Статті в журналах з теми "Ortho-quinone methides"
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Chambers, Jeffrey D., Jason Crawford, Haydn W. R. Williams, Claude Dufresne, John Scheigetz, Michael A. Bernstein, and Cheuk K. Lau. "Reactions of 2-phenyl-4H-1,3,2-benzodioxaborin, a stable ortho-quinone methide precursor." Canadian Journal of Chemistry 70, no. 6 (June 1, 1992): 1717–32. http://dx.doi.org/10.1139/v92-216.
Повний текст джерелаWan, Peter, Beverly Barker, Li Diao, Maike Fischer, Yijian Shi, and Cheng Yang. "1995 Merck Frosst Award Lecture Quinone methides: relevant intermediates in organic chemistry." Canadian Journal of Chemistry 74, no. 4 (April 1, 1996): 465–75. http://dx.doi.org/10.1139/v96-051.
Повний текст джерелаSpivey, Alan, Christian Nielsen, and Hossay Abas. "Stereoselective Reactions of ortho-Quinone Methide and ortho-Quinone Methide Imines and Their Utility in Natural Product Synthesis." Synthesis 50, no. 20 (August 14, 2018): 4008–18. http://dx.doi.org/10.1055/s-0037-1610241.
Повний текст джерелаHuang, Hong-Ming, Xu-Yan Wu, Bo-Rong Leng, Yi-Long Zhu, Xin-Chao Meng, Yu Hong, Bo Jiang, and De-Cai Wang. "Cu(ii)-Catalyzed formal [4 + 2] cycloaddition between quinone methides (QMs) and electron-poor 3-vinylindoles." Organic Chemistry Frontiers 7, no. 2 (2020): 414–19. http://dx.doi.org/10.1039/c9qo01343a.
Повний текст джерелаBai, Wen-Ju, Jonathan G. David, Zhen-Gao Feng, Marisa G. Weaver, Kun-Liang Wu, and Thomas R. R. Pettus. "The Domestication of ortho-Quinone Methides." Accounts of Chemical Research 47, no. 12 (December 3, 2014): 3655–64. http://dx.doi.org/10.1021/ar500330x.
Повний текст джерелаTanaka, Kenta, Yosuke Asada, and Yujiro Hoshino. "A new cycloaddition profile for ortho-quinone methides: photoredox-catalyzed [6+4] cycloadditions for synthesis of benzo[b]cyclopenta[e]oxepines." Chemical Communications 58, no. 15 (2022): 2476–79. http://dx.doi.org/10.1039/d1cc06332d.
Повний текст джерелаLiang, Dong, Li-Ping Tan, Wen-Jing Xiao, and Jia-Rong Chen. "Inverse-electron-demand [4+2] cycloaddition of photogenerated aza-ortho-quinone methides with 1,3,5-triazinanes: access to perfluoroalkylated tetrahydroquinazolines." Chemical Communications 56, no. 26 (2020): 3777–80. http://dx.doi.org/10.1039/d0cc00747a.
Повний текст джерелаMayer, Martin, Maik Pahl, Matthias Spanka, Max Grellmann, Marcel Sickert, Christoph Schneider, Knut R. Asmis, and Detlev Belder. "Unravelling the configuration of transient ortho-quinone methides by combining microfluidics with gas phase vibrational spectroscopy." Physical Chemistry Chemical Physics 22, no. 8 (2020): 4610–16. http://dx.doi.org/10.1039/c9cp06435d.
Повний текст джерелаXu, Jianfeng, Shiru Yuan, Jingyi Peng, Maozhong Miao, Zhengkai Chen, and Hongjun Ren. "Base-mediated diastereoselective [4 + 3] annulation of in situ generated ortho-quinone methides with C,N-cyclic azomethine imines." Organic & Biomolecular Chemistry 15, no. 36 (2017): 7513–17. http://dx.doi.org/10.1039/c7ob01783a.
Повний текст джерелаSaha, Satyajit, Santosh Kumar Alamsetti, and Christoph Schneider. "Chiral Brønsted acid-catalyzed Friedel–Crafts alkylation of electron-rich arenes with in situ-generated ortho-quinone methides: highly enantioselective synthesis of diarylindolylmethanes and triarylmethanes." Chemical Communications 51, no. 8 (2015): 1461–64. http://dx.doi.org/10.1039/c4cc08559k.
Повний текст джерелаChen, Renjie, Yu Liu, and Sunliang Cui. "1,4-Conjugate addition/esterification of ortho-quinone methides in a multicomponent reaction." Chemical Communications 54, no. 83 (2018): 11753–56. http://dx.doi.org/10.1039/c8cc07328g.
Повний текст джерелаGu, Xiu, Hao Yuan, Jun Jiang, Yi Wu, and Wen-Ju Bai. "Catalytic Asymmetric Hydrophosphination of ortho-Quinone Methides." Organic Letters 20, no. 22 (November 6, 2018): 7229–33. http://dx.doi.org/10.1021/acs.orglett.8b03158.
Повний текст джерелаAllen, Emily E., Calvin Zhu, James S. Panek, and Scott E. Schaus. "Multicomponent Condensation Reactions via ortho-Quinone Methides." Organic Letters 19, no. 7 (March 30, 2017): 1878–81. http://dx.doi.org/10.1021/acs.orglett.7b00647.
Повний текст джерелаWillis, Nicky J., and Christopher D. Bray. "ortho-Quinone Methides in Natural Product Synthesis." Chemistry - A European Journal 18, no. 30 (June 15, 2012): 9160–73. http://dx.doi.org/10.1002/chem.201200619.
Повний текст джерелаSingh, Maya Shankar, Anugula Nagaraju, Namrata Anand, and Sushobhan Chowdhury. "ortho-Quinone methide (o-QM): a highly reactive, ephemeral and versatile intermediate in organic synthesis." RSC Adv. 4, no. 99 (2014): 55924–59. http://dx.doi.org/10.1039/c4ra11444b.
Повний текст джерелаLian, Xiao-Lei, Alafate Adili, Bin Liu, Zhong-Lin Tao, and Zhi-Yong Han. "Enantioselective [4 + 1] cycloaddition of ortho-quinone methides and bromomalonates under phase-transfer catalysis." Organic & Biomolecular Chemistry 15, no. 17 (2017): 3670–73. http://dx.doi.org/10.1039/c7ob00484b.
Повний текст джерелаZhang, Ling, Xiaoyan Lin, Dayun Huang, Xue Liu, and Xiangmei Wu. "Recent Advances in Triarylmethane Synthesis." Synthesis 52, no. 16 (May 14, 2020): 2311–29. http://dx.doi.org/10.1055/s-0040-1707115.
Повний текст джерелаCheng, Yuyu, Zhiqiang Fang, Yanwen Jia, Zhongyue Lu, Wenjun Li, and Pengfei Li. "Organocatalytic enantioselective conjugate addition of 2-naphthols to ortho-hydroxyphenyl substituted para-quinone methides: access to unsymmetrical triarylmethanes." RSC Advances 9, no. 42 (2019): 24212–17. http://dx.doi.org/10.1039/c9ra04768a.
Повний текст джерелаLiu, Lina, Zhenbo Yuan, Rui Pan, Yuye Zeng, Aijun Lin, Hequan Yao, and Yue Huang. "1,6-Conjugated addition-mediated [4 + 1] annulation: an approach to 2,3-dihydrobenzofurans." Organic Chemistry Frontiers 5, no. 4 (2018): 623–28. http://dx.doi.org/10.1039/c7qo00846e.
Повний текст джерелаZhou, Fan, Ying Cheng, Xiao-Peng Liu, Jia-Rong Chen, and Wen-Jing Xiao. "A visible light photoredox catalyzed carbon radical-mediated generation of ortho-quinone methides for 2,3-dihydrobenzofuran synthesis." Chemical Communications 55, no. 21 (2019): 3117–20. http://dx.doi.org/10.1039/c9cc00727j.
Повний текст джерелаXia, Chao, Dong-Chao Wang, Gui-Rong Qu, and Hai-Ming Guo. "Palladium-catalyzed enantioselective [5 + 4] annulation of ortho-quinone methides and vinylethylene carbonates." Organic Chemistry Frontiers 7, no. 12 (2020): 1474–80. http://dx.doi.org/10.1039/d0qo00128g.
Повний текст джерелаGharui, Chandan, Shreya Singh, and Subhas Chandra Pan. "Chiral phosphoric acid catalyzed enantioselective annulation of acyclic enecarbamates to in situ-generated ortho-quinone methides." Organic & Biomolecular Chemistry 15, no. 35 (2017): 7272–76. http://dx.doi.org/10.1039/c7ob01766a.
Повний текст джерелаWang, Junwei, Xiang Pan, Quanjin Rong, Lei Zhao, Lin Zhao, Weichen Dai, Kun Zhao, and Lihong Hu. "One-pot synthesis of indoles and quinolinones from ortho-tosylaminophenyl-substituted para-quinone methides." RSC Advances 10, no. 55 (2020): 33455–60. http://dx.doi.org/10.1039/d0ra05497f.
Повний текст джерелаYou, Yong, Ting-Ting Li, Shu-Pei Yuan, Ke-Xin Xie, Zhen-Hua Wang, Jian-Qiang Zhao, Ming-Qiang Zhou, and Wei-Cheng Yuan. "Catalytic asymmetric [4+2] cycloaddition of 1-((2-aryl)vinyl)naphthalen-2-ols with in situ generated ortho-quinone methides for the synthesis of polysubstituted chromanes." Chemical Communications 56, no. 3 (2020): 439–42. http://dx.doi.org/10.1039/c9cc08316b.
Повний текст джерелаZhang, Song, Xiaojun Yu, Jianke Pan, Chunhui Jiang, Hongsu Zhang та Tianli Wang. "Asymmetric synthesis of spiro-structural 2,3-dihydrobenzofurans via the bifunctional phosphonium salt-promoted [4 + 1] cyclization of ortho-quinone methides with α-bromoketones". Organic Chemistry Frontiers 6, № 22 (2019): 3799–803. http://dx.doi.org/10.1039/c9qo01096c.
Повний текст джерелаTan, Qingfa, Han Yu, Yao Luo, Fenzhen Chang, Xiaohua Liu, Yuqiao Zhou, and Xiaoming Feng. "Asymmetric catalytic [4+3] cycloaddition of ortho-quinone methides with oxiranes." Chemical Communications 57, no. 24 (2021): 3018–21. http://dx.doi.org/10.1039/d1cc00262g.
Повний текст джерелаLei, Lu, Yu-Feng Liang, Cui Liang, Jiang-Ke Qin, Cheng-Xue Pan, Gui-Fa Su, and Dong-Liang Mo. "Copper(i)-catalyzed [4 + 2] cycloaddition of aza-ortho-quinone methides with bicyclic alkenes." Organic & Biomolecular Chemistry 19, no. 15 (2021): 3379–83. http://dx.doi.org/10.1039/d1ob00319d.
Повний текст джерелаFeng, Ziwen, Zhenbo Yuan, Xiaobin Zhao, Yue Huang, and Hequan Yao. "A [4 + 1] annulation of ortho-electrophile-substituted para-quinone methides for the synthesis of indanes and isoindolines." Organic Chemistry Frontiers 6, no. 20 (2019): 3535–39. http://dx.doi.org/10.1039/c9qo00977a.
Повний текст джерелаXu, Guangyang, Shengbiao Tang, Ying Shao, and Jiangtao Sun. "B(C6F5)3-Catalyzed formal (4+1)-annulation of ortho-quinone methides with diazoacetates: access to 2,3-dihydrobenzofurans." Chemical Communications 55, no. 62 (2019): 9096–99. http://dx.doi.org/10.1039/c9cc04863d.
Повний текст джерелаZhang, Lili, Xiao Zhou, Pengfei Li, Zhantao Liu, Yang Liu, Yong Sun та Wenjun Li. "Asymmetric synthesis of chromene skeletons via organocatalytic domino reactions of in situ generated ortho-quinone methide with malononitrile and β-functionalized ketone". RSC Advances 7, № 62 (2017): 39216–20. http://dx.doi.org/10.1039/c7ra08157j.
Повний текст джерелаDuan, Kang, Hongjin Shi, Lin-Xuan Wang, Shuai-Shuai Li, Lubin Xu, and Jian Xiao. "Hydride transfer enabled switchable dearomatization of indoles in the carbocyclic ring and the pyrrole ring." Organic Chemistry Frontiers 7, no. 17 (2020): 2511–17. http://dx.doi.org/10.1039/d0qo00658k.
Повний текст джерелаYu, Xuan, Wenjie Lan, Jiaqi Li, Hui Bai, Zhaohai Qin, and Bin Fu. "Enantioselective one-pot synthesis of 4H-chromene derivatives catalyzed by a chiral Ni(ii) complex." RSC Advances 10, no. 72 (2020): 44437–41. http://dx.doi.org/10.1039/d0ra08906k.
Повний текст джерелаMukhopadhyay, Soumendranath, Chandan Gharui, and Subhas Chandra Pan. "Applications of Bifunctional Organocatalysts on ortho ‐Quinone Methides." Asian Journal of Organic Chemistry 8, no. 11 (September 26, 2019): 1970–84. http://dx.doi.org/10.1002/ajoc.201900466.
Повний текст джерелаBai, Wen-Ju, Jonathan G. David, Zhen-Gao Feng, Marisa G. Weaver, Kun-Liang Wu, and Thomas R. R. Pettus. "ChemInform Abstract: The Domestication of ortho-Quinone Methides." ChemInform 46, no. 15 (March 26, 2015): no. http://dx.doi.org/10.1002/chin.201515346.
Повний текст джерелаJha, Babli K., Jaggaraju Prudhviraj, Prathama S. Mainkar, Nagender Punna, and Srivari Chandrasekhar. "Diastereoselective synthesis of CF3-dihydrobenzofurans by [4+1] annulation of in situ-generated CF3-o-quinone methides and sulfur ylides." RSC Advances 10, no. 63 (2020): 38588–91. http://dx.doi.org/10.1039/d0ra08289a.
Повний текст джерелаCarceller-Ferrer, Laura, Gonzalo Blay, José R. Pedro, and Carlos Vila. "Squaramide-Catalyzed Enantioselective Michael Addition of Pyrazol-3- ones to ortho-Quinone Methides." Letters in Organic Chemistry 17, no. 11 (November 29, 2020): 837–44. http://dx.doi.org/10.2174/1876402911666190806105543.
Повний текст джерелаBarta, Petra, Ferenc Fülöp, and István Szatmári. "Mannich base-connected syntheses mediated by ortho-quinone methides." Beilstein Journal of Organic Chemistry 14 (March 6, 2018): 560–75. http://dx.doi.org/10.3762/bjoc.14.43.
Повний текст джерелаOsipov, D. V., V. A. Osyanin, and Yu N. Klimochkin. "ortho-Quinone methides as key intermediates in cascade heterocyclizations." Russian Chemical Reviews 86, no. 7 (July 27, 2017): 625–87. http://dx.doi.org/10.1070/rcr4679.
Повний текст джерелаWillis, Nicky J., and Christopher D. Bray. "ChemInform Abstract: ortho-Quinone Methides in Natural Product Synthesis." ChemInform 43, no. 46 (October 18, 2012): no. http://dx.doi.org/10.1002/chin.201246243.
Повний текст джерелаAdili, Alafate, Zhong-Lin Tao, Dian-Feng Chen, and Zhi-Yong Han. "Quinine-catalyzed highly enantioselective cycloannulation of o-quinone methides with malononitrile." Organic & Biomolecular Chemistry 13, no. 8 (2015): 2247–50. http://dx.doi.org/10.1039/c4ob02602k.
Повний текст джерелаZhang, Lili, Yang Liu, Kun Liu, Zhantao Liu, Ningning He, and Wenjun Li. "Asymmetric synthesis of dihydrocoumarins via the organocatalytic hetero-Diels–Alder reaction of ortho-quinone methides." Org. Biomol. Chem. 15, no. 41 (2017): 8743–47. http://dx.doi.org/10.1039/c7ob02325a.
Повний текст джерелаLumb, Jean-Philip, Kevin C. Choong, and Dirk Trauner. "ortho-Quinone Methides frompara-Quinones: Total Synthesis of Rubioncolin B." Journal of the American Chemical Society 130, no. 29 (July 2008): 9230–31. http://dx.doi.org/10.1021/ja803498r.
Повний текст джерелаUyanik, Muhammet, Kohei Nishioka, Ryutaro Kondo, and Kazuaki Ishihara. "Chemoselective oxidative generation of ortho-quinone methides and tandem transformations." Nature Chemistry 12, no. 4 (March 23, 2020): 353–62. http://dx.doi.org/10.1038/s41557-020-0433-4.
Повний текст джерелаLewis, Robert S., Christopher J. Garza, Ann T. Dang, Te Kie A. Pedro, and William J. Chain. "Michael Additions of Highly Basic Enolates to ortho-Quinone Methides." Organic Letters 17, no. 9 (April 23, 2015): 2278–81. http://dx.doi.org/10.1021/acs.orglett.5b00972.
Повний текст джерелаIvanov, Konstantin L., Stanislav I. Bezzubov, Mikhail Ya Melnikov, and Ekaterina M. Budynina. "Donor–acceptor cyclopropanes as ortho-quinone methide equivalents in formal (4 + 2)-cycloaddition to alkenes." Organic & Biomolecular Chemistry 16, no. 21 (2018): 3897–909. http://dx.doi.org/10.1039/c8ob00377g.
Повний текст джерелаZhang, Yueteng, Peng Ji, Xiang Meng, Feng Gao, Fanxun Zeng, and Wei Wang. "Facile Synthesis of 2H-Benzo[h]Chromenes via an Arylamine-Catalyzed Mannich Cyclization Cascade Reaction." Molecules 26, no. 12 (June 12, 2021): 3617. http://dx.doi.org/10.3390/molecules26123617.
Повний текст джерелаZhou, Ji, Mao-Lin Wang, Xiang Gao, Guo-Fang Jiang, and Yong-Gui Zhou. "Bifunctional squaramide-catalyzed synthesis of chiral dihydrocoumarins via ortho-quinone methides generated from 2-(1-tosylalkyl)phenols." Chemical Communications 53, no. 25 (2017): 3531–34. http://dx.doi.org/10.1039/c7cc01072a.
Повний текст джерелаHoshino, Yujiro, Kiyoshi Honda, Kenta Tanaka, Ko Ueno, Yuta Tanaka, Naoya Ohtsuka, Yosuke Asada, Mami Kishimoto, and Shuto Sunaga. "Dual In Situ Generation of Aliphatic Vinyl Ethers and Electron-Deficient ortho-Quinone Methides for Inverse-Electron-Demand [4+2] Cycloaddition: A Selective One-Pot Synthesis of 3-Alkylchromanes." Synlett 31, no. 12 (May 6, 2020): 1197–200. http://dx.doi.org/10.1055/s-0040-1707522.
Повний текст джерелаLiu, Si-Jia, Man-Su Tu, Kai-Yue Liu, Jia-Yi Chen, Shao-Fei Ni, Yu-Chen Zhang, and Feng Shi. "Organocatalytic Asymmetric [2 + 4] Cycloadditions of 3-Vinylindoles with ortho-Quinone Methides." Molecules 26, no. 21 (November 8, 2021): 6751. http://dx.doi.org/10.3390/molecules26216751.
Повний текст джерелаRen, Hongjun, Manman Sun, Jinyu Song, Lei Wang, Wenguang Yin, and Maozhong Miao. "Direct Propargylation of ortho-Quinone Methides with Alkynyl Zinc Reagents: An Application to the One-Pot Synthesis of 2,3-Disubstituted Benzofurans." Synlett 31, no. 08 (February 26, 2020): 818–22. http://dx.doi.org/10.1055/s-0039-1691739.
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