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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 40, 2010 - Issue 5
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Original Articles

N-Nitrosation of Secondary Amines Using p-TSA-NaNO2 as a Novel Nitrosating Agent Under Mild Conditions

Sanjay P. Borikar Division of Organic Chemistry, National Chemical Laboratory, Pune, India
&
Vincent Paul Division of Organic Chemistry, National Chemical Laboratory, Pune, IndiaCorrespondence[email protected]
Pages 654-660 | Received 05 Feb 2009, Published online: 04 Feb 2010

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Pinki Gaur & Shaibal Banerjee. (2019) Oxone-sodium nitrite mediated N-nitrosamines formation under mild conditions from secondary amines. Synthetic Communications 49:17, pages 2270-2279.
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Articles from other publishers (23)

Rojan Ali, Rasool Babaahmadi, Matthew Didsbury, Rebecca Stephens, Rebecca L. Melen & Thomas Wirth. (2023) Flow Electrochemistry for the N ‐Nitrosation of Secondary Amines . Chemistry – A European Journal 29:32.
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Wisut Wichitnithad, Siriwan Nantaphol, Kachathong Noppakhunsomboon & Pornchai Rojsitthisak. (2023) An update on the current status and prospects of nitrosation pathways and possible root causes of nitrosamine formation in various pharmaceuticals. Saudi Pharmaceutical Journal 31:2, pages 295-311.
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Volker Derdau & Martin Sandvoss. (2023) Synthesis and analysis of isotopically stable labeled nitrosamines as mass spectrometry standards for drug impurity quality control. Journal of Labelled Compounds and Radiopharmaceuticals 66:2, pages 41-46.
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Karu Ramesh, Hun Young Kim & Kyungsoo Oh. (2023) Catalytic Aerobic N-Nitrosation by Secondary Nitroalkanes in Water: A Tandem Diazotization of Aryl Amines and Azo Coupling. Organic Letters 25:2, pages 449-453.
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Kyungsoo Oh. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis 1 5 .
S. Yu. Panshina, A. A. Bakibaev, A. A. Borodaenko & V. S. Malkov. (2021) N-Nitrosation of Glycolurils Catalyzed by 1-Hydroxyethylidene-1,1-diphosphonic Acid. Russian Journal of Organic Chemistry 57:11, pages 1847-1852.
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Shaun W. P. Rees, Tayla A. Rees, Euphemia Leung, Christopher S. Walker, David Barker & Lisa I. Pilkington. (2021) Incorporation of a Nitric Oxide Donating Motif into Novel PC-PLC Inhibitors Provides Enhanced Anti-Proliferative Activity. International Journal of Molecular Sciences 22:21, pages 11518.
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Ying Wang, Shiqi You, Mengyao Ruan, Feiyi Wang, Chao Ma, Cuifen Lu, Guichun Yang, Zuxing Chen & Meng Gao. (2021) The Use of Potassium/Sodium Nitrite as a Nitrosating Agent in the Electrooxidative N ‐Nitrosation of Secondary Amines . European Journal of Organic Chemistry 2021:22, pages 3289-3293.
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Jordan D. Galloway, Cristian Sarabia, James C. Fettinger, Hrant P. Hratchian & Ryan D. Baxter. (2021) Versatile New Reagent for Nitrosation under Mild Conditions. Organic Letters 23:9, pages 3253-3258.
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Saroj Ranjan De. (2021) N ‐Nitroso As A Novel Directing Group in Transition‐Metal‐Catalyzed C( sp 2 )−H Bond Functionalizations of N ‐Nitrosoanilines . Asian Journal of Organic Chemistry 10:5, pages 980-1011.
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Pei‐Long Wang, Yan Wang, Yan Li & Xi‐Sheng Wang. (2020) Rh(III)‐Catalyzed N‐Nitroso Directed C‐H Arylation for Facile Construction of Diverse N‐Hetero Biaryl Compounds. Chemistry – An Asian Journal 15:22, pages 3825-3828.
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Rocío López-RodríguezJames A. McManusNatasha S. MurphyMartin A. OttMichael J. Burns. (2020) Pathways for N -Nitroso Compound Formation: Secondary Amines and Beyond . Organic Process Research & Development 24:9, pages 1558-1585.
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Wei-Hsuan Wu, Paul Thomas, Paul Hume & Jianyong Jin. (2018) Effective Conversion of Amide to Carboxylic Acid on Polymers of Intrinsic Microporosity (PIM-1) with Nitrous Acid. Membranes 8:2, pages 20.
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Xiao-Feng Wu WuXinxin Qi, Jin-Bao Peng & Xiao-Feng Wu. 2017. Solvents as Reagents in Organic Synthesis. Solvents as Reagents in Organic Synthesis 377 402 .
Norio Sakai, Minoru Sasaki & Yohei Ogiwara. (2015) Copper( ii )-catalyzed oxidative N -nitrosation of secondary and tertiary amines with nitromethane under an oxygen atmosphere . Chemical Communications 51:58, pages 11638-11641.
Crossref
Carles Miró Sabaté & Henri Delalu. (2015) Synthesis and Characterization of Secondary Nitrosamines from Secondary Amines Using Sodium Nitrite and p ‐Toluenesulfonic Acid . Chemistry – An Asian Journal 10:3, pages 674-678.
Crossref
Dan-Dan Li, Yi-Xuan Cao & Guan-Wu Wang. (2015) Palladium-catalyzed ortho-acyloxylation of N-nitrosoanilines via direct sp 2 C–H bond activation . Organic & Biomolecular Chemistry 13:25, pages 6958-6964.
Crossref
Jie Zhang, Jiewen Jiang, Yuling Li & Xiaobing Wan. (2013) Iodide-Catalyzed Synthesis of N -Nitrosamines via C–N Cleavage of Nitromethane . The Journal of Organic Chemistry 78:22, pages 11366-11372.
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Hamid Goudarziafshar, Arash Ghorbani‐Choghamarani & Laila Hadian. (2013) N ‐Nitrosation of Secondary Amines Using Supported Perchloric Acid on Silica Gel and Stereoselectivity Study of Nitrosated Products . Journal of the Chinese Chemical Society 60:10, pages 1272-1276.
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Satoshi Iwata, Masato Senoo, Takeshi Hata & Hirokazu Urabe. (2013) Synthesis of S -Aryl Arenethiosulfonates from N , N -Di(arenesulfonyl)hydrazines: Reduction of Sulfonyl Chlorides with an Organic Reagent . Heteroatom Chemistry 24:4, pages 336-344.
Crossref
Hima K. Potturi, Ras K. Gurung & Yuqing Hou. (2011) Nitromethane with IBX/TBAF as a Nitrosating Agent: Synthesis of Nitrosamines from Secondary or Tertiary Amines under Mild Conditions. The Journal of Organic Chemistry 77:1, pages 626-631.
Crossref
Patrizia Gentili & Silvia Pedetti. (2012) A remarkably simple α-oximation of aldehydes via organo-SOMO catalysis. Chemical Communications 48:43, pages 5358.
Crossref
Sanjay P. Borikar & Vincent Paul. (2010) ChemInform Abstract: N‐Nitrosation of Secondary Amines Using p‐TSA‐NaNO 2 as a Novel Nitrosating Agent under Mild Conditions. . ChemInform 41:30.
Crossref

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