Results 241 to 250 of about 227,214 (300)

Azides

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Chin‐Kang Sha, A. K. Mohanakrishnan
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Dual Roles of Azide: Dearomative Dimerization of Furfuryl Azides

The Journal of Organic Chemistry, 2022
A dearomative dimerization of furfuryl azides for the construction of furfuryl triazoles is developed. As a rare leaving group, azide is capable of initiating the generation of a furfuryl cation under the Lewis acid-catalyzed conditions, followed by reacting with the other azide to realize an intermolecular [3 + 2] cycloaddition/furan ring-opening ...
Zhe Hao, Penggang Zhao, Qingzhao Xing, Abdul Wahab, Ziwei Gao, Jing Gou, Binxun Yu   +6 more
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Liquid Azide Salts

Inorganic Chemistry, 2008
Ionic liquid azides from azidoethyl, alkyl, and alkenyl substituted derivatives of 1,2,4- and 1,2,3-amino-triazoles were prepared and examined for the first time to investigate their structural and physical properties. All reported salts possess melting points below 100 degrees C.
Stefan, Schneider, Tommy, Hawkins, Michael, Rosander, Jeffrey, Mills, Adam, Brand, Leslie, Hudgens, Greg, Warmoth, Ashwani, Vij   +7 more
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Ab initio Study of Energetic Solids: Cupric Azide, Mercuric Azide, and Lead Azide

ChemInform, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Weihua, Zhu, Heming, Xiao
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Pyrolysis of aryl azides. II. Naphthyl azides

Australian Journal of Chemistry, 1972
Kinetic studies of the pyrolyses of 1- and 2-naphthyl azides reveal neighbouring group participation by nitro and phenylazo substituents. The acceleration observed in 1-nitro-2-naphthyl azide, 1-phenylazo-2-naphthyl azide, and 2-nitro-1-naphthyl azide is 1730-, 211-, and 23.6-fold, respectively, in nitrobenzene solution at 120º.
G Boshev, LK Dyall, PR Sadler
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Binary Zinc Azides

Chemistry – A European Journal, 2016
AbstractPure, solvent‐free Zn(N3)2 was prepared by reaction of diethyl zinc and hydrazoic acid in aprotic solvents. The single‐crystal structure determination, along with the comprehensive characterization of α‐Zn(N3)2 and two metastable polymorphs, could be achieved for the first time.
Axel, Schulz, Alexander, Villinger
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Kinetic Study of the Radical Azidation with Sulfonyl Azides*

Australian Journal of Chemistry, 2013
Rate constants for the reaction between a secondary alkyl radical and two different sulfonyl azides were determined using bimolecular competing radical reactions. The rates of azidation were determined by competition with hydrogen atom transfer from tris(trimethylsilyl)silane ((TMS)3SiH) of the 4-phenylcyclohexyl radical.
Weidner Karin, Renaud Philippe
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Azide Phosphoramidite in Direct Synthesis of Azide-Modified Oligonucleotides

Organic Letters, 2014
Azide and phosphoramidite functions were found to be compatible within one molecule and stable for months in solution kept frozen at -20 °C. An azide-carrying phosphoramidite was used for direct introduction of multiple azide modifications into synthetic oligonucleotides.
Maksim A, Fomich, Maksim V, Kvach, Maksim J, Navakouski, Christoph, Weise, Alexander V, Baranovsky, Vladimir A, Korshun, Vadim V, Shmanai   +6 more
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Azide

Mutation Research/Reviews in Genetic Toxicology, 1978
A, Kleinhofs, W M, Owais, R A, Nilan
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Alkinphosphonite für sequenzielle Azid‐Azid‐Kupplungen

Angewandte Chemie, 2013
M. Robert J. Vallée, Lukas M. Artner, Jens Dernedde, Christian P. R. Hackenberger   +3 more
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