Статті в журналах з теми "Thiochromenes"
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Luque-Agudo, V., J. Albarrán-Velo, J. G. Fernández-Bolaños, O. López, M. E. Light, J. M. Padrón, I. Lagunes, E. Román, J. A. Serrano, and M. V. Gil. "Synthesis and antiproliferative activity of sulfa-Michael adducts and thiochromenes derived from carbohydrates." New Journal of Chemistry 41, no. 8 (2017): 3154–62. http://dx.doi.org/10.1039/c6nj03940e.
Повний текст джерелаOrtiz, Cristian, Fernando Echeverri, Sara Robledo, Daniela Lanari, Massimo Curini, Wiston Quiñones, and Esteban Vargas. "Synthesis and Evaluation of Antileishmanial and Cytotoxic Activity of Benzothiopyrane Derivatives." Molecules 25, no. 4 (February 12, 2020): 800. http://dx.doi.org/10.3390/molecules25040800.
Повний текст джерелаAn, Yi, Fang Zhang, Guangfen Du, Zhihua Cai, and Lin He. "Construction of 6H-benzo[c]thiochromenes via a tandem reaction of arynes with thionoesters." Organic Chemistry Frontiers 8, no. 24 (2021): 6979–84. http://dx.doi.org/10.1039/d1qo01177d.
Повний текст джерелаChanda, Rupsa, Abhishek Kar, Aniruddha Das, Baitan Chakraborty та Umasish Jana. "Iron-catalyzed carboarylation of alkynes via activation of π-activated alcohols: rapid synthesis of substituted benzofused six-membered heterocycles". Organic & Biomolecular Chemistry 19, № 23 (2021): 5155–60. http://dx.doi.org/10.1039/d1ob00488c.
Повний текст джерелаWang, W., H. Li, J. Wang, and L. Zu. "Organocatalytic One-Pot Synthesis of Chiral Thiochromenes." Synfacts 2006, no. 10 (September 2006): 1065. http://dx.doi.org/10.1055/s-2006-949371.
Повний текст джерелаMarkova, L. I., and V. G. Kharchenko. "Specific reactions of 5-oxotetrahydro-4H-thiochromenes with Grignard reagents." Chemistry of Heterocyclic Compounds 30, no. 5 (May 1994): 537–39. http://dx.doi.org/10.1007/bf01169828.
Повний текст джерелаGabbutt, Christopher D., John D. Hepworth, and B. Mark Heron. "Reactions of some 2H-Chromenes and 2H-Thiochromenes with triazolinediones." Tetrahedron 51, no. 48 (November 1995): 13277–90. http://dx.doi.org/10.1016/0040-4020(95)00874-8.
Повний текст джерелаBhanja, Chittaranjan, Satyaban Jena, Sabita Nayak, and Seetaram Mohapatra. "Organocatalytic tandem Michael addition reactions: A powerful access to the enantioselective synthesis of functionalized chromenes, thiochromenes and 1,2-dihydroquinolines." Beilstein Journal of Organic Chemistry 8 (October 4, 2012): 1668–94. http://dx.doi.org/10.3762/bjoc.8.191.
Повний текст джерелаTércio, J., B. Ferreira, V. Catani, and J. V. Comasseto. "Synthesis of 2,2-Dimethyl-2H-thiochromenes, the Sulfur Analogs of Precocenes." Synthesis 1987, no. 02 (1987): 149–53. http://dx.doi.org/10.1055/s-1987-27866.
Повний текст джерелаVoskressensky, Leonid G., Ekaterina A. Sokolova, Alexey A. Festa, and Alexey V. Varlamov. "A novel domino condensation–intramolecular nucleophilic cyclization approach towards annulated thiochromenes." Tetrahedron Letters 54, no. 38 (September 2013): 5172–73. http://dx.doi.org/10.1016/j.tetlet.2013.07.040.
Повний текст джерелаAhlemeyer, Nicholas A., and Vladimir B. Birman. "Asymmetric Catalytic Synthesis of Thiochromenes via an Acyl Transfer-Initiated Cascade." Organic Letters 18, no. 14 (July 6, 2016): 3454–57. http://dx.doi.org/10.1021/acs.orglett.6b01639.
Повний текст джерелаWang, Wei, Hao Li, Jian Wang, and Liansuo Zu. "Enantioselective Organocatalytic Tandem Michael−Aldol Reactions: One-Pot Synthesis of Chiral Thiochromenes." Journal of the American Chemical Society 128, no. 32 (August 2006): 10354–55. http://dx.doi.org/10.1021/ja063328m.
Повний текст джерелаGabbutt, Christopher D., David J. Hartley, John D. Hepworth, B. Mark Heron, Magan Kanjia, and M. Moshfiqur Rahman. "Synthesis and reactivity of some 4-bromo- 2H-chromenes and 2H-thiochromenes." Tetrahedron 50, no. 8 (February 1994): 2507–22. http://dx.doi.org/10.1016/s0040-4020(01)86967-2.
Повний текст джерелаGABBUTT, C. D., J. D. HEPWORTH, and B. M. HERON. "ChemInform Abstract: Reactions of Some 2H-Chromenes and 2H-Thiochromenes with Triazolinediones." ChemInform 27, no. 13 (August 12, 2010): no. http://dx.doi.org/10.1002/chin.199613145.
Повний текст джерелаMuthupandi, Pandi, Nallappan Sundaravelu, and Govindasamy Sekar. "Domino Synthesis of Thiochromenes through Cu-Catalyzed Incorporation of Sulfur Using Xanthate Surrogate." Journal of Organic Chemistry 82, no. 4 (February 6, 2017): 1936–42. http://dx.doi.org/10.1021/acs.joc.6b02740.
Повний текст джерелаMarkova, L. I., N. G. Korobochkina, and V. G. Kharchenko. "Unusual conversion of substituted 5-oxo-5,6,7,8-tetrahydro-4H-thiochromenes with phosphorus pentachloride." Chemistry of Heterocyclic Compounds 35, no. 6 (June 1999): 746–47. http://dx.doi.org/10.1007/bf02251637.
Повний текст джерелаChoudhury, Abhijnan Ray, and Santanu Mukherjee. "A Catalytic Michael/Horner-Wadsworth-Emmons Cascade Reaction for Enantioselective Synthesis of Thiochromenes." Advanced Synthesis & Catalysis 355, no. 10 (July 8, 2013): 1989–95. http://dx.doi.org/10.1002/adsc.201300281.
Повний текст джерелаVoskressensky, Leonid G., Ekaterina A. Sokolova, Alexey A. Festa, and Alexey V. Varlamov. "ChemInform Abstract: A Novel Domino Condensation-Intramolecular Nucleophilic Cyclization Approach Towards Annulated Thiochromenes." ChemInform 45, no. 3 (January 2, 2014): no. http://dx.doi.org/10.1002/chin.201403181.
Повний текст джерелаVelasco, Noelia, Anisley Suárez, Fernando Martínez-Lara, Manuel Ángel Fernández-Rodríguez, Roberto Sanz, and Samuel Suárez-Pantiga. "From Propargylic Alcohols to Substituted Thiochromenes: gem-Disubstituent Effect in Intramolecular Alkyne Iodo/hydroarylation." Journal of Organic Chemistry 86, no. 10 (April 30, 2021): 7078–91. http://dx.doi.org/10.1021/acs.joc.1c00333.
Повний текст джерелаMARKOVA, L. I., and V. G. KHARCHENKO. "ChemInform Abstract: Peculiarities in the Reaction of 5-Oxotetrahydro-4H-thiochromenes with Grignard Reagents." ChemInform 26, no. 10 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199510158.
Повний текст джерелаGABBUTT, C. D., D. J. HARTLEY, J. D. HEPWORTH, B. M. HERON, M. KANJIA, and M. M. RAHMAN. "ChemInform Abstract: Synthesis and Reactivity of Some 4-Bromo-2H-chromenes and -2H- thiochromenes." ChemInform 25, no. 26 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199426166.
Повний текст джерелаSimlandy, Amit Kumar, and Santanu Mukherjee. "Catalytic Enantioselective Synthesis of 3,4-Unsubstituted Thiochromenes through Sulfa-Michael/Julia–Kocienski Olefination Cascade Reaction." Journal of Organic Chemistry 82, no. 9 (April 19, 2017): 4851–58. http://dx.doi.org/10.1021/acs.joc.7b00579.
Повний текст джерелаMarkova, L. I., N. G. Korobochkina, and V. G. Kharchenko. "ChemInform Abstract: Unusual Conversion of Substituted 5-Oxo-5,6,7,8-tetrahydro-4H-thiochromenes with Phosphorus Pentachloride." ChemInform 31, no. 18 (June 8, 2010): no. http://dx.doi.org/10.1002/chin.200018095.
Повний текст джерелаChoudhury, Abhijnan Ray, and Santanu Mukherjee. "ChemInform Abstract: A Catalytic Michael/Horner-Wadsworth-Emmons Cascade Reaction for Enantioselective Synthesis of Thiochromenes." ChemInform 44, no. 50 (November 21, 2013): no. http://dx.doi.org/10.1002/chin.201350159.
Повний текст джерелаCui, Sun-Liang, Jing Wang, and Yan-Guang Wang. "Efficient synthesis of 2-imino-1,2-dihydroquinolines and 2-imino-thiochromenes via copper-catalyzed domino reaction." Tetrahedron 64, no. 3 (January 2008): 487–92. http://dx.doi.org/10.1016/j.tet.2007.11.025.
Повний текст джерелаCha, Myeong Jong, Young Seok Song, Eun‐Gu Han, and Kee‐Jung Lee. "Application of the acetate of baylis‐hillman adducts in the synthesis of 3‐carbomethoxy‐2H‐thiochromenes." Journal of Heterocyclic Chemistry 45, no. 1 (January 2008): 235–40. http://dx.doi.org/10.1002/jhet.5570450129.
Повний текст джерелаLiu, Tong, Guanyinsheng Qiu, Qiuping Ding, and Jie Wu. "Assembly of 3-(trifluoromethyl)thiochromenes via a regioselective trifluoromethylthioarylation of (3-arylprop-2-ynyl)oxybenzenes with trifluoromethanesulfanylamide." Tetrahedron 72, no. 11 (March 2016): 1472–76. http://dx.doi.org/10.1016/j.tet.2016.01.053.
Повний текст джерелаKinfe, Henok Hadgu, Fanuel Mesfin Mebrahtu, Felix Loka Makolo, Paseka Thendo Moshapo та Mandlenkosi Maxwell Manana. "Stereoselective Synthesis of Thiochromenes via Intramolecular Tandem Thio-Michael Addition of in Situ Generated α,β-Unsaturated Aldehydes". Journal of Organic Chemistry 79, № 7 (18 березня 2014): 3111–18. http://dx.doi.org/10.1021/jo5002164.
Повний текст джерелаWang, Dan-Jiao, Zhuang Hou, Hang Xu, Ran An, Xin Su, and Chun Guo. "Design, synthesis, and biological evaluation of 4-chloro-2H-thiochromenes featuring nitrogen-containing side chains as potent antifungal agents." Bioorganic & Medicinal Chemistry Letters 28, no. 22 (December 2018): 3574–78. http://dx.doi.org/10.1016/j.bmcl.2018.06.035.
Повний текст джерелаKinfe, Henok Hadgu, Fanuel Mesfin Mebrahtu, Felix Loka Makolo, Paseka Thendo Moshapo та Mandlenkosi Maxwell Manana. "ChemInform Abstract: Stereoselective Synthesis of Thiochromenes via Intramolecular Tandem Thio-Michael Addition of in situ Generated α,β-Unsaturated Aldehydes." ChemInform 45, № 39 (11 вересня 2014): no. http://dx.doi.org/10.1002/chin.201439168.
Повний текст джерелаPham, Chien Thang, Dinh Hung Mac, and Thai Thanh Thu Bui. "Crystal structures of 2-(2-bromo-5-fluorophenyl)-8-ethoxy-3-nitro-2H-thiochromene and 2-(2-bromo-5-fluorophenyl)-7-methoxy-3-nitro-2H-thiochromene." Acta Crystallographica Section E Crystallographic Communications 75, no. 11 (October 31, 2019): 1783–86. http://dx.doi.org/10.1107/s2056989019014178.
Повний текст джерелаBhanja, Chittaranjan, Satyaban Jena, Sabita Nayak, and Seetaram Mohapatra. "ChemInform Abstract: Organocatalytic Tandem Michael Addition Reactions: A Powerful Access to the Enantioselective Synthesis of Functionalized Chromenes, Thiochromenes and 1,2-Dihydroquinolines." ChemInform 44, no. 12 (March 14, 2013): no. http://dx.doi.org/10.1002/chin.201312246.
Повний текст джерелаBarakat, Assem, Mohammad Shahidul Islam, M. Ali, Abdullah Mohammed Al-Majid, Saeed Alshahrani, Abdullah Saleh Alamary, Sammer Yousuf, and M. Iqbal Choudhary. "Regio- and Stereoselective Synthesis of a New Series of Spirooxindole Pyrrolidine Grafted Thiochromene Scaffolds as Potential Anticancer Agents." Symmetry 13, no. 8 (August 4, 2021): 1426. http://dx.doi.org/10.3390/sym13081426.
Повний текст джерелаRoy, Rimi, Soumyadipta Rakshit, Tanmoy Bhowmik, Sagar Khan, Avishek Ghatak, and Sanjay Bhar. "Substituted 3-E-Styryl-2H-chromenes and 3-E-Styryl-2H-thiochromenes: Synthesis, Photophysical Studies, Anticancer Activity, and Exploration to Tricyclic Benzopyran Skeleton." Journal of Organic Chemistry 79, no. 14 (July 7, 2014): 6603–14. http://dx.doi.org/10.1021/jo5011125.
Повний текст джерелаUsachev, B. I., M. A. Shafeev, and V. Ya Sosnovskikh. "2-Trif luoromethyl-4H-thiochromen-4-one and 2-trif luoromethyl-4H-thiochromene-4-thione: Synthesis and reactivities." Russian Chemical Bulletin 55, no. 3 (March 2006): 523–28. http://dx.doi.org/10.1007/s11172-006-0286-z.
Повний текст джерелаRoy, Rimi, Soumyadipta Rakshit, Tanmoy Bhowmik, Sagar Khan, Avishek Ghatak, and Sanjay Bhar. "ChemInform Abstract: Substituted 3-E-Styryl-2H-chromenes and 3-E-Styryl-2H-thiochromenes: Synthesis, Photophysical Studies, Anticancer Activity, and Exploration to Tricyclic Benzopyran Skeleton." ChemInform 46, no. 2 (December 19, 2014): no. http://dx.doi.org/10.1002/chin.201502138.
Повний текст джерелаSundaravelu, Nallappan, and Govindasamy Sekar. "Cu-Catalyzed one-pot synthesis of thiochromeno-quinolinone and thiochromeno-thioflavone via oxidative double hetero Michael addition using in situ generated nucleophiles." Chemical Communications 56, no. 62 (2020): 8826–29. http://dx.doi.org/10.1039/d0cc03210g.
Повний текст джерелаZhu, Yong-Ming, Fang-Ling Zhang, Zhen-Bang Chen, Kui Liu, Qing Yuan, and Qing Jiang. "Carbonylative Synthesis of Thiochromenones via Palladium-Catalyzed tert-Butyl Isocyanide Insertion." Synlett 29, no. 05 (January 23, 2018): 621–26. http://dx.doi.org/10.1055/s-0036-1591893.
Повний текст джерелаLe, Thi Thu Huong, Chitose Youhei, Quy Hien Le, Thanh Binh Nguyen та Dinh Hung Mac. "Convenient one-pot access to 2H-3-nitrothiochromenes from 2-bromobenzaldehydes, sodium sulfide and β-nitrostyrenes". Organic & Biomolecular Chemistry 17, № 26 (2019): 6355–58. http://dx.doi.org/10.1039/c9ob01060b.
Повний текст джерелаRam, Vishnu Ji, P. Srivastava, and Abhishek S. Saxena. "Carbanion-Induced Base-Catalyzed Synthesis of 1H-Isothiochromenes, Benzo[c]thiochromenes, Benzo[c]chromenes, and 1-Benzothiophenes through Ring-Transformation Reactions of 6-Aryl-2H-pyran-2-ones†." Journal of Organic Chemistry 66, no. 16 (August 2001): 5333–37. http://dx.doi.org/10.1021/jo0100648.
Повний текст джерелаMunshi, Parthapratim, and T. N. Guru Row. "2H-Thiochromene-2-thione." Acta Crystallographica Section E Structure Reports Online 60, no. 11 (October 30, 2004): o2168—o2170. http://dx.doi.org/10.1107/s1600536804026984.
Повний текст джерелаPeng, Jinsong, Chunxia Chen, Deqiang Wang, Peng Sun, Peiyun Jia, and Yixia Yue. "Transition-Metal-Free One-Pot Tandem Synthesis of 4-Quinolone and 4H-Thiochromen-4-one Derivatives Through Sequential Nucleophilic Addition–Elimination–SNAr Reaction." Synthesis 49, no. 18 (July 19, 2017): 4309–20. http://dx.doi.org/10.1055/s-0036-1588466.
Повний текст джерелаRam, Vishnu Ji, P. Srivastava, and Abhisbek S. Saxena. "ChemInform Abstract: Carbanion-Induced Base-Catalyzed Synthesis of 1H-Isothiochromenes, Benzo[c]thiochromenes, Benzo[c]chromenes, and 1-Benzothiophenes Through Ring-Transformation Reactions of 6-Aryl-2H-pyran-2-ones." ChemInform 32, no. 49 (May 23, 2010): no. http://dx.doi.org/10.1002/chin.200149097.
Повний текст джерелаWen, Li-Rong, Qiang-Yu Shen, Wei-Si Guo, and Ming Li. "Copper-catalyzed tandem arylation–cyclization of 2-alkynylaryl isothiocyanates with diaryliodonium salts: an efficient synthesis of thiochromeno[2,3-b]indoles." Organic Chemistry Frontiers 3, no. 7 (2016): 870–74. http://dx.doi.org/10.1039/c6qo00133e.
Повний текст джерелаSajadikhah, Seyed Sajad, and Mahmoud Nassiri. "Synthesis of 2H-thiochromene derivatives (microreview)." Chemistry of Heterocyclic Compounds 57, no. 11 (November 2021): 1073–75. http://dx.doi.org/10.1007/s10593-021-03026-x.
Повний текст джерелаLozynskyi, Andrii, Julia Senkiv, Iryna Ivasechko, Nataliya Finiuk, Olga Klyuchivska, Nataliya Kashchak, Danylo Lesyk, et al. "1,4-Naphthoquinone Motif in the Synthesis of New Thiopyrano[2,3-d]thiazoles as Potential Biologically Active Compounds." Molecules 27, no. 21 (November 4, 2022): 7575. http://dx.doi.org/10.3390/molecules27217575.
Повний текст джерелаMunshi, Parthapratim, and T. N. Guru Row. "2H-Thiochromen-2-one." Acta Crystallographica Section E Structure Reports Online 58, no. 4 (March 8, 2002): o353—o354. http://dx.doi.org/10.1107/s1600536802003628.
Повний текст джерелаSomasundaram, M., S. Athavan, K. K. Balasubramanian, R. Saiganesh, and S. Kabilan. "3-[(4-Oxo-4H-thiochromen-3-yl)methyl]-4H-thiochromen-4-one." Acta Crystallographica Section E Structure Reports Online 69, no. 3 (February 9, 2013): o358. http://dx.doi.org/10.1107/s1600536813001906.
Повний текст джерелаMahato, Karuna, Prasanta Ray Bagdi, and Abu T. Khan. "K2CO3 catalyzed regioselective synthesis of thieno[2,3-b]thiochromen-4-one oximes: access to the corresponding amine and nitroso derivatives." Organic & Biomolecular Chemistry 15, no. 26 (2017): 5625–34. http://dx.doi.org/10.1039/c7ob01033h.
Повний текст джерелаPandya, Dhananjay, and Yogesh Naliapara. "Synthesis and Anti Cervical Cancer Activity of Novel 5H-Thiochromeno [4,3-d]pyrimidines." Letters in Organic Chemistry 17, no. 4 (March 25, 2020): 294–302. http://dx.doi.org/10.2174/1570178616666190705152116.
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