Staudinger reaction

Definition: A joining of an organic azide and a tertiary phosphine to give a phosphazo compound.

ID: RXNO:0000066


More about the RSC Name Reaction Ontology (RXNO)

Articles referencing this term

Component exchange as a synthetically advantageous strategy for the preparation of bicyclic cage compounds
Mateo Alajarín, José Berná, Carmen López-Leonardo and Jonathan W. Steed, Chem. Commun., 2008 , 2337
DOI: 10.1039/b801299g

Tracking reactive intermediates in phosphine-promoted reactions with ambiphilic phosphino-boranes
Sylvie Moebs-Sanchez, Ghenwa Bouhadir, Nathalie Saffon, Laurent Maron and Didier Bourissou, Chem. Commun., 2008 , 3435
DOI: 10.1039/b805161e

Carbohydrate microarrays as powerful tools in studies of carbohydrate-mediated biological processes
Sungjin Park, Myung-Ryul Lee and Injae Shin, Chem. Commun., 2008 , 4389
DOI: 10.1039/b806699j

Chemoenzymatic synthesis of GDP-azidodeoxymannoses: non-radioactive probes for mannosyltransferase activity
Silvia Marchesan and Derek Macmillan, Chem. Commun., 2008 , 4321
DOI: 10.1039/b807016d

Computational and experimental tools in solving some mechanistic problems in the chemistry of Fischer carbene complexes
Miguel A. Sierra, Israel Fernández and Fernando P. Cossío, Chem. Commun., 2008 , 4671
DOI: 10.1039/b807806h

1-Azadienes in cycloaddition and multicomponent reactions towards N-heterocycles
Bas Groenendaal, Eelco Ruijter and Romano V. A. Orru, Chem. Commun., 2008 , 5474
DOI: 10.1039/b809206k

Novel strategies for the site-specific covalent labelling of nucleic acids
Samuel H. Weisbrod and Andreas Marx, Chem. Commun., 2008 , 5675
DOI: 10.1039/b809528k

Internal amide-triggered cycloaromatization of maduropeptin-like nine-membered enediyne
Yutaro Norizuki, Kazuo Komano, Itaru Sato and Masahiro Hirama, Chem. Commun., 2008 , 5372
DOI: 10.1039/b811355f

Enantiopure imidazolinium-dithiocarboxylates as highly selective novel organocatalysts
Oksana Sereda, Amélie Blanrue and René Wilhelm, Chem. Commun., 2009 , 1040
DOI: 10.1039/b817991c

Towards quorum-quenching catalytic antibodies
Prashant B. Kapadnis, Evan Hall, Madeleine Ramstedt, Warren R. J. D. Galloway, Martin Welch and David R. Spring, Chem. Commun., 2009 , 538
DOI: 10.1039/b819819e

A fluorogenic dye activated by S-nitrosothiols
Jia Pan, Jonathan A. Downing, Jeanne L. McHale and Ming Xian, Mol. BioSyst., 2009 , 5 , 918
DOI: 10.1039/b822283e

Chemically-selective surface glyco-functionalization of liposomes through Staudinger ligation
Hailong Zhang, Yong Ma and Xue-Long Sun, Chem. Commun., 2009 , 3032
DOI: 10.1039/b822420j

Aza-Wittig access to chiral imidazol(in)es
Patrick Loos, Matthias Riedrich and Hans-Dieter Arndt, Chem. Commun., 2009 , 1900
DOI: 10.1039/b822436f

Metabolic profiling of Helicobacter pylori glycosylation
Maria B. Koenigs, Elizabeth A. Richardson and Danielle H. Dube, Mol. BioSyst., 2009 , 5 , 909
DOI: 10.1039/b902178g

Prenyltransferase substrate binding pocket flexibility and its application in isoprenoid profiling
Youli Xiao, Miranda Machacek, Kent Lee, Tomohisha Kuzuyama and Pinghua Liu, Mol. BioSyst., 2009 , 5 , 913
DOI: 10.1039/b902370d

DNA templated nucleophilic aromatic substitution reactions for fluorogenic sensing of oligonucleotides
Aya Shibata, Hiroshi Abe, Mika Ito, Yuko Kondo, Shigeru Shimizu, Kyoko Aikawa and Yoshihiro Ito, Chem. Commun., 2009 , 6586
DOI: 10.1039/b912896d

Synthesis and antibacterial activity evaluation of C-5 side chain modified analogues of FYL-66, a potential agent against methicillin-resistant Staphylococcus aureus
Xiaoyan Yang, Zicheng Li, Zhenling Wang, Zitai Sang, Haiyue Long, Jianying Tang, Tao Yang, Yuanyuan Liu and Youfu Luo, Med. Chem. Commun., 2015 , 6 , 1156
DOI: 10.1039/c5md00101c