Статті в журналах з теми "Sulfa-Michael"
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Tözendemir, Deniz, та Cihangir Tanyeli. "The synthesis of chiral β-naphthyl-β-sulfanyl ketones via enantioselective sulfa-Michael reaction in the presence of a bifunctional cinchona/sulfonamide organocatalyst". Beilstein Journal of Organic Chemistry 17 (18 лютого 2021): 494–503. http://dx.doi.org/10.3762/bjoc.17.43.
Повний текст джерелаEnders, Dieter, Karsten Lüttgen, and Arun Narine. "Asymmetric Sulfa-Michael Additions." Synthesis 2007, no. 7 (April 2007): 959–80. http://dx.doi.org/10.1055/s-2007-965968.
Повний текст джерелаCong, Zi-Song, Yang-Guo Li, Guang-Fen Du, Cheng-Zhi Gu, Bin Dai, and Lin He. "N-Heterocyclic carbene-catalyzed sulfa-Michael addition of enals." Chemical Communications 53, no. 98 (2017): 13129–32. http://dx.doi.org/10.1039/c7cc07269d.
Повний текст джерелаChen, Jiean, Sixuan Meng, Leming Wang, Hongmei Tang, and Yong Huang. "Highly enantioselective sulfa-Michael addition reactions using N-heterocyclic carbene as a non-covalent organocatalyst." Chemical Science 6, no. 7 (2015): 4184–89. http://dx.doi.org/10.1039/c5sc00878f.
Повний текст джерелаDeau, Emmanuel, Alexandra Le Foll, Clémence Fouache, Emilie Corrot, Laetitia Bailly, Vincent Levacher, Pierric Marchand, Florian Querniard, Laurent Bischoff та Jean-François Brière. "Organocatalytic enantioselective synthesis of β-amino sulfonic acid derivatives". Chemical Communications 57, № 67 (2021): 8348–51. http://dx.doi.org/10.1039/d1cc03477d.
Повний текст джерелаGui, Yong-Yuan, Jian Yang, Liang-Wen Qi, Xiao Wang, Fang Tian, Xiao-Nian Li, Lin Peng, and Li-Xin Wang. "A cinchona alkaloid catalyzed enantioselective sulfa-Michael/aldol cascade reaction of isoindigos: construction of chiral bispirooxindole tetrahydrothiophenes with vicinal quaternary spirocenters." Organic & Biomolecular Chemistry 13, no. 22 (2015): 6371–79. http://dx.doi.org/10.1039/c5ob00774g.
Повний текст джерелаQin, Tianyou, Lu Cheng, Sean Xiao-An Zhang, and Weiwei Liao. "Stereoselective synthesis of organosulfur compounds incorporating N-aromatic heterocyclic motifs and quaternary carbon centers via a sulfa-Michael triggered tandem reaction." Chemical Communications 51, no. 47 (2015): 9714–17. http://dx.doi.org/10.1039/c5cc01875g.
Повний текст джерелаFormica, Michele, Geoffroy Sorin, Alistair J. M. Farley, Jesús Díaz, Robert S. Paton, and Darren J. Dixon. "Bifunctional iminophosphorane catalysed enantioselective sulfa-Michael addition of alkyl thiols to alkenyl benzimidazoles." Chemical Science 9, no. 34 (2018): 6969–74. http://dx.doi.org/10.1039/c8sc01804a.
Повний текст джерелаChen, F. E., L. Dai, and S. X. Wang. "Cinchona Alkaloid Squaramide Catalyzed Sulfa-Michael Addition." Synfacts 2010, no. 11 (October 21, 2010): 1301. http://dx.doi.org/10.1055/s-0030-1258780.
Повний текст джерелаLi, Yuan-Zhen, Ying Wang, Guang-Fen Du, Hai-Yan Zhang, Hong-Li Yang, and Lin He. "N-Heterocyclic-Carbene-Catalyzed Sulfa-Michael additions." Asian Journal of Organic Chemistry 4, no. 4 (January 29, 2015): 327–32. http://dx.doi.org/10.1002/ajoc.201402241.
Повний текст джерелаQiu, Lin, Zhongqing Wen, Yuling Li, Kai Tian, Youchao Deng, Ben Shen, Yanwen Duan, and Yong Huang. "Stereoselective functionalization of platensimycin and platencin by sulfa-Michael/aldol reactions." Organic & Biomolecular Chemistry 17, no. 17 (2019): 4261–72. http://dx.doi.org/10.1039/c9ob00324j.
Повний текст джерелаYang, Lei, Jian-Qiang Zhao, Yong You, Zhen-Hua Wang, and Wei-Cheng Yuan. "Organocatalytic enantioselective tandem sulfa-Michael/aldol reaction to access dihydrothiopyran-fused benzosulfolane skeletons bearing three contiguous stereocenters." Chemical Communications 56, no. 82 (2020): 12363–66. http://dx.doi.org/10.1039/d0cc04840b.
Повний текст джерелаMeninno, Sara, Ilaria Quaratesi, Chiara Volpe, Andrea Mazzanti, and Alessandra Lattanzi. "Catalytic enantioselective one-pot approach tocis- andtrans-2,3-diaryl substituted 1,5-benzothiazepines." Organic & Biomolecular Chemistry 16, no. 38 (2018): 6923–34. http://dx.doi.org/10.1039/c8ob01988f.
Повний текст джерелаYang, Jinchao, Alistair J. M. Farley та Darren J. Dixon. "Enantioselective bifunctional iminophosphorane catalyzed sulfa-Michael addition of alkyl thiols to unactivated β-substituted-α,β-unsaturated esters". Chemical Science 8, № 1 (2017): 606–10. http://dx.doi.org/10.1039/c6sc02878k.
Повний текст джерелаWang, Weiying, Jiajun Wang, Shiye Li, Chaoping Li, Rong Tan, and Donghong Yin. "Iron(ii)-folded single-chain nanoparticles: a metalloenzyme mimicking sustainable catalyst for highly enantioselective sulfa-Michael addition in water." Green Chemistry 22, no. 14 (2020): 4645–55. http://dx.doi.org/10.1039/d0gc00949k.
Повний текст джерелаYang, Hui, Choon-Hong Tan, and Ming Wah Wong. "In silico characterization and prediction of thiourea-like neutral bidentate halogen bond catalysts." Organic & Biomolecular Chemistry 19, no. 32 (2021): 7051–60. http://dx.doi.org/10.1039/d1ob01092a.
Повний текст джерелаNagaraju, Sakkani, Neeli Satyanarayana, Banoth Paplal, Anuji K. Vasu, Sriram Kanvah, Balasubramanian Sridhar, Prabhakar Sripadi, and Dhurke Kashinath. "Correction: One-pot synthesis of functionalized isoxazole–thiolane hybrids via Knoevenagel condensation and domino sulfa-1,6-Michael/intramolecular vinylogous Henry reactions." RSC Advances 5, no. 124 (2015): 102399. http://dx.doi.org/10.1039/c5ra90105g.
Повний текст джерелаNagaraju, Sakkani, Neeli Satyanarayana, Banoth Paplal, Anuji K. Vasu, Sriram Kanvah, Balasubramanian Sridhar, Prabhakar Sripadi, and Dhurke Kashinath. "One-pot synthesis of functionalized isoxazole–thiolane hybrids via Knoevenagel condensation and domino sulfa-1,6-Michael/intramolecular vinylogous Henry reactions." RSC Advances 5, no. 114 (2015): 94474–78. http://dx.doi.org/10.1039/c5ra16721c.
Повний текст джерелаFulton, Jennifer L., Matthew A. Horwitz, Ericka L. Bruske, and Jeffrey S. Johnson. "Asymmetric Organocatalytic Sulfa-Michael Addition to Enone Diesters." Journal of Organic Chemistry 83, no. 6 (March 7, 2018): 3385–91. http://dx.doi.org/10.1021/acs.joc.8b00007.
Повний текст джерелаMeninno, Sara, Simone Naddeo, Luca Varricchio, Amedeo Capobianco та Alessandra Lattanzi. "Stereoselective organocatalytic sulfa-Michael reactions of aryl substituted α,β-unsaturated N-acyl pyrazoles". Organic Chemistry Frontiers 5, № 12 (2018): 1967–77. http://dx.doi.org/10.1039/c8qo00357b.
Повний текст джерелаZhu, Xiao-Yu, Mei-Heng Lv, Ya-Nan Zhao, Li-Yan Lan, Wen-Ze Li, and Lin-Jiu Xiao. "Organocatalytic sulfa-Michael/aldol cascade: constructing functionalized 2,5-dihydrothiophenes bearing a quaternary carbon stereocenter." RSC Advances 8, no. 59 (2018): 34000–34003. http://dx.doi.org/10.1039/c8ra04325f.
Повний текст джерелаLuna, Isadora Silva, Rayssa Marques Duarte da Cruz, Ryldene Marques Duarte da Cruz, Rodrigo Santos Aquino de Araújo, and Francisco Jaime Bezerra Mendonça-Junior. "1,4-Dithiane-2,5-diol: A Versatile Synthon for the Synthesis of Sulfur-containing Heterocycles." Current Organic Synthesis 15, no. 8 (December 17, 2018): 1026–42. http://dx.doi.org/10.2174/1570179415666180821154551.
Повний текст джерелаChen, J. R., W. J. Xiao, X. F. Wang, Q. L. Hua, Y. Cheng, X. L. An, and Q. Q. Yang. "Sulfa-Michael Reaction Cascade for the Synthesis of Chromans." Synfacts 2010, no. 12 (November 22, 2010): 1421. http://dx.doi.org/10.1055/s-0030-1258933.
Повний текст джерелаLi, Yuan-Zhen, Ying Wang, Guang-Fen Du, Hai-Yan Zhang, Hong-Li Yang, and Lin He. "ChemInform Abstract: N-Heterocyclic-Carbene-Catalyzed Sulfa-Michael Additions." ChemInform 46, no. 49 (November 19, 2015): no. http://dx.doi.org/10.1002/chin.201549069.
Повний текст джерелаYang, Yi, and Daming Du. "Enantioselective Construction of Functionalized Thiochromans via Squaramide-Catalyzed Asymmetric Cascade Sulfa-Michael/Michael Addition." Chinese Journal of Chemistry 32, no. 9 (August 25, 2014): 853–58. http://dx.doi.org/10.1002/cjoc.201400391.
Повний текст джерелаZhang, Shaowei, Demin Ren, Xiaolian Hu, Xingliang Fu, and Xiaofang Li. "Synthesis of Spiro Indazole-Tetrahydrothiophenes via Sulfa-Michael/Aldol Cascade Reactions." Journal of Chemical Research 41, no. 11 (November 2017): 641–44. http://dx.doi.org/10.3184/174751917x15094552081170.
Повний текст джерелаMomo, Patricia B., Eduardo F. Mizobuchi, Radell Echemendía, Isabel Baddeley, Matthew N. Grayson та Antonio C. B. Burtoloso. "Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones". Journal of Organic Chemistry 87, № 5 (18 лютого 2022): 3482–90. http://dx.doi.org/10.1021/acs.joc.1c03045.
Повний текст джерелаFulton, Jennifer L., Matthew A. Horwitz, Ericka L. Bruske, and Jeffrey S. Johnson. "Correction to Asymmetric Organocatalytic Sulfa-Michael Addition to Enone Diesters." Journal of Organic Chemistry 86, no. 1 (December 9, 2020): 1308. http://dx.doi.org/10.1021/acs.joc.0c02754.
Повний текст джерелаDong, Xiu-Qin, Xin Fang, and Chun-Jiang Wang. "Organocatalytic Asymmetric Sulfa-Michael Addition of Thiols to 4,4,4-Trifluorocrotonates." Organic Letters 13, no. 16 (August 19, 2011): 4426–29. http://dx.doi.org/10.1021/ol201766k.
Повний текст джерелаEnders, Dieter, та Krzysztof Hoffman. "Organocatalytic Asymmetric Sulfa-Michael Additions to α,β-Unsaturated Sulfonates". European Journal of Organic Chemistry 2009, № 11 (квітень 2009): 1665–68. http://dx.doi.org/10.1002/ejoc.200801202.
Повний текст джерелаRicci, Paolo, Armando Carlone, Giuseppe Bartoli, Marcella Bosco, Letizia Sambri та Paolo Melchiorre. "Organocatalytic Asymmetric Sulfa-Michael Addition to α,β-Unsaturated Ketones". Advanced Synthesis & Catalysis 350, № 1 (4 січня 2008): 49–53. http://dx.doi.org/10.1002/adsc.200700382.
Повний текст джерелаMeninno, Sara, Chiara Volpe, Giorgio Della Sala, Amedeo Capobianco, and Alessandra Lattanzi. "Stereoselective amine-thiourea-catalysed sulfa-Michael/nitroaldol cascade approach to 3,4,5-substituted tetrahydrothiophenes bearing a quaternary stereocenter." Beilstein Journal of Organic Chemistry 12 (April 5, 2016): 643–47. http://dx.doi.org/10.3762/bjoc.12.63.
Повний текст джерелаYan, Jinlong, Xinliang Fu, and Wei Li. "Synthesis of Spiro Thiazolo[3,2-a]Pyrimidine-Tetrahydrothiophenes via Sulfa-Michael/Aldol Cascade Reactions." Journal of Chemical Research 41, no. 12 (December 2017): 722–24. http://dx.doi.org/10.3184/174751917x15125690124282.
Повний текст джерелаDuan, Jindian, Jing Cheng, Bing Li, Fei Qi, and Pengfei Li. "Enantioselective Synthesis of Spiro[1,3-indanedione-tetrahydrothiophene]s by Organocatalytic Sulfa-Michael/Michael Domino Reaction." European Journal of Organic Chemistry 2015, no. 28 (September 1, 2015): 6130–34. http://dx.doi.org/10.1002/ejoc.201500837.
Повний текст джерелаLei, Jiaying, Xinliang Fu, Yulin Huang, and Xiaofang Li. "Synthesis of spiro[benzo[4,5]imidazo[2,1-b][1,3]thiazole-2,3-thiolane]s via sulfa-Michael/aldol cascade reactions." Journal of Chemical Research 43, no. 1-2 (January 2019): 63–66. http://dx.doi.org/10.1177/1747519819831898.
Повний текст джерелаLong, Xianwen, Min Zhang, Xiaodong Yang, and Jun Deng. "Total Synthesis of (±)-Spiroaxillarone A via a Reversible Sulfa-Michael Addition." Organic Letters 24, no. 6 (January 31, 2022): 1303–7. http://dx.doi.org/10.1021/acs.orglett.1c04282.
Повний текст джерелаLi, Zheng, Geyang Song, Jiaojiao He, Yan Du, and Jingya Yang. "Catalyst-free sulfa-Michael addition of pyrimidine-2-thiol to nitroolefins." Journal of Sulfur Chemistry 38, no. 6 (August 28, 2017): 686–98. http://dx.doi.org/10.1080/17415993.2017.1369541.
Повний текст джерелаLiang, Jian-Jun, Jin-Yun Pan, Dong-Cheng Xu, and Jian-Wu Xie. "Construction of polyheterocyclic spirotetrahydrothiophene derivatives via sulfa-Michael/aldol cascade reaction." Tetrahedron Letters 55, no. 46 (November 2014): 6335–38. http://dx.doi.org/10.1016/j.tetlet.2014.09.101.
Повний текст джерелаKlepp, Julian, Harald Podversnik, Johannes Puschnig, Andrew Wallace, and Ben W. Greatrex. "Diastereoselective sulfa-Michael reactions controlled by a biomass-derived chiral auxiliary." Tetrahedron 75, no. 29 (July 2019): 3894–903. http://dx.doi.org/10.1016/j.tet.2019.05.051.
Повний текст джерелаRana, Nirmal K., Sermadurai Selvakumar та Vinod K. Singh. "Highly Enantioselective Organocatalytic Sulfa-Michael Addition to α,β-Unsaturated Ketones". Journal of Organic Chemistry 75, № 6 (19 березня 2010): 2089–91. http://dx.doi.org/10.1021/jo902634a.
Повний текст джерелаFeng, Ze-Nan, Jin-Yun Luo, Yang Zhang, Guang-Fen Du, and Lin He. "N-Heterocyclic carbene-catalyzed diastereoselective synthesis of sulfenylated indanes via sulfa-Michael–Michael (aldol) cascade reactions." Organic & Biomolecular Chemistry 17, no. 19 (2019): 4700–4704. http://dx.doi.org/10.1039/c9ob00210c.
Повний текст джерелаYang, Yi, and Daming Du. "ChemInform Abstract: Enantioselective Construction of Functionalized Thiochromans via Squaramide-Catalyzed Asymmetric Cascade Sulfa-Michael/Michael Addition." ChemInform 46, no. 10 (February 19, 2015): no. http://dx.doi.org/10.1002/chin.201510027.
Повний текст джерелаKowalczyk, Rafał, Przemysław J. Boratyński, Aleksandra J. Wierzba, and Julia Bąkowicz. "Site and stereoselectivity in sulfa-Michael addition to equivocally activated conjugated dienes." RSC Advances 5, no. 82 (2015): 66681–86. http://dx.doi.org/10.1039/c5ra09631f.
Повний текст джерелаEnders, Dieter, Bertram Schmid, Nico Erdmann, and Gerhard Raabe. "Asymmetric Synthesis of Thiadecalins via an Organocatalytic Triple Cascade/Sulfa-Michael Sequence." Synthesis 2010, no. 13 (May 27, 2010): 2271–77. http://dx.doi.org/10.1055/s-0029-1218804.
Повний текст джерелаPei, Qing-Lan, Wen-Yong Han, Zhi-Jun Wu, Xiao-Mei Zhang та Wei-Cheng Yuan. "Organocatalytic diastereo- and enantioselective sulfa-Michael addition to α,β-disubstituted nitroalkenes". Tetrahedron 69, № 26 (липень 2013): 5367–73. http://dx.doi.org/10.1016/j.tet.2013.04.125.
Повний текст джерелаLi, Yi-Pan, Shou-Fei Zhu, and Qi-Lin Zhou. "Chiral Spiro Phosphoramide-Catalyzed Sulfa-Michael Addition/Enantioselective Protonation of Exocyclic Enones." Organic Letters 21, no. 23 (November 20, 2019): 9391–95. http://dx.doi.org/10.1021/acs.orglett.9b03615.
Повний текст джерелаBreman, Arjen C., Suze E. M. Telderman, Roy P. M. van Santen, Jamie I. Scott, Jan H. van Maarseveen, Steen Ingemann та Henk Hiemstra. "CinchonaAlkaloid Catalyzed Sulfa-Michael Addition Reactions Leading to Enantiopure β-Functionalized Cysteines". Journal of Organic Chemistry 80, № 21 (21 жовтня 2015): 10561–74. http://dx.doi.org/10.1021/acs.joc.5b01660.
Повний текст джерелаDong, Xiu-Qin, Xin Fang, and Chun-Jiang Wang. "ChemInform Abstract: Organocatalytic Asymmetric Sulfa-Michael Addition of Thiols to 4,4,4-Trifluorocrotonates." ChemInform 42, no. 52 (December 1, 2011): no. http://dx.doi.org/10.1002/chin.201152075.
Повний текст джерелаDuan, Jindian, Jing Cheng, Bing Li, Fei Qi, and Pengfei Li. "ChemInform Abstract: Enantioselective Synthesis of Spiro[1,3-indanedione-tetrahydrothiophene]s by Organocatalytic Sulfa-Michael/Michael Domino Reaction." ChemInform 47, no. 7 (January 2016): no. http://dx.doi.org/10.1002/chin.201607117.
Повний текст джерелаLaskova, Julia, Irina Kosenko, Ivan Ananyev, Marina Stogniy, Igor Sivaev, and Vladimir Bregadze. "“Free of Base” Sulfa-Michael Addition for Novel o-Carboranyl-DL-Cysteine Synthesis." Crystals 10, no. 12 (December 11, 2020): 1133. http://dx.doi.org/10.3390/cryst10121133.
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