Статті в журналах з теми "Regioselective Hydroboration"
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Huang, Jiuzhong, Wuxin Yan, Chaowei Tan, Wanqing Wu, and Huanfeng Jiang. "Palladium-catalyzed regioselective hydroboration of aryl alkenes with B2pin2." Chemical Communications 54, no. 14 (2018): 1770–73. http://dx.doi.org/10.1039/c7cc09432a.
Повний текст джерелаLiu, Tianwei, Jianghua He, and Yuetao Zhang. "Regioselective 1,2-hydroboration of N-heteroarenes using a potassium-based catalyst." Organic Chemistry Frontiers 6, no. 15 (2019): 2749–55. http://dx.doi.org/10.1039/c9qo00497a.
Повний текст джерелаNichols, Brian R., Novruz G. Akhmedov, Jeffrey L. Petersen, and Brian V. Popp. "Access to a pair of ambiphilic phosphine–borane regioisomers by rhodium-catalyzed hydroboration." Dalton Transactions 47, no. 25 (2018): 8456–65. http://dx.doi.org/10.1039/c8dt01467a.
Повний текст джерелаThomas, Stephen, Nate Ang, Cornelia Buettner, Scott Docherty, Alessandro Bismuto, Jonathan Carney, Jamie Docherty, and Michael Cowley. "Borane-Catalysed Hydroboration of Alkynes and Alkenes." Synthesis 50, no. 04 (November 20, 2017): 803–8. http://dx.doi.org/10.1055/s-0036-1591719.
Повний текст джерелаReichardt, Bastian, Olaf R. Ludek, and Chris Meier. "New and Efficient Synthesis of Racemic Cyclopent-3-en-1-yl Nucleoside Analogues and Their Derivatives." Collection of Czechoslovak Chemical Communications 71, no. 7 (2006): 1011–28. http://dx.doi.org/10.1135/cccc20061011.
Повний текст джерелаZhao, Jie, Zhiqiang Niu, Hua Fu, and Yadong Li. "Ligand-free hydroboration of alkynes catalyzed by heterogeneous copper powder with high efficiency." Chem. Commun. 50, no. 16 (2014): 2058–60. http://dx.doi.org/10.1039/c3cc48670b.
Повний текст джерелаYang, Ying, Jia-Hao Zeng, and Zhuang-Ping Zhan. "Regio-divergent hydroboration of terminal allenes controlled by nickel and cobalt catalysts." Organic Chemistry Frontiers 8, no. 11 (2021): 2537–42. http://dx.doi.org/10.1039/d1qo00024a.
Повний текст джерелаKeyzer, Evan N., Sky S. Kang, Schirin Hanf, and Dominic S. Wright. "Regioselective 1,4-hydroboration of pyridines catalyzed by an acid-initiated boronium cation." Chemical Communications 53, no. 68 (2017): 9434–37. http://dx.doi.org/10.1039/c7cc04988a.
Повний текст джерелаCao, Xu, Jia Li, Anqiao Zhu, Fan Su, Weiwei Yao, Fei Xue, and Mengtao Ma. "Syntheses of asymmetrical magnesium(i) complexes and their catalytic application in epoxide hydroboration." Organic Chemistry Frontiers 7, no. 22 (2020): 3625–32. http://dx.doi.org/10.1039/d0qo00938e.
Повний текст джерелаBaldassari, Lucas L., Kelvin S. Santos, Camila P. Ebersol, Diogo S. Lüdtke, and Angélica V. Moro. "Ligand-free, catalytic and regioselective hydroboration of selenoalkynes." Catalysis Science & Technology 10, no. 22 (2020): 7476–80. http://dx.doi.org/10.1039/d0cy01379j.
Повний текст джерелаTai, Chia-Cheng, Ming-Shiuan Yu, Yi-Lin Chen, Wen-Hang Chuang, Ting-Hua Lin, Glenn P. A. Yap, and Tiow-Gan Ong. "Synthesis of a guanidine NHC complex and its application in borylation reactions." Chem. Commun. 50, no. 33 (2014): 4344–46. http://dx.doi.org/10.1039/c4cc00550c.
Повний текст джерелаFan, Xiaoting, Junhao Zheng, Zhen Hua Li, and Huadong Wang. "Organoborane Catalyzed Regioselective 1,4-Hydroboration of Pyridines." Journal of the American Chemical Society 137, no. 15 (April 10, 2015): 4916–19. http://dx.doi.org/10.1021/jacs.5b03147.
Повний текст джерелаKaithal, Akash, Basujit Chatterjee, and Chidambaram Gunanathan. "Ruthenium-Catalyzed Regioselective 1,4-Hydroboration of Pyridines." Organic Letters 18, no. 14 (June 28, 2016): 3402–5. http://dx.doi.org/10.1021/acs.orglett.6b01564.
Повний текст джерелаZhang, Guoqi, Jing Wu, Man Wang, Haisu Zeng, Jessica Cheng, Michelle C. Neary, and Shengping Zheng. "Cobalt-Catalyzed Regioselective Hydroboration of Terminal Alkenes." European Journal of Organic Chemistry 2017, no. 38 (October 16, 2017): 5814–18. http://dx.doi.org/10.1002/ejoc.201701047.
Повний текст джерелаYoshida, Hiroto, Ikuo Kageyuki, and Ken Takaki. "Silver-Catalyzed Highly Regioselective Formal Hydroboration of Alkynes." Organic Letters 16, no. 13 (June 13, 2014): 3512–15. http://dx.doi.org/10.1021/ol501465x.
Повний текст джерелаEndo, Kohei, Munenao Hirokami, and Takanori Shibata. "Counteranion-Accelerated RhIOAc-Catalyzed Regioselective Hydroboration of Vinylarenes." Organometallics 27, no. 20 (October 27, 2008): 5390–93. http://dx.doi.org/10.1021/om800465q.
Повний текст джерелаTamang, Sem Raj, Arpita Singh, Daniel K. Unruh, and Michael Findlater. "Nickel-Catalyzed Regioselective 1,4-Hydroboration of N-Heteroarenes." ACS Catalysis 8, no. 7 (June 4, 2018): 6186–91. http://dx.doi.org/10.1021/acscatal.8b01166.
Повний текст джерелаHuang, Yun-Shuai, Jie Wang, Wan-Xin Zheng, Feng-Lian Zhang, You-Jie Yu, Min Zheng, Xiaoguo Zhou та Yi-Feng Wang. "Regioselective radical hydroboration of electron-deficient alkenes: synthesis of α-boryl functionalized molecules". Chemical Communications 55, № 79 (2019): 11904–7. http://dx.doi.org/10.1039/c9cc06506g.
Повний текст джерелаMandal, Souvik, Piyush Kumar Verma, and K. Geetharani. "Lewis acid catalysis: regioselective hydroboration of alkynes and alkenes promoted by scandium triflate." Chemical Communications 54, no. 97 (2018): 13690–93. http://dx.doi.org/10.1039/c8cc08361d.
Повний текст джерелаLiu, Yuhua, ZhongJie Jiang, and Jipei Chen. "Origin of the ligand effect in the cobalt catalyzed regioselective hydroboration of 1,3-diene." Organic & Biomolecular Chemistry 18, no. 19 (2020): 3747–53. http://dx.doi.org/10.1039/d0ob00628a.
Повний текст джерелаŠkoch, Karel, Constantin G. Daniliuc, Gerald Kehr, and Gerhard Erker. "Using the FpXylBH2•SMe2 reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes." Chemical Communications 56, no. 81 (2020): 12178–81. http://dx.doi.org/10.1039/d0cc05230b.
Повний текст джерелаNarasimhan, S., K. Ganeshwar Prasad, and S. Madhavan. "Remarkable regioselective hydroboration of terminal alkenes by calcium borohydride." Tetrahedron Letters 36, no. 7 (February 1995): 1141–44. http://dx.doi.org/10.1016/0040-4039(94)02441-d.
Повний текст джерелаFan, Xiaoting, Junhao Zheng, Zhen Hua Li, and Huadong Wang. "ChemInform Abstract: Organoborane Catalyzed Regioselective 1,4-Hydroboration of Pyridines." ChemInform 46, no. 41 (September 24, 2015): no. http://dx.doi.org/10.1002/chin.201541209.
Повний текст джерелаOliveira, Isadora M., Henrique A. Esteves, Mariana P. Darbem, Arthur Sartorelli, Thiago C. Correra, André F. Rodrigues‐Oliveira, Daniel C. Pimenta, Julio Zukerman‐Schpector, Flávia Manarin, and Hélio A. Stefani. "Stereo‐ and Regioselective Cu‐Catalyzed Hydroboration of Alkynyl Chalcogenoethers." ChemCatChem 12, no. 13 (May 25, 2020): 3545–52. http://dx.doi.org/10.1002/cctc.202000395.
Повний текст джерелаRamachandran, P. Veeraraghavan, Sateesh Madhi, and Martin J. O’Donnell. "Regioselective hydroboration-oxidation and -amination of fluoro-substituted styrenes." Journal of Fluorine Chemistry 127, no. 9 (September 2006): 1252–55. http://dx.doi.org/10.1016/j.jfluchem.2006.06.013.
Повний текст джерелаXi, Tuo, and Zhan Lu. "Cobalt-Catalyzed Ligand-Controlled Regioselective Hydroboration/Cyclization of 1,6-Enynes." ACS Catalysis 7, no. 2 (January 10, 2017): 1181–85. http://dx.doi.org/10.1021/acscatal.6b02816.
Повний текст джерелаYao, Zi-Jian, Shibin Hong, Wei Zhang, Mengyan Liu, and Wei Deng. "Copper-catalyzed regioselective hydroboration of terminal alkynes in aqueous medium." Tetrahedron Letters 57, no. 8 (February 2016): 910–13. http://dx.doi.org/10.1016/j.tetlet.2016.01.049.
Повний текст джерелаWestcott, Stephen A., Henk P. Blom, Todd B. Marder, and R. Thomas Baker. "New homogeneous rhodium catalysts for the regioselective hydroboration of alkenes." Journal of the American Chemical Society 114, no. 23 (November 1992): 8863–69. http://dx.doi.org/10.1021/ja00049a019.
Повний текст джерелаLiu, Heng, Maxim Khononov, and Moris S. Eisen. "Catalytic 1,2-Regioselective Dearomatization of N-Heteroaromatics via a Hydroboration." ACS Catalysis 8, no. 4 (March 19, 2018): 3673–77. http://dx.doi.org/10.1021/acscatal.8b00074.
Повний текст джерелаNawasreh, Mansour. "Chemo- and regioselective hydroboration of Δ14,15 in certain cephalostatin analogue". Chinese Chemical Letters 19, № 12 (грудень 2008): 1391–94. http://dx.doi.org/10.1016/j.cclet.2008.09.055.
Повний текст джерелаYoshida, Hiroto, Ikuo Kageyuki, and Ken Takaki. "ChemInform Abstract: Silver-Catalyzed Highly Regioselective Formal Hydroboration of Alkynes." ChemInform 45, no. 51 (December 4, 2014): no. http://dx.doi.org/10.1002/chin.201451049.
Повний текст джерелаYoshida, Hiroto, Yuki Takemoto, and Ken Takaki. "A masked diboron in Cu-catalysed borylation reaction: highly regioselective formal hydroboration of alkynes for synthesis of branched alkenylborons." Chem. Commun. 50, no. 61 (2014): 8299–302. http://dx.doi.org/10.1039/c4cc01757a.
Повний текст джерелаXi, Yumeng, and John F. Hartwig. "Diverse Asymmetric Hydrofunctionalization of Aliphatic Internal Alkenes through Catalytic Regioselective Hydroboration." Journal of the American Chemical Society 138, no. 21 (May 20, 2016): 6703–6. http://dx.doi.org/10.1021/jacs.6b02478.
Повний текст джерелаOshima, Kazuyuki, Toshimichi Ohmura, and Michinori Suginome. "Regioselective Synthesis of 1,2-Dihydropyridines by Rhodium-Catalyzed Hydroboration of Pyridines." Journal of the American Chemical Society 134, no. 8 (February 17, 2012): 3699–702. http://dx.doi.org/10.1021/ja3002953.
Повний текст джерелаJin, Ji-Kang, Wan-Xin Zheng, Hui-Min Xia, Feng-Lian Zhang та Yi-Feng Wang. "Regioselective Radical Hydroboration of gem-Difluoroalkenes: Synthesis of α-Borylated Organofluorines". Organic Letters 21, № 20 (9 жовтня 2019): 8414–18. http://dx.doi.org/10.1021/acs.orglett.9b03173.
Повний текст джерелаPark, Jin Kyoon, Brian A. Ondrusek, and D. Tyler McQuade. "Regioselective Catalytic Hydroboration of Propargylic Species Using Cu(I)-NHC Complexes." Organic Letters 14, no. 18 (September 4, 2012): 4790–93. http://dx.doi.org/10.1021/ol302086v.
Повний текст джерелаZhang, Lei, Dongjie Peng, Xuebing Leng, and Zheng Huang. "Iron-Catalyzed, Atom-Economical, Chemo- and Regioselective Alkene Hydroboration with Pinacolborane." Angewandte Chemie 125, no. 13 (February 18, 2013): 3764–68. http://dx.doi.org/10.1002/ange.201210347.
Повний текст джерелаNARASIMHAN, S., K. G. PRASAD, and S. MADHAVAN. "ChemInform Abstract: Remarkable Regioselective Hydroboration of Terminal Alkenes by Calcium Borohydride." ChemInform 26, no. 25 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199525066.
Повний текст джерелаZhang, Lei, Dongjie Peng, Xuebing Leng, and Zheng Huang. "Iron-Catalyzed, Atom-Economical, Chemo- and Regioselective Alkene Hydroboration with Pinacolborane." Angewandte Chemie International Edition 52, no. 13 (February 18, 2013): 3676–80. http://dx.doi.org/10.1002/anie.201210347.
Повний текст джерелаChelvam, Venkatesh, Ramesh Reddy, and Premansh Dudhe. "Synthesis of the Deacetoxytubuvaline Fragment of Pretubulysin and its Lipophilic Analogues for Enhanced Permeability in Cancer Cell Lines." Synlett 30, no. 01 (December 6, 2018): 77–81. http://dx.doi.org/10.1055/s-0037-1611359.
Повний текст джерелаWrackmeyer, Bernd, Elena V. Klimkina, Wolfgang Milius, Christian Butterhof, and Kathrin Inzenhofer. "1,2-Hydroboration and 1,1-Carboboration of Alkynyl(ferrocenyl)vinylsilanes. Novel Siloles." Zeitschrift für Naturforschung B 69, no. 11-12 (December 1, 2014): 1269–89. http://dx.doi.org/10.5560/znb.2014-4099.
Повний текст джерелаLeong, Bi-Xiang, Jiawen Lee, Yan Li, Ming-Chung Yang, Chi-Kit Siu, Ming-Der Su, and Cheuk-Wai So. "A Versatile NHC-Parent Silyliumylidene Cation for Catalytic Chemo- and Regioselective Hydroboration." Journal of the American Chemical Society 141, no. 44 (October 10, 2019): 17629–36. http://dx.doi.org/10.1021/jacs.9b06714.
Повний текст джерелаWESTCOTT, S. A., H. P. BLOM, T. B. MARDER, and R. T. BAKER. "ChemInform Abstract: New Homogeneous Rhodium Catalysts for the Regioselective Hydroboration of Alkenes." ChemInform 24, no. 8 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199308142.
Повний текст джерелаZhu, Congjun, Jie Dong, Xueting Liu, Liuzhou Gao, Yue Zhao, Jin Xie, Shuhua Li та Chengjian Zhu. "Photoredox‐Controlled β‐Regioselective Radical Hydroboration of Activated Alkenes with NHC‐Boranes". Angewandte Chemie 132, № 31 (20 травня 2020): 12917–21. http://dx.doi.org/10.1002/ange.202005749.
Повний текст джерелаZhu, Congjun, Jie Dong, Xueting Liu, Liuzhou Gao, Yue Zhao, Jin Xie, Shuhua Li та Chengjian Zhu. "Photoredox‐Controlled β‐Regioselective Radical Hydroboration of Activated Alkenes with NHC‐Boranes". Angewandte Chemie International Edition 59, № 31 (20 травня 2020): 12817–21. http://dx.doi.org/10.1002/anie.202005749.
Повний текст джерелаWang, Xinxin, Yu Zhang, Dan Yuan, and Yingming Yao. "Regioselective Hydroboration and Hydrosilylation of N-Heteroarenes Catalyzed by a Zinc Alkyl Complex." Organic Letters 22, no. 14 (July 6, 2020): 5695–700. http://dx.doi.org/10.1021/acs.orglett.0c02082.
Повний текст джерелаZhang, Lei, Dongjie Peng, Xuebing Leng, and Zheng Huang. "ChemInform Abstract: Iron-Catalyzed, Atom-Economical, Chemo- and Regioselective Alkene Hydroboration with Pinacolborane." ChemInform 44, no. 32 (July 18, 2013): no. http://dx.doi.org/10.1002/chin.201332193.
Повний текст джерелаPark, Jin Kyoon, Brian A. Ondrusek, and D. Tyler McQuade. "ChemInform Abstract: Regioselective Catalytic Hydroboration of Propargylic Species Using Cu(I)-NHC Complexes." ChemInform 44, no. 6 (February 5, 2013): no. http://dx.doi.org/10.1002/chin.201306139.
Повний текст джерелаZhang, Congcong, Mi Zhou, Shiwen Liu, Bijia Wang, Zhiping Mao, Hong Xu, Yi Zhong, Linping Zhang, Bo Xu, and Xiaofeng Sui. "Copper-loaded nanocellulose sponge as a sustainable catalyst for regioselective hydroboration of alkynes." Carbohydrate Polymers 191 (July 2018): 17–24. http://dx.doi.org/10.1016/j.carbpol.2018.03.002.
Повний текст джерелаOshima, Kazuyuki, Toshimichi Ohmura, and Michinori Suginome. "ChemInform Abstract: Regioselective Synthesis of 1,2-Dihydropyridines by Rhodium-Catalyzed Hydroboration of Pyridines." ChemInform 43, no. 31 (July 5, 2012): no. http://dx.doi.org/10.1002/chin.201231148.
Повний текст джерела