Статті в журналах з теми "Alkoxylation"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Alkoxylation".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Liu, Zhuqing, Fei Huang, Jiang Lou, Quannan Wang, and Zhengkun Yu. "Copper-promoted direct C–H alkoxylation of S,S-functionalized internal olefins with alcohols." Organic & Biomolecular Chemistry 15, no. 26 (2017): 5535–40. http://dx.doi.org/10.1039/c7ob01234a.
Повний текст джерелаShen, Jiabin, Jun Xu, Heng Cai, Chao Shen, and Pengfei Zhang. "Platinum(ii)-catalyzed selective para C–H alkoxylation of arylamines through a coordinating activation strategy." Organic & Biomolecular Chemistry 17, no. 3 (2019): 490–97. http://dx.doi.org/10.1039/c8ob02942c.
Повний текст джерелаLin, John, Upali Weerasooriya, E. Leach Bruce, Steve V. Orsak, and Park T. X. Cedar. "5627121 Process for preparing alkoxylation catalysts and alkoxylation process." Journal of Molecular Catalysis A: Chemical 125, no. 2-3 (November 1997): 182. http://dx.doi.org/10.1016/s1381-1169(98)80116-7.
Повний текст джерелаLiu, Lunzu, Guowei Li, and Mingzhi Huang. "ALKOXYLATION OF HYDRIDOPHOSPHORANES." Phosphorus, Sulfur, and Silicon and the Related Elements 69, no. 1-2 (June 1992): 1–6. http://dx.doi.org/10.1080/10426509208036849.
Повний текст джерелаWeerasooriya, Upali. "Ester alkoxylation technology." Journal of Surfactants and Detergents 2, no. 3 (July 1999): 373–81. http://dx.doi.org/10.1007/s11743-999-0092-5.
Повний текст джерелаLakhtin, V. G., V. L. Ryabkov, M. V. Polyakova, V. M. Nosova, A. F. Kisin, and E. A. Chernyshev. "Alkoxylation ofC-chlorovinylsilanes." Russian Chemical Bulletin 44, no. 4 (April 1995): 718–23. http://dx.doi.org/10.1007/bf00698510.
Повний текст джерелаRogers, R. L., and K. Hermann. "Upgrading an Alkoxylation Facility." Process Safety and Environmental Protection 82, no. 1 (January 2004): 12–17. http://dx.doi.org/10.1205/095758204322777624.
Повний текст джерелаRomanova, S. M., A. M. Madyakina, L. A. Fatykhova, and S. V. Fridland. "Alkoxylation of cellulose nitrates." Russian Journal of General Chemistry 83, no. 1 (January 2013): 58–62. http://dx.doi.org/10.1134/s1070363213010106.
Повний текст джерелаZhang, Yu-Feng, and Mohamed Mellah. "Samarium(ii)-electrocatalyzed chemoselective reductive alkoxylation of phthalimides." Organic Chemistry Frontiers 9, no. 5 (2022): 1308–14. http://dx.doi.org/10.1039/d1qo01760h.
Повний текст джерелаTakemura, Noriaki, Yoichiro Kuninobu, and Motomu Kanai. "Copper-catalyzed benzylic C(sp3)–H alkoxylation of heterocyclic compounds." Org. Biomol. Chem. 12, no. 16 (2014): 2528–32. http://dx.doi.org/10.1039/c4ob00215f.
Повний текст джерелаYamaguchi, Eiji, Nao Taguchi, and Akichika Itoh. "Ruthenium polypyridyl complex-catalysed aryl alkoxylation of styrenes: improving reactivity using a continuous flow photo-microreactor." Reaction Chemistry & Engineering 4, no. 6 (2019): 995–99. http://dx.doi.org/10.1039/c9re00061e.
Повний текст джерелаLi, Long, Xin-Qi Zhu, Ying-Qi Zhang, Hao-Zhen Bu, Peng Yuan, Jinyu Chen, Jingyi Su, Xianming Deng, and Long-Wu Ye. "Metal-free alkene carbooxygenation following tandem intramolecular alkoxylation/Claisen rearrangement: stereocontrolled access to bridged [4.2.1] lactones." Chemical Science 10, no. 10 (2019): 3123–29. http://dx.doi.org/10.1039/c9sc00079h.
Повний текст джерелаFan, Huaqiang, Yi Wan, Peng Pan, Wenbin Cai, Shihui Liu, Chuanxu Liu, and Yongqiang Zhang. "A cascade approach to 3D cyclic carbamates via an ionic decarboxylative functionalization of olefinic oxamic acids." Chemical Communications 56, no. 1 (2020): 86–89. http://dx.doi.org/10.1039/c9cc07709j.
Повний текст джерелаLu, Wenkui, Hui Xu, and Zengming Shen. "Copper-catalyzed aromatic C–H alkoxylation with alcohols under aerobic conditions." Organic & Biomolecular Chemistry 15, no. 5 (2017): 1261–67. http://dx.doi.org/10.1039/c6ob02582j.
Повний текст джерелаLiu, Yongxiang, Jia Guo, Yang Liu, Xiaoyu Wang, Yanshi Wang, Xinyu Jia, Gaofei Wei, Lizhu Chen, Jianyong Xiao, and Maosheng Cheng. "Au(i)-catalyzed triple bond alkoxylation/dienolether aromaticity-driven cascade cyclization to naphthalenes." Chem. Commun. 50, no. 47 (2014): 6243–45. http://dx.doi.org/10.1039/c4cc00464g.
Повний текст джерелаGatto, Mattia, Walter Baratta, Paola Belanzoni, Leonardo Belpassi, Alessandro Del Zotto, Francesco Tarantelli, and Daniele Zuccaccia. "Hydration and alkoxylation of alkynes catalyzed by NHC–Au–OTf." Green Chemistry 20, no. 9 (2018): 2125–34. http://dx.doi.org/10.1039/c8gc00508g.
Повний текст джерелаEnthaler, Stephan, and Anna Company. "Palladium-catalysed hydroxylation and alkoxylation." Chemical Society Reviews 40, no. 10 (2011): 4912. http://dx.doi.org/10.1039/c1cs15085e.
Повний текст джерелаHlavatý, Jaromír. "Anodic alkoxylation of N-phenylsulfonylpyrrole." Electrochimica Acta 40, no. 5 (April 1995): 625–28. http://dx.doi.org/10.1016/0013-4686(94)00336-y.
Повний текст джерелаKhutorianskyi, Viktor V., Norbert Baris, and Petr Beier. "Oxidative nucleophilic alkoxylation of nitrobenzenes." Organic Chemistry Frontiers 8, no. 1 (2021): 77–81. http://dx.doi.org/10.1039/d0qo01291b.
Повний текст джерелаLIU, L., G. LI, and M. HUANG. "ChemInform Abstract: Alkoxylation of Hydridophosphoranes." ChemInform 23, no. 42 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199242209.
Повний текст джерелаZhang, Shuaizhong, Jinquan Zhang, and Hongbin Zou. "C(sp3)–H oxygenation via alkoxypalladium(ii) species: an update for the mechanism." Chemical Science 13, no. 5 (2022): 1298–306. http://dx.doi.org/10.1039/d1sc06907a.
Повний текст джерелаZeng, Wanting, Moldir Nukeyeva, Qiumei Wang та Chao Jiang. "Synthesis of unnatural α-amino acid derivatives via selective o-C–H functionalization". Organic & Biomolecular Chemistry 16, № 4 (2018): 598–608. http://dx.doi.org/10.1039/c7ob02921g.
Повний текст джерелаXu, Zhaoliang, Yu Hu, Lei Wang, Mingli Sun, and Pinhua Li. "Merging cobalt and photoredox catalysis for the C8–H alkoxylation of 1-naphthylamine derivatives with alcohols." Organic & Biomolecular Chemistry 19, no. 46 (2021): 10112–19. http://dx.doi.org/10.1039/d1ob01721g.
Повний текст джерелаWang, Wei, Jun-Rong Song, Zhi-Yao Li, Ting Zhong, Qin Chi, Hai Ren, and Wei-Dong Pan. "Copper-catalyzed aerobic oxidative radical alkoxycyclization of tryptamines to access 3-alkoxypyrroloindolines." RSC Advances 11, no. 29 (2021): 18080–83. http://dx.doi.org/10.1039/d1ra02679h.
Повний текст джерелаTran, Chau B., Xuan N. T. Duong, Huy D. Lu, Thu T. V. Cao, and Thanh Truong. "Auxiliary-directed etherification of sp2 C–H bonds under heterogeneous metal–organic framework catalysis: synthesis of ethenzamide." RSC Advances 8, no. 5 (2018): 2829–36. http://dx.doi.org/10.1039/c7ra12010a.
Повний текст джерелаBeng, Timothy K., Victoria Shearer, Rachel Davey, and Ivianne Redman. "Site-selective, catalytic, and diastereoselective sp3 C–H hydroxylation and alkoxylation of vicinally functionalized lactams." RSC Advances 10, no. 34 (2020): 20264–71. http://dx.doi.org/10.1039/d0ra03726e.
Повний текст джерелаVilluendas, Pedro, Elena Serrano, and Esteban P. Urriolabeitia. "Pd-catalysed ortho-alkoxylation of benzamides N-protected with an iminophosphorane functionality." New Journal of Chemistry 39, no. 4 (2015): 3077–83. http://dx.doi.org/10.1039/c5nj00189g.
Повний текст джерелаBeng, Timothy K., Megan Bauder, Morgan J. Rodriguez, and Antonio Moreno. "Copper-catalyzed regioselective dehydrogenative alkoxylation of morpholinonyl alkenols: application to the synthesis of spirotricyclic dihydropyrans and of trans-fused bicyclic morpholines." New Journal of Chemistry 42, no. 20 (2018): 16451–55. http://dx.doi.org/10.1039/c8nj03890b.
Повний текст джерелаDong, Min, Yuqi Jia, Wei Zhou, Jinlai Gao, Xiaoqing Lv, Fan Luo, Yongqiang Zhang, and Shihui Liu. "A photoredox/nickel dual-catalytic strategy for benzylic C–H alkoxylation." Organic Chemistry Frontiers 8, no. 24 (2021): 6881–87. http://dx.doi.org/10.1039/d1qo01421h.
Повний текст джерелаIvandini, Tribidasari A., and Yasuaki Einaga. "Polycrystalline boron-doped diamond electrodes for electrocatalytic and electrosynthetic applications." Chemical Communications 53, no. 8 (2017): 1338–47. http://dx.doi.org/10.1039/c6cc08681k.
Повний текст джерелаZhang, Ying-Qi, Xin-Qi Zhu, Yin Xu, Hao-Zhen Bu, Jia-Le Wang, Tong-Yi Zhai, Jin-Mei Zhou, and Long-Wu Ye. "Synthesis of functionalized 3-isochromanones via metal-free intramolecular alkoxylation-initiated cascade cyclization." Green Chemistry 21, no. 11 (2019): 3023–28. http://dx.doi.org/10.1039/c9gc01030k.
Повний текст джерелаLi, Heng, Fan Lv, Xing Guo, Qinghua Wu, Hao Wu, Bing Tang, Changjiang Yu, Hua Wang, Lijuan Jiao, and Erhong Hao. "Direct C–H alkoxylation of BODIPY dyes via cation radical accelerated oxidative nucleophilic hydrogen substitution: a new route to building blocks for functionalized BODIPYs." Chemical Communications 57, no. 13 (2021): 1647–50. http://dx.doi.org/10.1039/d0cc07961h.
Повний текст джерелаShao, Zhong, Fang Wang, Jingqi Shi, Lifang Ma, and Ziyuan Li. "Synergetic copper/TEMPO-catalysed benzylic C–H imidation with N-fluorobenzenesulfonimide at room temperature and tandem conversions with alcohols or arenes." Organic Chemistry Frontiers 8, no. 13 (2021): 3298–307. http://dx.doi.org/10.1039/d1qo00340b.
Повний текст джерелаHao, Feiyue, Haruyasu Asahara, and Nagatoshi Nishiwaki. "A direct and vicinal functionalization of the 1-methyl-2-quinolone framework: 4-alkoxylation and 3-chlorination." Organic & Biomolecular Chemistry 14, no. 22 (2016): 5128–35. http://dx.doi.org/10.1039/c6ob00868b.
Повний текст джерелаSarkar, Souvik, Tapan Sahoo, Chiranjit Sen, and Subhash Chandra Ghosh. "Copper(ii) mediated ortho C–H alkoxylation of aromatic amines using organic peroxides: efficient synthesis of hindered ethers." Chemical Communications 57, no. 71 (2021): 8949–52. http://dx.doi.org/10.1039/d1cc01803e.
Повний текст джерелаPetrov, Vladimir F. "Alkoxylation in achiral calamitic liquid crystals." Liquid Crystals 29, no. 6 (June 1, 2002): 805–35. http://dx.doi.org/10.1080/02678290210133114.
Повний текст джерелаHou, Hong, Hengxue Li, Yue Xu, Daliang Tang, Ying Han, Chaoguo Yan, Xiaoyun Chen, and Shaoqun Zhu. "Catalyst-free fluorinative alkoxylation of alkenes." Tetrahedron 74, no. 45 (November 2018): 6577–83. http://dx.doi.org/10.1016/j.tet.2018.09.038.
Повний текст джерелаRose-Munch, Françsoise, Jean Pierre Djukic, and Eric Rose. "Hydro-de-alkoxylation of alkoxybenzenetricarbonylchromium complexes." Tetrahedron Letters 31, no. 18 (January 1990): 2589–90. http://dx.doi.org/10.1016/0040-4039(90)80132-6.
Повний текст джерелаIshida, Akito, Tatsumi Uesugi, and Setsuo Takamuku. "Photoinduced Alkoxylation of 2-Vinylpyridinium Ion." Bulletin of the Chemical Society of Japan 66, no. 5 (May 1993): 1580–82. http://dx.doi.org/10.1246/bcsj.66.1580.
Повний текст джерелаGuo, Ya-Fei, Bao-Hua Xu, Ting Li, Lei Wang, and Suo-Jiang Zhang. "Cobalt(ii)-catalyzed oxidative esterification of aldehydes: a cooperative effect between cobalt and iodide ions." Organic Chemistry Frontiers 3, no. 1 (2016): 47–52. http://dx.doi.org/10.1039/c5qo00293a.
Повний текст джерелаYang, Xinglin, Gang Shan, Zimo Yang, Guiyi Huang, Guoqiang Dong, Chunquan Sheng, and Yu Rao. "One-pot synthesis of quaternary carbon centered cyclobutanes via Pd(ii)-catalyzed cascade C(sp3)–H activations." Chemical Communications 53, no. 9 (2017): 1534–37. http://dx.doi.org/10.1039/c6cc06897a.
Повний текст джерелаAmri, Nasser, Ryan A. Skilton, Duncan Guthrie, and Thomas Wirth. "Efficient Flow Electrochemical Alkoxylation of Pyrrolidine-1-carbaldehyde." Synlett 30, no. 10 (March 26, 2019): 1183–86. http://dx.doi.org/10.1055/s-0037-1611774.
Повний текст джерелаYang, Can, Zhipeng Liu, Xinwei Hu, Haisheng Xie, Huanfeng Jiang та Wei Zeng. "Rh(iii)-Catalyzed Csp2–Csp3 bond alkoxylation of α-indolyl alcohols via C–C σ bond cleavage". Organic Chemistry Frontiers 8, № 12 (2021): 2949–54. http://dx.doi.org/10.1039/d1qo00194a.
Повний текст джерелаEstruch-Blasco, Manel, Irene Bosque, David Guijarro, and Jose C. Gonzalez-Gomez. "Electrochemically site-selective alkoxylation of twisted 2-arylbenzoic acids via spirolactonization." Organic Chemistry Frontiers 8, no. 18 (2021): 5130–38. http://dx.doi.org/10.1039/d1qo00834j.
Повний текст джерелаZhang, Jingran, Ayesha Jalil, Jiaxin He, Zhenyang Yu, Yifu Cheng, Guangchen Li, Yunfei Du, and Kang Zhao. "Lactonization with concomitant 1,2-aryl migration and alkoxylation mediated by dialkoxyphenyl iodides generated in situ." Chemical Communications 57, no. 60 (2021): 7426–29. http://dx.doi.org/10.1039/d1cc03110d.
Повний текст джерелаAbdolalian, Payam, Samaneh K. Tizhoush, Kaveh Farshadfar, and Alireza Ariafard. "The role of hypervalent iodine(iii) reagents in promoting alkoxylation of unactivated C(sp3)–H bonds catalyzed by palladium(ii) complexes." Chemical Science 12, no. 20 (2021): 7185–95. http://dx.doi.org/10.1039/d1sc01230d.
Повний текст джерелаMusik, Marlena, Marcin Bartkowiak, and Eugeniusz Milchert. "Advanced Methods for Hydroxylation of Vegetable Oils, Unsaturated Fatty Acids and Their Alkyl Esters." Coatings 12, no. 1 (December 23, 2021): 13. http://dx.doi.org/10.3390/coatings12010013.
Повний текст джерелаZhu, Jingshuai, Yiqun Xiao, Changxi Zhang, Boyu Jia, Heng Lu, Jiayu Wang, Xinhui Lu, Zhen Li, and Xiaowei Zhan. "Effects of alkoxylation position on fused-ring electron acceptors." Journal of Materials Chemistry C 8, no. 43 (2020): 15128–34. http://dx.doi.org/10.1039/d0tc02158j.
Повний текст джерелаHamana, Masatomo, Mitsuo Hayashida, and Haruyoshi Honda. "Deoxygenative 2-Alkoxylation of Quinoline 1-Oxide." HETEROCYCLES 31, no. 7 (1990): 1325. http://dx.doi.org/10.3987/com-90-5413.
Повний текст джерелаKidwai, Mazaahir, Parven Kumar, and Seema Kohli. "Microwave-induced Selective Alkoxylation of 1,4-Naphthoquinones†." Journal of Chemical Research, no. 1 (1997): 24–25. http://dx.doi.org/10.1039/a601810f.
Повний текст джерела