Microwave-Accelerated Solvent-Free Synthesis of Thioketones, Thiolactones, Thioamides, Thionoesters, and Thioflavonoids

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1. Dharmesh J. Shah, Anuj S. Sharma, Vinay S. Sharma, Vinod Kumar Vishwakarma, Achalkumar Ammathnadu Sudhakar, Pranav S. Shrivastav, Rajender S. Varma. Microcrystalline Cellulose Decorated with Fe3O4 Nanoparticle Catalysts for the Microwave-Assisted Synthesis of Thioglyoxamides. ACS Applied Nano Materials 2023, 6 (5) , 4005-4016. https://doi.org/10.1021/acsanm.3c00324
2. Anastasia S. Kostyuchenko, Evgenii B. Uliankin, Anton J. Stasyuk, Anna L. Samsonenko, Tatyana Yu Zheleznova, Anton L. Shatsauskas, Alexander S. Fisyuk. Photochemical Synthesis and Electrochemical and Photophysical Properties of 2,7-Diarylbenzo[1,2-d:4,3-d′]bis(thiazoles). The Journal of Organic Chemistry 2022, 87 (10) , 6657-6667. https://doi.org/10.1021/acs.joc.2c00310
3. Ya-Qing Huang, Xiong-Zhi Huang, Pei-Qiang Huang. Synthesis of 5-(1-Alkoxyalkylidene)tetronates by Direct Condensation Reactions of Tetronates with Thionolactones and Thionoesters. The Journal of Organic Chemistry 2021, 86 (3) , 2359-2368. https://doi.org/10.1021/acs.joc.0c02502
4. Yuji Sasanuma, Syuto Tanaka. Molecular Design of Aromatic Polythionoesters. ACS Omega 2020, 5 (6) , 3016-3029. https://doi.org/10.1021/acsomega.9b04111
5. Sinenhlanhla N. Mthembu, Anamika Sharma, Fernando Albericio, Beatriz G. de la Torre. 2-(Dibenzylamino)butane-1,4-dithiol (DABDT), a Friendly Disulfide-Reducing Reagent Compatible with a Broad Range of Solvents. Organic Letters 2019, 21 (24) , 10111-10114. https://doi.org/10.1021/acs.orglett.9b04106
6. Paniz Pahlavanlu, Andrew J. Tilley, Bryony T. McAllister, Dwight S. Seferos. Microwave Synthesis of Thionated Naphthalene Diimide-Based Small Molecules and Polymers. The Journal of Organic Chemistry 2017, 82 (23) , 12337-12345. https://doi.org/10.1021/acs.joc.7b02162
7. L. Legnani, L. Toma, P. Caramella, M. A. Chiacchio, S. Giofrè, I. Delso, T. Tejero, and P. Merino . Computational Mechanistic Study of Thionation of Carbonyl Compounds with Lawesson’s Reagent. The Journal of Organic Chemistry 2016, 81 (17) , 7733-7740. https://doi.org/10.1021/acs.joc.6b01420
8. Inês L. Martins, Catarina Charneira, Valentina Gandin, João L. Ferreira da Silva, Gonçalo C. Justino, João P. Telo, Abel J. S. C. Vieira, Cristina Marzano, and Alexandra M. M. Antunes . Selenium-Containing Chrysin and Quercetin Derivatives: Attractive Scaffolds for Cancer Therapy. Journal of Medicinal Chemistry 2015, 58 (10) , 4250-4265. https://doi.org/10.1021/acs.jmedchem.5b00230
9. Jacques Rouden, Marie-Claire Lasne, Jérôme Blanchet, and Jérôme Baudoux . (−)-Cytisine and Derivatives: Synthesis, Reactivity, and Applications. Chemical Reviews 2014, 114 (1) , 712-778. https://doi.org/10.1021/cr400307e
10. Peter Hrobárik, Veronika Hrobáriková, Ivica Sigmundová, Pavol Zahradník, Mihalis Fakis, Ioannis Polyzos, and Peter Persephonis . Benzothiazoles with Tunable Electron-Withdrawing Strength and Reverse Polarity: A Route to Triphenylamine-Based Chromophores with Enhanced Two-Photon Absorption. The Journal of Organic Chemistry 2011, 76 (21) , 8726-8736. https://doi.org/10.1021/jo201411t
11. Philipp A. Ottersbach, Paul W. Elsinghorst, Hans-Georg Häcker and Michael Gütschow. Direct Formation of Ring-Fused 1,3-Thiazine-2,4-dithiones from Aromatic o-Amino Carboxylic Acids: Observation of a Carbon Disulfide Mediated Thionation. Organic Letters 2010, 12 (16) , 3662-3665. https://doi.org/10.1021/ol101471g
12. Qiuping Ding, Xi-Gen Huang and Jie Wu . Facile Synthesis of Benzothiazoles via Cascade Reactions of 2-Iodoanilines, Acid Chlorides and Lawesson’s Reagent. Journal of Combinatorial Chemistry 2009, 11 (6) , 1047-1049. https://doi.org/10.1021/cc900085p
13. Vaibhav Pravinchandra Mehta,, Anuj Sharma,, Kristof Van Hecke,, Luc Van Meervelt, and, Erik Van der Eycken. A Novel and Versatile Entry to Asymmetrically Substituted Pyrazines. The Journal of Organic Chemistry 2008, 73 (6) , 2382-2388. https://doi.org/10.1021/jo702656v
14. Turan Ozturk,, Erdal Ertas, and, Olcay Mert. Use of Lawesson's Reagent in Organic Syntheses. Chemical Reviews 2007, 107 (11) , 5210-5278. https://doi.org/10.1021/cr040650b
15. Zoltán Kaleta,, Gábor Tárkányi,, Ágnes Gömöry,, Ferenc Kálmán,, Tamás Nagy, and, Tibor Soós. Synthesis and Application of a Fluorous Lawesson's Reagent:  Convenient Chromatography-Free Product Purification. Organic Letters 2006, 8 (6) , 1093-1095. https://doi.org/10.1021/ol0529849
16. André B. Charette and, Michel Grenon. Mild Method for the Conversion of Amides to Thioamides. The Journal of Organic Chemistry 2003, 68 (14) , 5792-5794. https://doi.org/10.1021/jo0344485
17. Manel Querol,, Helen Stoekli-Evans, and, Peter Belser. 4,5-Diazafluorene-Based Overcrowded Alkene:  A New Ligand for Transition Metal Complexes. Organic Letters 2002, 4 (7) , 1067-1070. https://doi.org/10.1021/ol017130c
18. Andrzej Bak, Violetta Kozik, Aleksandra Swietlicka, Wojciech Baran, Adam Smolinski, Andrzej Zięba. Towards Symmetric Thioamides: Microwave-Aided Synthesis of Terephthalic Acid Derivatives. Pharmaceuticals 2023, 16 (7) , 984. https://doi.org/10.3390/ph16070984
19. Piotr Matczak, Sławomir Domagała, Wolfgang Weigand, Grzegorz Mlostoń. A comparative analysis of UV–vis transitions in hetaryl and ferrocenyl thioketones. Chemical Physics 2023, 570 , 111901. https://doi.org/10.1016/j.chemphys.2023.111901
20. Sodeeq Aderotimi Salami, Vincent J. Smith, Rui W. M. Krause. Aqueous microwave assisted novel synthesis of isothiocyanates by amine catalyzed thionation of isocyanides with Lawesson's reagent. Journal of Sulfur Chemistry 2023, 44 (3) , 269-281. https://doi.org/10.1080/17415993.2022.2164196
21. Mohamed S. Gomaa, Gaber El Enany, Walid Fathalla, Ibrahim A. I. Ali, Samir. M. El Rayes. Transformation of Amides to Thioamides Using an Efficient and Novel Thiating Reagent. Molecules 2022, 27 (23) , 8275. https://doi.org/10.3390/molecules27238275
22. Alena V. Koval’skaya, Polina R. Petrova, Dmitry O. Tsypyshev, Alexander N. Lobov, Inna P. Tsypysheva. Thionation of quinolizidine alkaloids and their derivatives via Lawesson’s reagent. Natural Product Research 2022, 36 (14) , 3538-3543. https://doi.org/10.1080/14786419.2020.1868460
23. Siji Thonivalappil Bhaskaran, Paulson Mathew. Microwave assisted synthesis of functionalized 2H-chromene-2-thiones and 1,2-dithiole-3-thiones from β-oxodithioesters: Characterization, in vitro cytotoxicity and in silico docking studies. Journal of Molecular Structure 2022, 1251 , 132071. https://doi.org/10.1016/j.molstruc.2021.132071
24. Navjeet Kaur. Thiazole Synthesis by Thionation of C=O to C=S. 2022, 63-114. https://doi.org/10.1007/978-981-16-4655-3_3
25. Navjeet Kaur. Thiadiazole Synthesis. 2022, 115-147. https://doi.org/10.1007/978-981-16-4655-3_4
26. Matthew D. Goodwin, Meggin Q. Costa, Jerome R. Robinson, Christopher M. Kotyk. Mechanochemical synthesis of thiolactams and other thioamides using Lawesson’s reagent. Results in Chemistry 2022, 4 , 100528. https://doi.org/10.1016/j.rechem.2022.100528
27. Matthew D. Goodwin, Meggin Q. Costa, Jerome R. Robinson, Christopher M. Kotyk. Mechanochemical Synthesis of Thiolactams and Other Thioamides Using Lawesson's Reagent. SSRN Electronic Journal 2022, 49 https://doi.org/10.2139/ssrn.4164026
28. Matthew D. Goodwin, Meggin Q. Costa, Jerome R. Robinson, Christopher M. Kotyk. Mechanochemical Synthesis of Thiolactams and Other Thioamides Using Lawesson's Reagent. SSRN Electronic Journal 2022, 49 https://doi.org/10.2139/ssrn.4199921
29. Matthew D. Goodwin, Meggin Q. Costa, Jerome R. Robinson, Christopher M. Kotyk. Mechanochemical Synthesis of Thiolactams and Other Thioamides Using Lawesson's Reagent. SSRN Electronic Journal 2022, 49 https://doi.org/10.2139/ssrn.4199922
30. Mohd. Tauqeer, Abhinav Raghuvanshi, Suman Ara Mazid, Saurabh Kumar Singh, Radhe Shyam Ji. Synthesis of [(CO)5MS=CFcCH3] and exploration of the nature of M-S vs. M-O bonds in [(CO)5ME=CFcCH3]; (M = Cr, Mo, W and E = O, S) complexes. Journal of Organometallic Chemistry 2021, 954-955 , 122080. https://doi.org/10.1016/j.jorganchem.2021.122080
31. Hena Khatoon, Emilia Abdulmalek. A Focused Review of Synthetic Applications of Lawesson’s Reagent in Organic Synthesis. Molecules 2021, 26 (22) , 6937. https://doi.org/10.3390/molecules26226937
32. Aparna Das, Muhammad Waqar Ashraf, Bimal Krishna Banik. Thione Derivatives as Medicinally Important Compounds. ChemistrySelect 2021, 6 (34) , 9069-9100. https://doi.org/10.1002/slct.202102398
33. Long Huang, Xuehui Liu, Duntie Zhang, Chenghao Luo, Jing Zhang, Yikun Chen, Yuefa Gong. A straightforward route to alkyl 5‐arylthiophene ‐2‐thiocarboxylates from alkyl 2‐aroyl ‐1‐chlorocyclopropanecarboxylates. Journal of Heterocyclic Chemistry 2021, 58 (3) , 882-891. https://doi.org/10.1002/jhet.4225
34. . Miscellaneous Reactions. 2021, 161-291. https://doi.org/10.1002/9783527828166.ch4
35. Krishnanka Shekhar Gayen, Nirbhik Chatterjee. Diversity of Lawesson's Reagent: Advances and Scope. Asian Journal of Organic Chemistry 2020, 9 (4) , 508-528. https://doi.org/10.1002/ajoc.202000032
36. Nhan T. Do, Khoa M. Tran, Hao T. Phan, Tuong A. To, Tung T. Nguyen, Nam T. S. Phan. Functionalization of activated methylene C–H bonds with nitroarenes and sulfur for the synthesis of thioamides. Organic & Biomolecular Chemistry 2019, 17 (40) , 8987-8991. https://doi.org/10.1039/C9OB01751H
37. Xiangjun Peng, Feng Qin, Mengyue Xu, Shaojie Zhu, Yingming Pan, Haitao Tang, Xiujin Meng, Hengshan Wang. Synthesis of imidazo[1,2- c ]thiazoles through Pd-catalyzed bicyclization of tert -butyl isonitrile with thioamides. Organic & Biomolecular Chemistry 2019, 17 (36) , 8403-8407. https://doi.org/10.1039/C9OB01664C
38. Elena Cini, Maurizio Taddei. Microwave Dielectric Heating for Solvent-free Organic Transformations. 2019, 216-244. https://doi.org/10.1039/9781788016131-00216
39. Wei Guo, Kailiang Tao, Wen Tan, Mingming Zhao, Lvyin Zheng, Xiaolin Fan. Recent advances in photocatalytic C–S/P–S bond formation via the generation of sulfur centered radicals and functionalization. Organic Chemistry Frontiers 2019, 6 (12) , 2048-2066. https://doi.org/10.1039/C8QO01353E
40. Saber Ghafari Nikoo Jooneghani, Alireza Gholipour. Mutual cooperation of π-π stacking and pnicogen bond interactions of substituted monomeric Lawesson’s reagent and pyridine rings: Theoretical insight into Pyr||X-PhPS2⊥pyr complexes. Chemical Physics Letters 2019, 721 , 91-98. https://doi.org/10.1016/j.cplett.2019.02.027
41. Carla Júnia Santos, Daniel Crístian Ferreira Soares, Carolina de Aguiar Ferreira, André Luís Branco de Barros, Armando da Silva Cunha Junior, Francisco Moura Filho. Antiangiogenic evaluation of ZnWO 4 nanoparticles synthesised through microwave-assisted hydrothermal method. Journal of Drug Targeting 2018, 26 (9) , 806-817. https://doi.org/10.1080/1061186X.2018.1428810
42. Toshiaki Murai. The Construction and Application of C=S Bonds. Topics in Current Chemistry 2018, 376 (4) https://doi.org/10.1007/s41061-018-0209-0
43. Xu Yan, Guan Wang, Li-Hua Zhang, Li Wang, Xiao-Fei Liu, Wan-Tai Yang. Thioxanthene-9-thione Mediated MMA Polymerization. Chinese Journal of Polymer Science 2018, 36 (7) , 805-810. https://doi.org/10.1007/s10118-018-2140-9
44. Yohei Matsumoto, Daiki Nakatake, Ryo Yazaki, Takashi Ohshima. An Expeditious Route to trans ‐Configured Tetrahydrothiophenes Enabled by Fe(OTf) 3 ‐Catalyzed [3+2] Cycloaddition of Donor–Acceptor Cyclopropanes with Thionoesters. Chemistry – A European Journal 2018, 24 (23) , 6062-6066. https://doi.org/10.1002/chem.201800957
45. Aamer Saeed, Haroon Mehfooz, Fayaz Ali Larik, Muhammad Faisal, Pervaiz Ali Channar. Applications of Lawesson’s reagent in the synthesis of naturally occurring steroids and terpenoids. Journal of Asian Natural Products Research 2017, 19 (11) , 1114-1123. https://doi.org/10.1080/10286020.2017.1295229
46. Yuttapong Singjunla, Morgane Pigeaux, Romain Laporte, Jérôme Baudoux, Jacques Rouden. Thioamide‐Substituted Cinchona Alkaloids as Efficient Organocatalysts for Asymmetric Decarboxylative Reactions of MAHOs. European Journal of Organic Chemistry 2017, 2017 (29) , 4319-4323. https://doi.org/10.1002/ejoc.201700870
47. Wei Li, Xueli Li, Manhui Liu, Qiuan Wang. Synthesis and Antiproliferative Activity of Thioxoflavones Mannich Base Derivatives. Archiv der Pharmazie 2017, 350 (7) https://doi.org/10.1002/ardp.201700044
48. Grzegorz Mlostoń, Paulina Grzelak, Anthony Linden, Heinz Heimgartner. Thia-Diels–Alder reactions of hetaryl thioketones with nonactivated 1,3-dienes leading to 3,6-dihydro-2H-pyrans: evidence for a diradical mechanism. Chemistry of Heterocyclic Compounds 2017, 53 (5) , 518-525. https://doi.org/10.1007/s10593-017-2086-9
49. Shanshan Zhong, Yunyun Liu, Xiaoji Cao, Jie‐Ping Wan. KIO 3 ‐Catalyzed Domino C(sp 2 )−H Bond Sulfenylation and C−N Bond Oxygenation of Enaminones toward the Synthesis of 3‐Sulfenylated Chromones. ChemCatChem 2017, 9 (3) , 465-468. https://doi.org/10.1002/cctc.201601273
50. Tamashree Ghosh, Anshupriya Si, Anup Kumar Misra. Facile Transformation of Nitriles into Thioamides: Application to C ‐Glycosyl Nitrile Derivatives. ChemistrySelect 2017, 2 (4) , 1366-1369. https://doi.org/10.1002/slct.201601984
51. Róża Hamera-Fałdyga, Paulina Grzelak, Paulina Pipiak, Grzegorz Mlostoń. Microwave assisted synthesis of ferrocenyl and hetaryl functionalized thioketones. Phosphorus, Sulfur, and Silicon and the Related Elements 2017, 192 (2) , 197-198. https://doi.org/10.1080/10426507.2016.1252367
52. Kazuhiro Kobayashi, Hiroki Inouchi, Ryo Hasegawa, Kazuki Kawano. Synthesis of 3-(Alkylsulfanyl)-1,4-benzothiazine Derivatives Based on Cyclization of 2-[(Cyanomethyl)sulfanyl]phenyl Isothiocyanate. HETEROCYCLES 2017, 94 (12) , 2307. https://doi.org/10.3987/COM-17-13823
53. Paulina Grzelak, Grzegorz Mlostoń. Applications of thiobenzophenone for the synthesis of 3-, 4-, 5-, and 6-membered sulfur heterocycles (microreview). Chemistry of Heterocyclic Compounds 2016, 52 (5) , 282-284. https://doi.org/10.1007/s10593-016-1878-7
54. Marwa Gardelly, Belsem Trimech, Mohamed Amine Belkacem, Mounira Harbach, Soukaina Abdelwahed, Amor Mosbah, Jalloul Bouajila, Hichem Ben Jannet. Synthesis of novel diazaphosphinanes coumarin derivatives with promoted cytotoxic and anti-tyrosinase activities. Bioorganic & Medicinal Chemistry Letters 2016, 26 (10) , 2450-2454. https://doi.org/10.1016/j.bmcl.2016.03.108
55. Patrick G. McCaw, Naomi M. Buckley, Stuart G. Collins, Anita R. Maguire. Generation, Reactivity and Uses of Sulfines in Organic Synthesis. European Journal of Organic Chemistry 2016, 2016 (9) , 1630-1650. https://doi.org/10.1002/ejoc.201501538
56. Hong-Zheng Li, Wei-Jian Xue, Guo-Dong Yin, An-Xin Wu. A multipathway coupled domino strategy: I2-mediated oxidative thionation for direct synthesis of thiobenzamides from miscellaneous substrates. Tetrahedron Letters 2015, 56 (43) , 5843-5846. https://doi.org/10.1016/j.tetlet.2015.08.060
57. Ko Hoon Kim, Hye Ran Moon, Junseong Lee, Jimin Kim, Jae Nyoung Kim. Diastereoselective Synthesis of Six‐Membered Carbocyclic Spirooxindoles via 6π‐Electrocyclization of 3‐Dienylidene‐2‐ oxindoles. Advanced Synthesis & Catalysis 2015, 357 (7) , 1532-1544. https://doi.org/10.1002/adsc.201500260
58. Ko Hoon Kim, Hye Ran Moon, Junseong Lee, Jae Nyoung Kim. Palladium‐Catalyzed Construction of Spirooxindoles by Arylative Cyclization of 3‐(γ,δ‐Disubstituted)allylidene‐2‐Oxindoles. Advanced Synthesis & Catalysis 2015, 357 (4) , 701-708. https://doi.org/10.1002/adsc.201400965
59. L. A. Kayukova, K. D. Praliyev, V. G. Gut’yar, G. P. Baitursynova. Modification of organic compounds with Lawesson’s reagent. Russian Journal of Organic Chemistry 2015, 51 (2) , 148-160. https://doi.org/10.1134/S1070428015020025
60. Hye Ran Moon, Ko Hoon Kim, Junseong Lee, Jae Nyoung Kim. Synthesis of 3‐(γ,δ‐Disubstituted)allylidene‐2‐Oxindoles from Isatins by Wittig Reaction with Morita–Baylis–Hillman Bromides. Bulletin of the Korean Chemical Society 2015, 36 (1) , 219-225. https://doi.org/10.1002/bkcs.10053
61. Sébastien Redon, Youssef Kabri, Maxime D. Crozet, Patrice Vanelle. One-pot preparation of 2-(alkyl)arylbenzoselenazoles from the corresponding N-(acetyl)benzoyl-2-iodoanilines via a microwave-assisted methodology. Tetrahedron Letters 2014, 55 (36) , 5052-5054. https://doi.org/10.1016/j.tetlet.2014.07.055
62. Hong-Zheng Li, Wei-Jian Xue, An-Xin Wu. Direct synthesis of α-ketothioamides from aryl methyl ketones and amines via I2-promoted sp3 C–H functionalization. Tetrahedron 2014, 70 (31) , 4645-4651. https://doi.org/10.1016/j.tet.2014.05.045
63. Andreas Gebert, Marcin Jasiński, Grzegorz Mlostoń, Heinz Heimgartner. Reduction of Thiocarbonyl Compounds with Lithium Diisopropylamide. Helvetica Chimica Acta 2014, 97 (7) , 931-938. https://doi.org/10.1002/hlca.201400130
64. Anirudha A. Waghmare, Rama Mohan Hindupur, Hari N. Pati. Propylphosphonic anhydride (T3P®): An expedient reagent for organic synthesis. Review Journal of Chemistry 2014, 4 (2) , 53-131. https://doi.org/10.1134/S2079978014020034
65. Inês Martins, Joana Miranda, Nuno Oliveira, Ana Fernandes, Sandrina Gonçalves, Alexandra Antunes. Synthesis and Biological Activity of 6-Selenocaffeine: Potential Modulator of Chemotherapeutic Drugs in Breast Cancer Cells. Molecules 2013, 18 (5) , 5251-5264. https://doi.org/10.3390/molecules18055251
66. Rajender S. Varma. Microwave Technology—Applications in Chemical Synthesis. 2013, 1-68. https://doi.org/10.1002/0471238961.1309031822011813.a01.pub2
67. Rajender S. Varma. Green Chemistry with Microwave Energy. 2013, 115-156. https://doi.org/10.1007/978-1-4614-5817-3_5
68. Manoj B. Gawande, Vasco D. B. Bonifácio, Rafael Luque, Paula S. Branco, Rajender S. Varma. Benign by design: catalyst-free in-water, on-water green chemical methodologies in organic synthesis. Chemical Society Reviews 2013, 42 (12) , 5522. https://doi.org/10.1039/c3cs60025d
69. Marwa Sayed Salem, Magda Ismail Marzouk, Salma Nasser Ali, Hassan Mohamed Fawzy Madkour. Synthesis, structure characterization and biological evaluation of new 6,8-dichloro-2-methyl-4H-chromen-4-one derivatives. European Journal of Chemistry 2012, 3 (2) , 220-227. https://doi.org/10.5155/eurjchem.3.2.220-227.592
70. Lynn James Guziec, Frank S. Guziec. Twofold Extrusion Reactions. 2012, 411-550. https://doi.org/10.1002/0471264180.or078.03
71. Namjin Park, Yumi Heo, Manian Rajesh Kumar, Yong Kim, Kwang Ho Song, Sunwoo Lee. Synthesis of Benzothiazoles through Copper‐Catalyzed One‐Pot Three‐Component Reactions with Use of Sodium Hydrosulfide as a Sulfur Surrogate. European Journal of Organic Chemistry 2012, 2012 (10) , 1984-1993. https://doi.org/10.1002/ejoc.201101773
72. Lyudmila Kayukova, Kaldubai Praliyev, Ulan Kemelbekov, Asel Abdildanova, Vanda Gutyar. Interaction of the O-Benzoyl--aminopropioamidoximes with Lawesson's Reagent and Spectral Characterization of the Products. ISRN Organic Chemistry 2012, 2012 , 1-6. https://doi.org/10.5402/2012/945893
73. Jeong Heon Lee, Hoon Hyun, Conor J. Cross, Maged Henary, Khaled A. Nasr, Rafiou Oketokoun, Hak Soo Choi, John V. Frangioni. Rapid and Facile Microwave‐Assisted Surface Chemistry for Functionalized Microarray Slides. Advanced Functional Materials 2012, 22 (4) , 872-878. https://doi.org/10.1002/adfm.201102033
74. Rajender S. Varma. Green Chemistry with Microwave Energy. 2012, 4642-4673. https://doi.org/10.1007/978-1-4419-0851-3_238
75. Helen Rachel Lagiakos, Ashley Walker, Marie-Isabel Aguilar, Patrick Perlmutter. Thionation of amides using a solid-supported P2S5 reagent under microwave irradiation. Tetrahedron Letters 2011, 100 https://doi.org/10.1016/j.tetlet.2011.07.104
76. Anna Pawełczyk, Lucjusz Zaprutko. Synthesis of fragrant heterocyclic thioketo analogues of jasmone under microwave conditions. Flavour and Fragrance Journal 2011, 26 (2) , 101-106. https://doi.org/10.1002/ffj.2023
77. Guanyinsheng Qiu, Yi Hu, Qiuping Ding, Yiyuan Peng, Xiangzheng Hu, Jie Wu. Synthesis of 4-methylene-4H-benzo[d][1,3]thiazines via a tandem reaction of 1-(2-alkynylphenyl)ketoximes with Lawesson's reagent. Chemical Communications 2011, 47 (34) , 9708. https://doi.org/10.1039/c1cc12937f
78. . Lawesson's Reagent. 2010, 1722-1727. https://doi.org/10.1002/9780470638859.conrr386
79. Dongho Cho, Jiyoung Ahn, Kathlia A. De Castro, Hyunseok Ahn, Hakjune Rhee. P4S10/dimethicone tandem: efficient reagent for thionation of various aromatic amides and esters. Tetrahedron 2010, 66 (30) , 5583-5588. https://doi.org/10.1016/j.tet.2010.05.100
80. Natalija M. Krstić, Mira S. Bjelaković, Milan M. Dabović, Vladimir D. Pavlović. Thionation of Some α,β-Unsaturated Steroidal Ketones. Molecules 2010, 15 (5) , 3462-3477. https://doi.org/10.3390/molecules15053462
81. Hai-Ming Guo, Peng-Yang Xin, Hong-Ying Niu, Dong-Chao Wang, Yi Jiang, Gui-Rong Qu. Microwave irradiated C6-functionalization of 6-chloropurine nucleosides with various mild nucleophiles under solvent-free conditions. Green Chemistry 2010, 12 (12) , 2131. https://doi.org/10.1039/c0gc00517g
82. Tuyen Kim Pham Nguyen, Kim Phi Phung Nguyen, Fadhil S. Kamounah, Wei Zhang, Poul Erik Hansen. NMR of a series of novel hydroxyflavothiones. Magnetic Resonance in Chemistry 2009, 47 (12) , 1043-1054. https://doi.org/10.1002/mrc.2510
83. Yu Rao, Xuechen Li, Pavel Nagorny, Joji Hayashida, Samuel J. Danishefsky. A simple method for the conversion of carboxylic acids into thioacids with Lawesson’s reagent. Tetrahedron Letters 2009, 50 (48) , 6684-6686. https://doi.org/10.1016/j.tetlet.2009.09.080
84. John Kallikat Augustine, Veeramani Vairaperumal, Sharmila Narasimhan, Padma Alagarsamy, Anbarasi Radhakrishnan. Propylphosphonic anhydride (T3P®): an efficient reagent for the one-pot synthesis of 1,2,4-oxadiazoles, 1,3,4-oxadiazoles, and 1,3,4-thiadiazoles. Tetrahedron 2009, 65 (48) , 9989-9996. https://doi.org/10.1016/j.tet.2009.09.114
85. Tarek A. Salama, Abdel-Aziz S. El-Ahl, Saad S. Elmorsy, Abdel-Galil M. Khalil, Mohamed A. Ismail. A new convenient procedure for the thionation of carbonyl compounds utilizing tetrachlorosilane–sodium sulfide. Tetrahedron Letters 2009, 50 (43) , 5933-5936. https://doi.org/10.1016/j.tetlet.2009.08.039
86. Kadir Aslan, Chris D. Geddes. Metal-enhanced chemiluminescence: advanced chemiluminescence concepts for the 21st century. Chemical Society Reviews 2009, 38 (9) , 2556. https://doi.org/10.1039/b807498b
87. Aamer Saeed, Zaman Ashraf. Synthesis of some 3‐aryl‐1 H ‐isochromene‐1‐thiones. Journal of Heterocyclic Chemistry 2008, 45 (3) , 679-682. https://doi.org/10.1002/jhet.5570450307
88. Q. Qiao, R. Dominique, R. Goodnow. 2,4-Disubstituted-5-acetoxythiazoles: useful intermediates for the synthesis of thiazolones and 2,4,5-trisubstituted thiazoles. Tetrahedron Letters 2008, 49 (22) , 3682-3686. https://doi.org/10.1016/j.tetlet.2008.03.140
89. Miroslav Kvasnica, Iva Rudovska, Ivana Cisarova, Jan Sarek. Reaction of lupane and oleanane triterpenoids with Lawesson's reagent. Tetrahedron 2008, 64 (17) , 3736-3743. https://doi.org/10.1016/j.tet.2008.02.023
90. Alfredo Ricci. Solventless Reactions Under Microwave Activation: Safety and Efficiency at the Service of Customer-friendly Chemistry. 2008, 193-223. https://doi.org/10.1007/978-1-4020-6793-8_10
91. Fushun Liang, Yan Li, Dazhi Li, Xin Cheng, Qun Liu. A tandem reaction of 2-acetylmethylene-1,3-dithiolanes via fragmentation of the dithiolane ring in the presence of amines: a facile route to functionalized thioamides. Tetrahedron Letters 2007, 48 (45) , 7938-7941. https://doi.org/10.1016/j.tetlet.2007.09.065
92. Zdzislaw Paryzek, Iwona Skiera. SYNTHESIS AND CLEAVAGE OF LACTONES AND THIOLACTONES. APPLICATIONS IN ORGANIC SYNTHESIS. A REVIEW. Organic Preparations and Procedures International 2007, 39 (3) , 203-296. https://doi.org/10.1080/00304940709356015
93. Genevieve Etornam Adukpo, Tobias Borrmann, René Manski, Rosa I. Sáez Díaz, Wolf‐Dieter Stohrer, Franz‐Peter Montforts. Synthesis of an Enantiomerically Pure Building Block for the Synthesis of Hydroporphyrins. European Journal of Organic Chemistry 2007, 2007 (2) , 249-257. https://doi.org/10.1002/ejoc.200600656
94. Jürgen Voss, Jürgen Voss. 2,4-Bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane 2,4-Disulfide. 2006https://doi.org/10.1002/047084289X.rb170.pub2
95. Jarosław Spychała. Convenient syntheses of N-methylthioamides: A migration of the H 2 S molecule in the thioamide-nitrile system. Journal of Sulfur Chemistry 2006, 27 (3) , 203-212. https://doi.org/10.1080/17415990600654599
96. Gabriela Aguirre, Mariana Boiani, Eliana Cabrera, Hugo Cerecetto, Rossanna Di Maio, Mercedes González, Ana Denicola, Carlos Mauricio R. Sant’Anna, Eliezer J. Barreiro. New potent 5-nitrofuryl derivatives as inhibitors of Trypanosoma cruzi growth. 3D-QSAR (CoMFA) studies. European Journal of Medicinal Chemistry 2006, 41 (4) , 457-466. https://doi.org/10.1016/j.ejmech.2005.11.008
97. E.S.H. El Ashry, A.A. Kassem, E. Ramadan. Microwave Irradiation for Accelerating Organic Reactions – Part II: Six-, Seven-Membered, Spiro, and Fused Heterocycles. 2006, 1-123. https://doi.org/10.1016/S0065-2725(05)90001-9
98. D. V. Kuznetsov, V. A. Raev, G. L. Kuranov, O. V. Arapov, R. R. Kostikov. Microwave Activation in Organic Synthesis. Russian Journal of Organic Chemistry 2005, 41 (12) , 1719-1749. https://doi.org/10.1007/s11178-006-0030-z
99. L. Valette, S. Poulain, X. Fernandez, L. Lizzani-Cuvelier. Efficient and solvent-free microwave-accelerated synthesis of isothiocyanates using Lawesson’s reagent. Journal of Sulfur Chemistry 2005, 26 (2) , 155-161. https://doi.org/10.1080/17415990500070144
100. Ross S. Robinson, Martin C. Dovey, David Gravestock. Silver‐Catalyzed Hydroamination: Synthesis of N ‐Bridgehead Pyrroles, Incorporating a Protection‐Deprotection Strategy for Preparation of Cyclic Secondary Vinylogous Carbamates. European Journal of Organic Chemistry 2005, 2005 (3) , 505-511. https://doi.org/10.1002/ejoc.200400598