References
[1] F. Fleming, Nitrile-containing natural products, Nat. Prod. Rep., 16 (1999) 597-606.
[2] F.F. Fleming, L. Yao, P. Ravikumar, L. Funk, B.C. Shook, Nitrile-containing pharmaceuticals: efficacious roles of the nitrile pharmacophore, J. Med. Chem., 53 (2010) 7902-7917.
[3] M. Katono, T. Bessho, S. Meng, R. Humphry-Baker, G. Rothenberger, S.M. Zakeeruddin, E. Kaxiras, M. Grätzel, D-π-A dye system containing cyano-benzoic acid as anchoring group for dye-sensitized solar cells, Langmuir, 27 (2011) 14248-14252.
[4] C. Astbury, L.K. Conway, C. Gillespie, K. Hodge, E. Innes, A.R. Kennedy, A structural study of seven salt forms of sulfonated azo dyes containing nitrile functional groups, Dyes Pigm., 97 (2013) 100-104.
[5] U. Dutta, D.W. Lupton, D. Maiti, Aryl nitriles from alkynes using tert-butyl nitrite: Metal-free approach to C-C bond cleavage, Org. Lett., 18 (2016) 860-863.
[6] J. Wang, F. Xu, T. Cai, Q. Shen, Addition of amines to nitriles catalyzed by ytterbium amides: An efficient one-step synthesis of monosubstituted N-arylamidines, Org. Lett., 10 (2008) 445-448.
[7] T. Horneff, S. Chuprakov, N. Chernyak, V. Gevorgyan, V.V. Fokin, Rhodium-catalyzed transannulation of 1, 2, 3-triazoles with nitriles, J. Am. Chem. Soc., 130 (2008) 14972-14974.
[8] S. Lu, J. Wang, X. Cao, X. Li, H. Gu, Selective synthesis of secondary amines from nitriles using Pt nanowires as a catalyst, Chem. Commun., 50 (2014) 3512-3515.
[9] X. Wang, Y. Huang, Y. Xu, X. Tang, W. Wu, H. Jiang, Palladium-catalyzed denitrogenative synthesis of aryl ketones from arylhydrazines and nitriles using O2 as sole oxidant, J. Org. Chem., 82 (2017) 2211-2218.
[10] G. Yan, Y. Zhang, J. Wang, Recent advances in the synthesis of aryl nitrile compounds, Adv. Synth. Catal., 359 (2017) 4068-4105.
[12a] E. Vessally, H. Saeidian, A. Hosseinian, L. Edjlali, A. Bekhradnia, A review on synthetic applications of oxime esters, Curr.Org. Chem., 21 (2017) 249-271;
[12b] E. Vessally, L. Edjlali, A. Hosseinian, A. Bekhradnia, M.D. Esrafili, Novel routes to quinoline derivatives from N-propargylamines, RSC Adv., 6 (2016) 49730-49746;
[12c] E. Vessally, A. Hosseinian, L. Edjlali, A. Bekhradnia, M.D. Esrafili, New page to access pyridine derivatives: synthesis from N-propargylamines, RSC Adv., 6 (2016) 71662-71675;
[12d] E. Vessally, A. Hosseinian, L. Edjlali, A. Bekhradnia, M. D Esrafili, New page to access pyrazines and their ring fused analogues: Synthesis from N-propargylamines, Curr.Org. Synth., 14 (2017) 557-567;
[12e] E. Vessally, A. Hosseinian, L. Edjlali, A. Bekhradnia, M.D. Esrafili, New route to 1, 4-oxazepane and 1, 4-diazepane derivatives: synthesis from N-propargylamines, RSC Adv., 6 (2016) 99781-99793;
[12f] E. Vessally, S. Soleimani-Amiri, A. Hosseinian, L. Edjlali, A. Bekhradnia, New protocols to access imidazoles and their ring fused analogues: synthesis from N-propargylamines, RSC Adv., 7 (2017) 7079-7091;
[12g] M. Babazadeh, S. Soleimani-Amiri, E. Vessally, A. Hosseinian, L. Edjlali, Transition metal-catalyzed [2+ 2+ 2] cycloaddition of nitrogen-linked 1, 6-diynes: a straightforward route to fused pyrrolidine systems, RSC Adv., 7 (2017) 43716-43736;
[12h] E. Vessally, A. Hosseinian, L. Edjlali, E. Ghorbani-Kalhor, R. Hosseinzadeh-Khanmiri, Intramolecular cyclization of N-propargyl anilines: a new synthetic entry into highly substituted indoles, J. Iran. Chem. Soc., 14 (2017) 2339-2353;
[12i] E. Vessally, A. Hosseinian, L. Edjlali, M. Babazadeh, R. Hosseinzadeh-Khanmiri, New strategy for the synthesis of morpholine cores: synthesis from N-propargylamines, Iran. J. Chem. Chem. Eng., 36 (2017) 1-13;
[12j] S. Arshadi, E. Vessally, M. Sobati, A. Hosseinian, A. Bekhradnia, Chemical fixation of CO2 to N-propargylamines: a straightforward route to 2-oxazolidinones, J. CO2 Util., 19 (2017) 120-129;
[12k] E. Vessally, M. Babazadeh, K. Didehban, A. Hosseinian, L. Edjlali, Intramolecular ipso-Cyclization of N-Arylpropiolamides: A Novel and Straightforward Synthetic Approach for Azaspiro [4.5] decatrien-2-ones, Curr. Org. Chem., 22 (2018) 286-297;
[12l] E. Vessally, M. Babazadeh, K. Didehban, A. Hosseinian, L. Edjlali, Intramolecular Cyclization of N-Arylpropiolamides: A New Strategy for the Synthesis of Functionalized 2-Quinolones, Curr. Org. Chem., 21 (2017) 2561-2572.
[13a] S. Soleimani-Amiri, E. Vessally, M. Babazadeh, A. Hosseinian, L. Edjlali, Intramolecular cyclization of N-allyl propiolamides: a facile synthetic route to highly substituted γ-lactams (a review), RSC Adv., 7 (2017) 28407-28418;
[13b] E. Vessally, M. Babazadeh, A. Hosseinian, L. Edjlali, L. Sreerama, Recent Advances in Synthesis of Functionalized β-Lactams through Cyclization of N-Propargyl Amine/Amide Derivatives, Curr. Org. Chem., 22 (2018) 199-205;
[13c] E. Vessally, A. Hosseinian, M. Babazadeh, L. Edjlali, R. Hosseinzadeh-Khanmiri, Metal Catalyzed Carboxylative Coupling of Terminal Alkynes, Organohalides and Carbon Dioxide: A Novel and Promising Synthetic Strategy toward 2-Alkynoates (A Review), Curr. Org. Chem., 22 (2018) 315-322;
[13d] S. Arshadi, E. Vessally, A. Hosseinian, S. Soleimani-amiri, L. Edjlali, Three-component coupling of CO2, propargyl alcohols, and amines: An environmentally benign access to cyclic and acyclic carbamates (A Review), J. CO2 Util., 21 (2017) 108-118;
[13e] E. Vessally, S. Soleimani-Amiri, A. Hosseinian, L. Edjlali, M. Babazadeh, Chemical fixation of CO2 to 2-aminobenzonitriles: a straightforward route to quinazoline-2, 4 (1H, 3H)-diones with green and sustainable chemistry perspectives, J. CO2 Util., 21 (2017) 342-352;
[13f] E. Vessally, M. Babazadeh, A. Hosseinian, S. Arshadi, L. Edjlali, Nanocatalysts for chemical transformation of carbon dioxide, J. CO2 Util., 21 (2017) 491-502;
[13g] E. Vessally, K. Didehban, M. Babazadeh, A. Hosseinian, L. Edjlali, Chemical fixation of CO2 with aniline derivatives: A new avenue to the synthesis of functionalized azole compounds (A review), J. CO2 Util., 21 (2017) 480-490;
[13h] E. Vessally, A. Hosseinian, L. Edjlali, M. Babazadeh, K. Didehban, Chemical Fixation of CO2 to Allylic (α-Allenylic) Amines: A Green Route to Synthesis of Functionalized 2-Oxazolidones, Mini-Rev. Org. Chem., 15 (2018) 315-323;
[13i] A. Hosseinian, M. Babazadeh, L. Edjlali, Z. Rahmani, E. Vessally, Intramolecular Cyclization of Aryl Propargyl Ethers: A Straightforward and Convenient Approach to Benzofuran Derivatives, Curr. Org. Synth., 15 (2018) 972-981;
[13j] E. Vessally, R. Mohammadi, A. Hosseinian, L. Edjlali, M. Babazadeh, Three component coupling of amines, alkyl halides and carbon dioxide: An environmentally benign access to carbamate esters (urethanes), J. CO2 Util., 24 (2018) 361-368;
[13k] E. Vessally, K. Didehban, R. Mohammadi, A. Hosseinian, M. Babazadeh, Recent advantages in the metal (bulk and nano)-catalyzed S-arylation reactions of thiols with aryl halides in water: a perfect synergy for eco-compatible preparation of aromatic thioethers, J. Sulfur Chem., 39 (2018) 332-349;
[13l] K. Didehban, E. Vessally, A. Hosseinian, L. Edjlali, E.S. Khosroshahi, Nanocatalysts for C–Se cross-coupling reactions, RSC Adv., 8 (2018) 291-301;
[14a] A. Hosseinian, S. Farshbaf, L.Z. Fekri, M. Nikpassand, E. Vessally, Cross-Dehydrogenative Coupling Reactions Between P (O)–H and X–H (X= S, N, O, P) Bonds, Top. Curr. Chem., 376 (2018) 23;
[14b] F.A.H. Nasab, L.Z. Fekri, A. Monfared, A. Hosseinian, E. Vessally, Recent advances in sulfur–nitrogen bond formation via cross-dehydrogenative coupling reactions, RSC Adv., 8 (2018) 18456-18469;
[14c] A. Hosseinian, S. Ahmadi, A. Monfared, P.D. Nezhad, E. Vessally, Nano-structured Catalytic Systems in Cyanation of Aryl Halides with K4 [Fe (CN) 4], Curr. Org. Chem., 22 (2018) 1862-1874;
[14d] A. Hosseinian, L. Zare Fekri, A. Monfared, E. Vessally, M. Nikpassand, Transition-metal-catalyzed C–N cross-coupling reactions of N-unsubstituted sulfoximines: a review, J. Sulfur Chem., 39 (2018) 674-698;
[14e] A. Hosseinian, S. Ahmadi, F.A.H. Nasab, R. Mohammadi, E. Vessally, Cross-Dehydrogenative C–H/S–H Coupling Reactions, Top. Curr. Chem., 376 (2018) 39;
[14f] A. Hosseinian, F.A.H. Nasab, S. Ahmadi, Z. Rahmani, E. Vessally, Decarboxylative cross-coupling reactions for P (O)–C bond formation, RSC Adv., 8 (2018) 26383-26398.
[15] A. Hosseinian, M. Babazadeh, L. Edjlali, Z. Rahmani, E. Vessally, Intramolecular cyclization of aryl propargyl ethers: A straightforward and convenient approach to benzofuran derivatives DOI: 0.2174/1570179415666180829120105.
[16] V.K. Das, S. Harsh, N. Karak, Highly efficient and active silver nanoparticle catalyzed conversion of aldehydes into nitriles: a greener, convenient, and versatile ‘NOSE’approach, Tetrahedron Lett., 57 (2016) 549-553.
[17] M. Nasrollahzadeh, M. Atarod, S.M. Sajadi, Biosynthesis, characterization and catalytic activity of Cu/RGO/Fe3O4 for direct cyanation of aldehydes with K4[Fe(CN)6], J. Colloid Interface Sci. 486 (2017) 153-162.
[18] M. Nasrollahzadeh, S.S. Momeni, S.M. Sajadi, Green synthesis of copper nanoparticles using Plantago asiatica leaf extract and their application for the cyanation of aldehydes using K4[Fe(CN)6], J. Colloid Interface Sci., 506 (2017) 471-477.
[19] F. Verma, P. Shukla, S.R. Bhardiya, M. Singh, A. Rai, V.K. Rai, Visible light-induced direct conversion of aldehydes into nitriles in aqueous medium using Co@g-C3N4 as photocatalyst, Catal. Commun., 119 (2018) 76-81.
[20] P. Ghosh, B. Saha, G.C. Pariyar, A. Tamang, R. Subba, Fe3O4-nanoparticles catalyzed an efficient synthesis of nitriles from aldehydes, Tetrahedron Lett., 57 (2016) 3618-3621.
[21] K. Murugesan, T. Senthamarai, M. Sohail, M. Sharif, N.V. Kalevaru, R.V. Jagadeesh, Stable and reusable nanoscale Fe2O3-catalyzed aerobic oxidation process for the selective synthesis of nitriles and primary amides, Green Chem., 20 (2018) 266-273.
[22] R.V. Jagadeesh, H. Junge, M. Beller, Green synthesis of nitriles using non-noble metal oxides-based nanocatalysts, Nat. Commun., 5 (2014) 4123.
[23] S. Shang, L. Wang, W. Dai, B. Chen, Y. Lv, S. Gao, High catalytic activity of mesoporous Co–N/C catalysts for aerobic oxidative synthesis of nitriles, Catal. Sci. Technol., 6 (2016) 5746-5753.
[24] F. Mao, Z. Qi, H. Fan, D. Sui, R. Chen, J. Huang, Heterogeneous cobalt catalysts for selective oxygenation of alcohols to aldehydes, esters and nitriles, RSC Adv., 7 (2017) 1498-1503.
[25] F. Ziaee, M. Gholizadeh, S.M. Seyedi, Magnetically recoverable lanthanum hydroxide as an efficient catalyst for Aerobic Oxidative Conversions of primary alcohols to the nitriles, Appl. Organomet. Chem., 32 (2018) e4253.
[26] Y. Preger, T.W. Root, S.S. Stahl, Platinum-based heterogeneous catalysts for nitrile synthesis via aerobic oxidative coupling of alcohols and ammonia, ACS Omega, 3 (2018) 6091-6096.
[27] R.V. Jagadeesh, H. Junge, M. Beller, “Nanorust” catalyzed benign oxidation of amines for selective synthesis of nitriles, ChemSusChem, 8 (2015) 92-96.
[28] K. Natte, R.V. Jagadeesh, M. Sharif, H. Neumann, M. Beller, Synthesis of nitriles from amines using nanoscale Co3O4-based catalysts via sustainable aerobic oxidation, Org. Biomol. Chem., 14 (2016) 3356-3359
)
)