1,4-disubstituted 1,3-diynes. , 2005, The Journal of organic chemistry.

[9]  C. Tung,et al.  Fluorescent peptide probes for in vivo diagnostic imaging , 2004, Biopolymers.

[10]  Luke G Green,et al.  A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. , 2002, Angewandte Chemie.

[11]  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.

[12]  M. G. Finn,et al.  Click Chemistry: Diverse Chemical Function from a Few Good Reactions. , 2001, Angewandte Chemie.

[13]  Diederich,et al.  Acetylenic Coupling: A Powerful Tool in Molecular Construction. , 2000, Angewandte Chemie.

[14]  C. Bertozzi,et al.  Cell surface engineering by a modified Staudinger reaction. , 2000, Science.

[15]  M. Aslam,et al.  Bioconjugation: Protein Coupling Techniques for the Biomedical Sciences , 1998 .

[16]  R. Liskamp,et al.  Solid‐Phase Syntheses of Peptoids using Fmoc‐Protected N‐Substituted Glycines: The Synthesis of (Retro)Peptoids of Leu‐Enkephalin and Substance P , 1998 .

[17]  K. Rose,et al.  Construction of protein analogues by site-specific condensation of unprotected fragments. , 1992, Bioconjugate chemistry.

[18]  A. S. Hay.  Oxidative Coupling of Acetylenes. II1 , 1962 .