New photocleavable linker: α-thioacetophenone-type linker.

[1]  Peng Wu,et al.  Single-stranded DNA as a cleavable linker for bioorthogonal click chemistry-based proteomics. , 2013, Bioconjugate chemistry.

[2]  S. Verhelst,et al.  Cleavable trifunctional biotin reagents for protein labelling, capture and release. , 2013, Chemical communications.

[3]  Kam Y. J. Zhang,et al.  CDC25A-inhibitory RE derivatives bind to pocket adjacent to the catalytic site. , 2013, Molecular bioSystems.

[4]  B. Kuster,et al.  A Simple and Effective Cleavable Linker for Chemical Proteomics Applications* , 2012, Molecular & Cellular Proteomics.

[5]  F. Dekker,et al.  A photocleavable affinity tag for the enrichment of alkyne-modified biomolecules , 2012 .

[6]  Alain Wagner,et al.  Cleavable linkers in chemical biology. , 2012, Bioorganic & medicinal chemistry.

[7]  S. Copley,et al.  A dimethyl ketal-protected benzoin-based linker suitable for photolytic release of unprotected peptides. , 2011, The Journal of organic chemistry.

[8]  M. Damha,et al.  New light labile linker for solid phase synthesis of 2'-O-acetalester oligonucleotides and applications to siRNA prodrug development. , 2011, Bioorganic & medicinal chemistry letters.

[9]  A. Levitzki,et al.  Novel method for the synthesis of urea backbone cyclic peptides using new Alloc‐protected glycine building units , 2010, Journal of peptide science : an official publication of the European Peptide Society.

[10]  S. Sieber,et al.  A photolabile linker for the mild and selective cleavage of enriched biomolecules from solid support. , 2009, The Journal of organic chemistry.

[11]  J. Shabanowitz,et al.  Enrichment and Site Mapping of O-Linked N-Acetylglucosamine by a Combination of Chemical/Enzymatic Tagging, Photochemical Cleavage, and Electron Transfer Dissociation Mass Spectrometry* , 2009, Molecular & Cellular Proteomics.

[12]  Bin Chen,et al.  Functional differences in epigenetic modulators-superiority of mercaptoacetamide-based histone deacetylase inhibitors relative to hydroxamates in cortical neuron neuroprotection studies. , 2007, Journal of medicinal chemistry.

[13]  Günter Mayer,et al.  Biologically active molecules with a "light switch". , 2006, Angewandte Chemie.

[14]  Yanguang Wang,et al.  Phenacyl esters as a new photocleavable linker in liquid-phase chemistry , 2005 .

[15]  D. Enders,et al.  A triazene-based new photolabile linker in solid phase chemistry , 2004 .

[16]  B. Cravatt,et al.  Activity-based protein profiling: the serine hydrolases. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[17]  E. Vedejs,et al.  Characterization of monomeric thiopivalaldehyde , 1986 .

[18]  E. Vedejs,et al.  Total synthesis of carbocyclic cytochalasans , 1984 .

[19]  E. Vedejs,et al.  A method for mild photochemical oxidation; conversion of phenacyl sulfides into carbonyl compounds , 1984 .

[20]  A. Brandt,et al.  SYNTHESIS OF A NOVEL CLASS OF 2‐AZETIDINONES‐ 4‐THIOXO‐2‐AZETIDINONES. CONVERSION TO A 1,2‐SECO‐5,6‐DEHYDROPENICILLIN , 1976 .

[21]  A. Padwa,et al.  Photoelimination of a .beta.-oxo sulfide with a low-lying .pi.-.pi.* triplet state , 1971 .

[22]  R. Woodward,et al.  Photosensitive protecting groups , 1970 .

[23]  M. Caserio,et al.  Ketonization of enols in aprotic solvents. Photoelimination of .beta.-keto sulfides , 1970 .

[24]  M. Joullié,et al.  Effect of Structure on Reactivity. IX. A Study of the Aminolysis of Esters of Trichloro- and Trifluoroacetic Acids , 1954 .

[25]  J. Raleigh,et al.  Synthesis and reactions of thioaldehyde dehydropeptides related to β-lactam antibiotics , 1974 .

[26]  C. Reese,et al.  A photo-induced rearrangement involving aryl participation , 1962 .

[27]  R. Pepinsky,et al.  X-ray analysis of the structure of gelsemine hydrohalides , 1959 .