Traceless Staudinger Ligation for Bioconjugation of RNA

2021 ◽  
Vol 1 (2) ◽  
Author(s):  
Camélia Kitoun ◽  
Matthieu Fonvielle ◽  
Michel Arthur ◽  
Mélanie Etheve‐Quelquejeu ◽  
Laura Iannazzo
Keyword(s):  
Staudinger Ligation

ChemInform Abstract: Synthesis of Benzoate-Functionalized Phosphanes as Novel Building Blocks for the Traceless Staudinger Ligation.

ChemInform ◽  
2010 ◽  
Vol 41 (8) ◽  
Author(s):  
Constantin Mamat ◽  
Anke Flemming ◽  
Martin Koeckerling ◽  
Joerg Steinbach ◽  
Frank R. Wuerst
Keyword(s):  
Building Blocks ◽  
Staudinger Ligation

Recent progress using the Staudinger ligation for radiolabeling applications

2018 ◽  
Vol 61 (3) ◽  
pp. 165-178 ◽  
Author(s):  
Constantin Mamat ◽  
Matthew Gott ◽  
Jörg Steinbach
Keyword(s):  
Recent Progress ◽  
Staudinger Ligation

Stereoselective N-Glycosylation by Staudinger Ligation

2004 ◽  
Vol 6 (24) ◽  
pp. 4479-4482 ◽  
Author(s):  
Yi He ◽  
Ronald J. Hinklin ◽  
Jiyoung Chang ◽  
Laura L. Kiessling
Keyword(s):  
Staudinger Ligation

Site-Selective Protein Immobilization by Staudinger Ligation

2006 ◽  
Vol 45 (9) ◽  
pp. 1408-1412 ◽  
Author(s):  
Anja Watzke ◽  
Maja Köhn ◽  
Marta Gutierrez-Rodriguez ◽  
Ron Wacker ◽  
Hendrik Schröder ◽  
...  
Keyword(s):  
Protein Immobilization ◽  
Staudinger Ligation ◽  
Site Selective

Functional Group Interconversion

2015 ◽  
Author(s):  
Tristan H. Lambert
Keyword(s):  
Carboxylic Acid ◽  
High Yield ◽  
Staudinger Ligation ◽  
University Of Alberta ◽  
University Of Tennessee ◽  
University Of British Columbia ◽  
National University ◽  
Seoul National University ◽  
Oxidative Amidation ◽  
The University

Glenn M. Samm is at the University of British Columbia reported (Angew. Chem. Int. Ed. 2012, 51, 10804) the photofluorodecarboxylation of aryloxyacids such as 1 using Selectfluor 2. Jean-François Paquin at the Université Laval found (Org. Lett. 2012, 14, 5428) that the halogenation of alcohols (e.g., 4 to 5) could be achieved with [Et2NSF2]BF4 (XtalFluor-E) in the presence of the appropriate tetraethylammonium halide. A method for the reductive bromination of carboxylic acid 6 to bromide 7 was developed (Org. Lett. 2012, 14, 4842) by Norio Sakai at the Tokyo University of Science. Professor Sakai also reported (Org. Lett. 2012, 14, 4366) a related method for the reductive coupling of acid 8 with octanethiol to produce thioether 9. The esterification of primary alcohols in water-containing solvent was achieved (Org. Lett. 2012, 14, 4910) by Michio Kurosu at the University of Tennessee Health Science Center using the reagent 11, such as in the conversion of alcohol 10 to produce 12 in high yield. Hosahudya N. Gopi discovered (Chem. Commun. 2012, 48, 7085) that the conversion of thioacid 13 to amide 14 was rapidly promoted by CuSO4. A ruthenium-catalyzed dehydrative amidation procedure using azides and alcohols, such as the reaction of 15 with phenylethanol to produce 16, was reported (Org. Lett. 2012, 14, 6028) by Soon Hyeok Hong at Seoul National University. An alternative oxidative amidation was developed (Tetrahedron Lett. 2012, 53, 6479) by Chengjian Zhu at Nanjing University and the Shanghai Institute of Organic Chemistry who utilized catalytic tetrabutylammonium iodide and disubstituted formamides to convert alcohols such as 17 to amides 18. A redox catalysis strategy was developed (Angew. Chem. Int. Ed. 2012, 51, 12036) by Brandon L. Ashfeld at Notre Dame for the triphenylphosphine-catalyzed Staudinger ligation of carboxylic acid 19 to furnish amide 20. For direct catalytic amidation of carboxylic acids and amines such as in the conversion of 21 to 23, Dennis G. Hall at the University of Alberta reported (J. Org. Chem. 2012, 77, 8386) that the boronic acid 22 was a highly effective catalyst that operated at room temperature.

Development of a Visible Light Triggerable Traceless Staudinger Ligation Reagent

2018 ◽  
Vol 83 (21) ◽  
pp. 12998-13010 ◽  
Author(s):  
Peng Hu ◽  
Karsten Berning ◽  
Yun-Wah Lam ◽  
Isabel Hei-Ma Ng ◽  
Chi-Chung Yeung ◽  
...  
Keyword(s):  
Visible Light ◽  
Staudinger Ligation

Acidic and basic deprotection strategies of borane-protected phosphinothioesters for the traceless Staudinger ligation

2010 ◽  
Vol 18 (11) ◽  
pp. 3679-3686 ◽  
Author(s):  
Michaela Mühlberg ◽  
Da’san M.M. Jaradat ◽  
Rolf Kleineweischede ◽  
Ilona Papp ◽  
Decha Dechtrirat ◽  
...  
Keyword(s):  
Staudinger Ligation
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