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Relevant bibliographies by topics / Organic azide

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Academic literature on the topic 'Organic azide'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 April 2022

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Journal articles on the topic "Organic azide"

1

Vikulina, E. L., E. E. Romashin, D. I. Fedorov, I. K. Kukushkin, A. M. Pyzhov, and P. P. Purygin. "METHOD OF REGENERATION OF AZIDE ION." Vestnik of Samara University. Natural Science Series 20, no. 7 (2017): 163–67. http://dx.doi.org/10.18287/2541-7525-2014-20-7-163-167.

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In this article the results of research devoted to the development of methods of disposal and regeneration of azide ion contained in the liquid wastes are stated. As a rule, all existing methods of disposal of azide ion in the liquid wastes based on its destruction, which is not only economically impractical because it is irretrievably lost, but also dangerous, as this forms an extremely explosive and toxic hydrazoic acid, which signiﬁcantly increases the risk of the process of disposal of liquid wastes. Researches carried out by the authors allowed for the ﬁrst time to suggest an eﬀective met

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2

Tchertanov, Luba. "Structural metrics relationships in covalently bonded organic azides." Acta Crystallographica Section B Structural Science 55, no. 5 (1999): 807–9. http://dx.doi.org/10.1107/s0108768199003936.

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Geometrical parameters of covalently bonded organic azides have been analysed using X-ray structural data retrieved from the Cambridge Structural Database. The RNNN fragment geometry shows some important general features: (i) a preference for a trans C s configuration; (ii) bending of the N—N—N unit; (iii) substantially different N—N bond lengths in the azide group. Electron-density redistribution within the covalently bonded azide group (relative to that in the isolated azide anion) promotes the capacity of the terminal azide N atom to form hydrogen bonds.

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Monticelli, Serena, and Vittorio Pace. "Diethylaluminium Azide: A Versatile Reagent in Organic Synthesis." Australian Journal of Chemistry 68, no. 5 (2015): 703. http://dx.doi.org/10.1071/ch14712.

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The unique properties of diethylaluminium azide – arising from the Lewis acid aluminium and the nucleophilicity of the azide – make it a versatile reagent in organic synthesis. Ring-opening of epoxides, Michael-type additions, synthesis of acyl azides, and functionalizations of fullerene C60 will be discussed. Among the recently described uses of the reagent, particular attention will be devoted to the powerful Sedelmeier’s method to access 1H-tetrazol starting from nitriles.

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Schock, Marvin, and Stefan Bräse. "Reactive & Efficient: Organic Azides as Cross-Linkers in Material Sciences." Molecules 25, no. 4 (2020): 1009. http://dx.doi.org/10.3390/molecules25041009.

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The exceptional reactivity of the azide group makes organic azides a highly versatile family of compounds in chemistry and the material sciences. One of the most prominent reactions employing organic azides is the regioselective copper(I)-catalyzed Huisgen 1,3-dipolar cycloaddition with alkynes yielding 1,2,3-triazoles. Other named reactions include the Staudinger reduction, the aza-Wittig reaction, and the Curtius rearrangement. The popularity of organic azides in material sciences is mostly based on their propensity to release nitrogen by thermal activation or photolysis. On the one hand, th

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Israr, Muhammad, Changqing Ye, Munira Taj Muhammad, Yajun Li, and Hongli Bao. "Copper(I)-catalyzed tandem reaction: synthesis of 1,4-disubstituted 1,2,3-triazoles from alkyl diacyl peroxides, azidotrimethylsilane, and alkynes." Beilstein Journal of Organic Chemistry 14 (November 23, 2018): 2916–22. http://dx.doi.org/10.3762/bjoc.14.270.

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A copper-catalyzed azide–alkyne cycloaddition (CuAAC) reaction for the synthesis of 1,4-disubstituted 1,2,3-triazoles from alkyl diacyl peroxides, azidotrimethylsilane, and terminal alkynes is reported. The alkyl carboxylic acids is for the first time being used as the alkyl azide precursors in the form of alkyl diacyl peroxides. This method avoids the necessity to handle organic azides, as they are generated in situ, making this protocol operationally simple. The Cu(I) catalyst not only participates in the alkyl diacyl peroxides decomposition to afford alkyl azides but also catalyzes the subs

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6

Roux, Amélie, and Federico Cisnetti. "Click Variations on the Synthesis of 2-Nitrophenyl-4-aryl-1,2,3-triazoles without Isolation of 2-Nitrophenyl Azides." Synlett 31, no. 06 (2019): 610–14. http://dx.doi.org/10.1055/s-0039-1691524.

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We report a series of efficient procedures to prepare 2-nitrophenyl-4-aryl-1,2,3-triazoles avoiding the isolation of potentially hazardous 2-nitrophenyl azides. An organocatalyzed azide-enolate variant allows efficient access to the target compounds while it was shown that a metal-catalyzed azide-alkyne procedure involving a preliminary Sonogashira coupling was feasible starting from electron-deficient aryl iodides.

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Nasseri, Mohammad Ali, Seyyedeh Ameneh Alavi, Boshra Mahmoudi, and Milad Kazemnejadi. "A Facile Approach to Catalyst-Free Cyanation and Azidation of Organic Compounds and a One-Pot Preparation of 5-Substituted 1H-Tetrazoles by Using a Dimethyl Sulfoxide–Nitric Acid Combination." Synlett 30, no. 20 (2019): 2290–94. http://dx.doi.org/10.1055/s-0039-1690742.

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In this study, cyanations or azidations of imines were performed by using hydroxy(dimethyl)-λ4-sulfanecarbonitrile or azido(dimethyl)-λ4-sulfanol, respectively, prepared in situ by treatment of potassium cyanide or sodium azide with a dimethyl sulfoxide–nitric acid combination. Furthermore, a one-pot preparation of 5-substituted 1H-tetrazole derivatives was carried out by using this reagent combination in the presence of an aldehyde, hydroxylamine hydrochloride, and sodium azide under mild conditions.

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Kore, Nitin, and Pavel Pazdera. "New Stable Cu(I) Catalyst Supported on Weakly Acidic Polyacrylate Resin for “Click” Chemistry: Synthesis of 1,2,3-Triazole and Novel Synthesis of 1,2,3-Triazol-5-amine." Current Organic Synthesis 15, no. 4 (2018): 552–65. http://dx.doi.org/10.2174/1570179415666180110152642.

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Aim and Objective: The aim of our work is to demonstrate catalytic application of our previously reported simple Cu(I) ion supported on weakly acidic polyacrylate resin for Azide-Alkyne cycloaddition (CuAAC), Azide-Nitrile cycloaddition and in synthesis of 1-azido-4-methoxybenzene. Material and Method: To investigate the catalytic ability of title Cu(I) catalyst we performed the reaction of different aryl azide with a broader spectrum of different terminal alkyne and nitrile compounds. Results: The title supported Cu(I) catalyzes cycloaddition reactions of aryl azide with aliphatic, aromatic,

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9

Stamatatos, Theocharis C., and Eva Rentschler. "Organic chelate-free and azido-rich metal clusters and coordination polymers from the use of Me3SiN3: a new synthetic route to complexes with beautiful structures and diverse magnetic properties." Chemical Communications 55, no. 1 (2019): 11–26. http://dx.doi.org/10.1039/c8cc08854c.

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A new synthetic route to structurally novel and magnetically interesting 3d-metal azido clusters and coordination polymers is presented; the key reagent for the preparation of solely azido-bridged molecule-based species is the organic azide precursor Me<sub>3</sub>SiN<sub>3</sub>.

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Adronov, Alex, Kelvin Li, and Stuart McNelles. "Preparation and Properties of a Hydrolytically Stable Cyclooctyne-Containing Polymer." Synlett 29, no. 19 (2018): 2535–41. http://dx.doi.org/10.1055/s-0037-1610636.

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A poly[(phenylene vinylene)-co-dibenzocyclooctyne] polymer prepared by Wittig polymerization chemistry between dibenzocyclooctyne bisaldehyde [DIBO-(CHO)2] and bis(triethyleneglycol)phenylbis(tributylphosphonium) dibromide is reported. The resulting polymer exhibits moderate molecular weight (Mn: 10.5 kDa, Mw: 21.3 kDa, Ð: 2.02) and is fluorescent. It could be readily functionalized by strain-promoted alkyne-azide cycloadditon with different azides, and fluorescence of the polymer was preserved after functionalization. Grafting azide-terminated 5 kDa poly(ethylene glycol) monomethyl ether chai

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Dissertations / Theses on the topic "Organic azide"

1

Hartranft, Charles Alan. ""One-pot" synthesis of organic azides from alcohols and protected sugars /." Connect to resource online, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1229370336.

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Okumu, Antony A. "Development of a Safe and Efficient Alkyl Azide Synthesis using Arylsulfonyl Azide." Youngstown State University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1290962115.

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Kwarkoh, Angela. "Conversion of Alcohols to Alkyl Azides Using O-Nitrobenzenesulfonyl Azide." Youngstown State University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1380022166.

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Dobosh, Brian Joseph. "The Synthesis of Azides from Alcohols using Sulfonyl Azides." Youngstown State University / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219459733.

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Copeland, Christopher N. II. "Modified Conditions for Acyl Azide and Carbamate Synthesis." Youngstown State University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1473765784542178.

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Banerjee, Upasana. "Mechanistic Investigations into the Photoreactivity of Organic Azides in Solution, Crystals and Cryogenic Matrices." University of Cincinnati / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1623250627543686.

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Curry, Omadee S. "Reaction of o-Nitrobenzenesulfonyl Azide/n-Butyl Lithium with Hindered Alcohols." Youngstown State University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1379945812.

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Zhang, Jianjun. "Library Synthesis of Anticancer and Antibacterial Agents via Azide Chemistry." DigitalCommons@USU, 2010. https://digitalcommons.usu.edu/etd/711.

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Various anticancer and antibacterial agents have been synthesized via azide chemistry by taking advantage of carbohydrate. Starting from the synthesis of 14 glycosyl azides, a library of carbohydrate-oxazolidinone conjugates and a library of carbohydrate-cyclopamine conjugates with biological interests were synthesized based on a highly efficient "click reaction" assisted by sonication. Some of the conjugates have improved solubility and enhanced anticancer activity. A library of neomycin B derivatives with various modifications at the 5" position has been synthesized. Two leads exhibit

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9

Gatlin, DeVonna M. M. S. "Characterization and Photodynamics of Reactive Intermediates for Various Carbonyl-Based Systems: Alkyl Azides, Vinyl Azides, and Beta-Ketoester Moieties." University of Cincinnati / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1535380770508755.

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Mandel, Sarah Marie. "Photolysis of Alkyl Azides Containing an Aryl Ketone Chromophore in Solution and the Solid-state." University of Cincinnati / OhioLINK, 2004. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1099539420.

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Books on the topic "Organic azide"

1

Brse, Stefan, and Klaus Banert, eds. Organic Azides. John Wiley & Sons, Ltd, 2009. http://dx.doi.org/10.1002/9780470682517.

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2

Bräse, Stefan. Organic azides: Syntheses and applications. John Wiley, 2010.

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3

Haines, Alan H. Methods for the oxidation of organic compounds: Alcohols, alcohol derivatives, alkyl halides, nitroalkanes, alkyl azides, carbonyl compounds, hydroxyarenes and aminoarenes. Academic, 1988.

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4

Stefan, Bräse, and Banert Klaus, eds. Organic azides: Syntheses and applications. Wiley, 2009.

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Organic azides: Syntheses and applications. Wiley, 2009.

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Book chapters on the topic "Organic azide"

1

Gillaizeau, Isabelle, and Nicolas Gigant. "Alkyl and Acyl Azide Rearrangements." In Molecular Rearrangements in Organic Synthesis. John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118939901.ch4.

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Mandal, Joydeb, and S. Ramakrishnan. "Azide-Alkyne Click Reaction in Polymer Science." In Click Reactions in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527694174.ch7.

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Hoogstede, Freek A. B. M., and Floris P. J. T. Rutjes. "Applications of the Cu-Catalyzed Azide-Alkyne Cycloaddition (CuAAC) in Peptides." In Click Reactions in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527694174.ch5.

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4

Amblard, Franck, Ozkan Sari, Sebastien Boucle, Ahmed Khalil, and Raymond F. Schinazi. "Modifications of Nucleosides, Nucleotides, and Nucleic Acids using Huisgen's [3+2] Azide-Alkyne Cycloaddition: Opening Pandora's Box." In Click Reactions in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527694174.ch10.

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5

Ricardo, Carolynne L., and Tomislav Pintauer. "Highly Efficient Organic and Macromolecular Synthesis Using Sequential Copper Catalyzed Azide-Alkyne [3+2] Cycloaddition and ATRA/ATRP." In ACS Symposium Series. American Chemical Society, 2012. http://dx.doi.org/10.1021/bk-2012-1100.ch006.

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6

Lane, J. D., C. J. Pickett, and D. R. Stanley. "By Adding Organic Azides." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145227.ch62.

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7

Zhang, Bo, and Ning Jiao. "Nitrogenation Strategy for the Synthesis of Organic Azides." In Nitrogenation Strategy for the Synthesis of N-containing Compounds. Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-10-2813-7_6.

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Dommerholt, Jan, Floris P. J. T. Rutjes, and Floris L. van Delft. "Strain-Promoted 1,3-Dipolar Cycloaddition of Cycloalkynes and Organic Azides." In Cycloadditions in Bioorthogonal Chemistry. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-29686-9_4.

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9

Molteni, G. "Azide Cycloadditions." In Water in Organic Synthesis. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-206-00318.

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Ogawa, C., and S. Kobayashi. "Epoxide Ring Opening with Azide." In Water in Organic Synthesis. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-206-00435.

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Conference papers on the topic "Organic azide"

1

Godoy Prieto, Leonela, Alicia Chopa, and Maria Lockhart. "Tributylstannyl Azide as Efficient Reagent in the Synthesis of Aryl Azides from Aryl Amines." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a049.

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Gomes, Amenson T., and Silvio Cunha. "Synthesis of Acyclic -Enaminones Through Reaction of Enones and Benzyl Azide." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0333-1.

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Lavilla, Rodolfo, Nicolas Isambert, Federica Catti, Mª-José Arévalo, and Ricardo Salazar. "Tandem Azide Conjugate Addition –Click Chemistry : Scope and Limitations." In The 11th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01316.

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4

Canduzini*(PG), Hugo A., Eliane C. Pedrozo, Flávia G. Manarin, and Hélio A. Stefani. "Synthesis and functionalization of 1,2,3-triazoles via cycloaddition [3 +2] azide in the presence of acetylenes." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0350-1.

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Gámez-Montaño, Rocío, Manuel A. Rentería-Gómez, and Alejandro Islas-Jácome. "Synthesis of 1-tetrazolyl-1,2,3,4-tetrahydroisoquinoline bound-type bis-heterocycles via oxidative Ugi-azide reaction." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a030.

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Gámez-Montaño, Rocío, Alicia E. Cruz-Jiménez, and Angel Rentería-Gómez. "Synthesis of 1,5-disubstituted-1H-tetrazole methane-linked bis-heterocycles via Ugi-azide." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a029.

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Dinh Thanh, Nguyen, Le The Duan, Nguyen Thi Minh Nguyet, Le Thi Hoai, and Nguyen Thi Thu Ha. "STUDY ON REACTION OF SUBSTITUTED 4-METHYLQUINOLIN-2(1H)-ONES WITH SODIUM AZIDE." In The 21st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04771.

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8

Gámez-Montaño, Rocío, Nancy V. Alvarez-Rodríguez, and Alejandro Islas-Jácome. "Synthesis of 2-tetrazolylmethyl-tetrahydro-1H-beta-carboline methane-linked bis-heterocycles via one pot Ugi-azide / Pictet-Spengler process." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a028.

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LAW, C., A. LEE, and A. RANDOLPH. "Droplet combustion of organic azides." In 21st Joint Propulsion Conference. American Institute of Aeronautics and Astronautics, 1985. http://dx.doi.org/10.2514/6.1985-1108.

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Dutra, Luiz Gustavo, and Marcus Mandolesi Sá. "Milder Preparation of a g-Azido-a-diazo-b-keto Ester by Consecutive Introduction of Azido and Diazo Groups." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0182-2.

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