Journal articles on the topic 'Allylic alcohols'
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Ficeri, Vlastimír, Peter Kutschy, Milan Dzurilla, and Ján Imrich. "[3,3]- Versus [1,3]-Sigmatropic Rearrangement of O-Substituted Allyl N-Acylmonothiocarbamates." Collection of Czechoslovak Chemical Communications 59, no. 12 (1994): 2650–62. http://dx.doi.org/10.1135/cccc19942650.
Full textWang, Jialiang, Wen Huang, Zhengxing Zhang, Xu Xiang, Ruiting Liu, and Xigeng Zhou. "FeCl3·6H2O Catalyzed Disproportionation of Allylic Alcohols and Selective Allylic Reduction of Allylic Alcohols and Their Derivatives with Benzyl Alcohol." Journal of Organic Chemistry 74, no. 9 (May 2009): 3299–304. http://dx.doi.org/10.1021/jo900070q.
Full textCooper, Matthew A., and A. David Ward. "Hydroxyselenation of allylic alcohols." Tetrahedron Letters 36, no. 13 (March 1995): 2327–30. http://dx.doi.org/10.1016/0040-4039(95)00247-a.
Full textHarada, Kohei, Marina Nogami, Keiichi Hirano, Daisuke Kurauchi, Hisano Kato, Kazunori Miyamoto, Tatsuo Saito, and Masanobu Uchiyama. "Allylic borylation of tertiary allylic alcohols: a divergent and straightforward access to allylic boronates." Organic Chemistry Frontiers 3, no. 5 (2016): 565–69. http://dx.doi.org/10.1039/c6qo00009f.
Full textChern, Ching-Yuh, Ching-Chun Tseng, Rong-Hong Hsiao, Fung Fuh Wong, and Yueh-Hsiung Kuo. "Cyclopentadienyl Ruthenium(II) Complex-Mediated Oxidation of Benzylic and Allylic Alcohols to Corresponding Aldehydes." Heteroatom Chemistry 2019 (August 18, 2019): 1–8. http://dx.doi.org/10.1155/2019/5053702.
Full textAkkarasamiyo, Sunisa, Somsak Ruchirawat, Poonsaksi Ploypradith, and Joseph S. M. Samec. "Transition-Metal-Catalyzed Suzuki–Miyaura-Type Cross-Coupling Reactions of π-Activated Alcohols." Synthesis 52, no. 05 (January 7, 2020): 645–59. http://dx.doi.org/10.1055/s-0039-1690740.
Full textHamada, Yoko, Rio Matsunaga, Tomoko Kawasaki-Takasuka, and Takashi Yamazaki. "Base-Mediated Claisen Rearrangement of CF3-Containing Bisallyl Ethers." Molecules 26, no. 14 (July 19, 2021): 4365. http://dx.doi.org/10.3390/molecules26144365.
Full textJun, Chul-Ho, and Chang-Hee Lee. "Chelation-Assisted C–H and C–C Bond Activation of Allylic Alcohols by a Rh(I) Catalyst under Microwave Irradiation." Synlett 29, no. 06 (November 16, 2017): 736–41. http://dx.doi.org/10.1055/s-0036-1591697.
Full textEmayavaramban, Balakumar, Moumita Roy, and Basker Sundararaju. "Iron-Catalyzed Allylic Amination Directly from Allylic Alcohols." Chemistry - A European Journal 22, no. 12 (February 17, 2016): 3952–55. http://dx.doi.org/10.1002/chem.201505214.
Full textBerger, Anna Lucia, Karsten Donabauer, and Burkhard König. "Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones." Chemical Science 9, no. 36 (2018): 7230–35. http://dx.doi.org/10.1039/c8sc02038h.
Full textParisotto, Stefano, and Annamaria Deagostino. "π-Allylpalladium Complexes in Synthesis: An Update." Synthesis 51, no. 09 (March 20, 2019): 1892–912. http://dx.doi.org/10.1055/s-0037-1611745.
Full textJing, Jiangyan, Xiaohong Huo, Jiefeng Shen, Jingke Fu, Qinghua Meng, and Wanbin Zhang. "Direct use of allylic alcohols and allylic amines in palladium-catalyzed allylic amination." Chemical Communications 53, no. 37 (2017): 5151–54. http://dx.doi.org/10.1039/c7cc01069a.
Full textMasuyama, Yoshiro, Jun P. Takahara, and Yasuhiko Kurusu. "Allylic alcohols as synthons of allylic carbanions. Palladium-catalyzed carbonyl allylation by allylic alcohols with tin dichloride." Journal of the American Chemical Society 110, no. 13 (June 1988): 4473–74. http://dx.doi.org/10.1021/ja00221a091.
Full textKang, Ye-Won, and Hye-Young Jang. "NHC-catalyzed one-pot oxidation and oxidative esterification of allylic alcohols using TEMPO: the effect of alcohol additives." RSC Adv. 4, no. 84 (2014): 44486–90. http://dx.doi.org/10.1039/c4ra08133a.
Full textMcLaughlin, Mark G., and Matthew J. Cook. "Highly diastereoselective hydrosilylations of allylic alcohols." Chem. Commun. 50, no. 26 (2014): 3501–4. http://dx.doi.org/10.1039/c4cc00138a.
Full textLuna, Hector, Kapa Prasad, and Oljan Repič. "Microbial Oxidation of Allylic Alcohols." Biocatalysis 8, no. 2 (January 1993): 155–62. http://dx.doi.org/10.3109/10242429308998202.
Full textMohamadi, Fariborz, and W. Clark Still. "Dichlorocarbene cyclopropanation of allylic alcohols." Tetrahedron Letters 27, no. 8 (January 1986): 893–96. http://dx.doi.org/10.1016/s0040-4039(00)84130-1.
Full textCahard, Dominique, Sylvain Gaillard, and Jean-Luc Renaud. "Asymmetric isomerization of allylic alcohols." Tetrahedron Letters 56, no. 45 (November 2015): 6159–69. http://dx.doi.org/10.1016/j.tetlet.2015.09.098.
Full textLevine, S. G., and N. E. Heard. "Chemical Resolution of Allylic Alcohols." Synthetic Communications 21, no. 4 (February 1991): 549–55. http://dx.doi.org/10.1080/00397919108016782.
Full textLightburn, Thomas E., Omar A. De Paolis, Ka H. Cheng, and Kian L. Tan. "Regioselective Hydroformylation of Allylic Alcohols." Organic Letters 13, no. 10 (May 20, 2011): 2686–89. http://dx.doi.org/10.1021/ol200782d.
Full textShinde, Anand H., and Shyam Sathyamoorthi. "Tethered Silanoxymercuration of Allylic Alcohols." Organic Letters 22, no. 21 (October 23, 2020): 8665–69. http://dx.doi.org/10.1021/acs.orglett.0c03257.
Full textNicolaou, K. C., Nicholas L. Simmons, Yongcheng Ying, Philipp M. Heretsch, and Jason S. Chen. "Enantioselective Dichlorination of Allylic Alcohols." Journal of the American Chemical Society 133, no. 21 (June 2011): 8134–37. http://dx.doi.org/10.1021/ja202555m.
Full textCarreira, E., and M. Roggen. "Stereospecific Substitution of Allylic Alcohols." Synfacts 2010, no. 11 (October 21, 2010): 1259. http://dx.doi.org/10.1055/s-0030-1258797.
Full textXu, Jing-Kun, Yonghong Gu, and Shi-Kai Tian. "Enantiospecific Allylic Alkylation of Substituted Hydrazines with Allylic Alcohols." Chinese Journal of Organic Chemistry 35, no. 3 (2015): 618. http://dx.doi.org/10.6023/cjoc201412049.
Full textChan, Philip, Xiaoxiang Zhang, and Weidong Rao. "Iodine-Catalyzed Allylic Alkylation of Thiols with Allylic Alcohols." Synlett 2008, no. 14 (August 2008): 2204–8. http://dx.doi.org/10.1055/s-2008-1078254.
Full textYing, Xiangxian, Yifang Wang, Bin Xiong, Tingting Wu, Liping Xie, Meilan Yu, and Zhao Wang. "Characterization of an Allylic/Benzyl Alcohol Dehydrogenase from Yokenella sp. Strain WZY002, an Organism Potentially Useful for the Synthesis of α,β-Unsaturated Alcohols from Allylic Aldehydes and Ketones." Applied and Environmental Microbiology 80, no. 8 (February 7, 2014): 2399–409. http://dx.doi.org/10.1128/aem.03980-13.
Full textQi, Juan, Guo-Tao Fan, Jie Chen, Ming-Hui Sun, Yu-Ting Dong, and Ling Zhou. "Catalytic enantioselective bromoamination of allylic alcohols." Chem. Commun. 50, no. 89 (2014): 13841–44. http://dx.doi.org/10.1039/c4cc05772d.
Full textGuo, Guozhe, Yong Yuan, Shuocheng Wan, Xuehui Cao, Yali Sun, and Congde Huo. "K2S2O8 promoted dehydrative cross-coupling between α,α-disubstituted allylic alcohols and thiophenols/thiols." Organic Chemistry Frontiers 8, no. 12 (2021): 2990–96. http://dx.doi.org/10.1039/d1qo00148e.
Full textDiscordia, Robert P., Christopher K. Murphy, and Donald C. Dittmer. "Telluride-mediated stereospecific conversion of racemic E-allylic alcohols to homochiral Z-allylic alcohols; transposition of primary and secondary allylic alcohols via glycidol derivatives." Tetrahedron Letters 31, no. 39 (1990): 5603–6. http://dx.doi.org/10.1016/s0040-4039(00)97907-3.
Full textCai, Mingzhong, Chunyun Peng, Hong Zhao, and Wenyan Hao. "A Stereoselective Synthesis of (E)-Allylic Alcohols Via the Hydromagnesiation of Alkynylsilanes." Journal of Chemical Research 2003, no. 5 (May 2003): 296–98. http://dx.doi.org/10.3184/030823403103173877.
Full textXu, Ruigang, Kai Li, Jiaqi Wang, Jiamin Lu, Lina Pan, Xiaofei Zeng, and Guofu Zhong. "Direct enantioselective allylic substitution of 4-hydroxycoumarin derivatives with branched allylic alcohols via iridium catalysis." Chemical Communications 56, no. 60 (2020): 8404–7. http://dx.doi.org/10.1039/d0cc02832k.
Full textPrieto, Consuelo, José A. González Delgado, Jesús F. Arteaga, Martín Jaraíz, José L. López-Pérez, and Alejandro F. Barrero. "Homocoupling versus reduction of radicals: an experimental and theoretical study of Ti(iii)-mediated deoxygenation of activated alcohols." Organic & Biomolecular Chemistry 13, no. 11 (2015): 3462–69. http://dx.doi.org/10.1039/c4ob02290d.
Full textAbad, Alberto, Avelino Corma, and Hermenegildo García. "Supported gold nanoparticles for aerobic, solventless oxidation of allylic alcohols." Pure and Applied Chemistry 79, no. 11 (January 1, 2007): 1847–54. http://dx.doi.org/10.1351/pac200779111847.
Full textDorta, Rosa L., María S. Rodríguez, JoséA Salazar, and Ernesto Suárez. "1,3-Transposition of primary allylic alcohols: Synthesis of optically active secondary and tertiary allylic alcohols." Tetrahedron Letters 38, no. 26 (June 1997): 4675–78. http://dx.doi.org/10.1016/s0040-4039(97)00964-7.
Full textGuo, Yunlong, and Zengming Shen. "Palladium-catalyzed allylic C–H oxidation under simple operation and mild conditions." Organic & Biomolecular Chemistry 17, no. 12 (2019): 3103–7. http://dx.doi.org/10.1039/c9ob00209j.
Full textXie, Peizhong, Zuolian Sun, Shuangshuang Li, Xinying Cai, Ju Qiu, Weishan Fu, Cuiqing Gao, Shisheng Wu, Xiaobo Yang, and Teck-Peng Loh. "Reciprocal-Activation Strategy for Allylic Sulfination with Unactivated Allylic Alcohols." Organic Letters 22, no. 12 (June 4, 2020): 4893–97. http://dx.doi.org/10.1021/acs.orglett.0c01747.
Full textLafrance, Marc, Markus Roggen, and Erick M. Carreira. "Direct, Enantioselective Iridium-Catalyzed Allylic Amination of Racemic Allylic Alcohols." Angewandte Chemie International Edition 51, no. 14 (February 17, 2012): 3470–73. http://dx.doi.org/10.1002/anie.201108287.
Full textCarreira, E., C. Defieber, M. Ariger, and P. Moriel. "Iridium-Catalyzed Synthesis of Primary Allylic Amines from Allylic Alcohols." Synfacts 2007, no. 7 (July 2007): 0731. http://dx.doi.org/10.1055/s-2007-968662.
Full textMa, Xinghua, Natasha Anderson, Lorenzo V. White, Song Bae, Warwick Raverty, Anthony C. Willis, and Martin G. Banwell. "The Conversion of Levoglucosenone into Isolevoglucosenone." Australian Journal of Chemistry 68, no. 4 (2015): 593. http://dx.doi.org/10.1071/ch14574.
Full textLiang, Xiao, Kun Wei, and Yu-Rong Yang. "Iridium-catalyzed enantioselective allylation of silyl enol ethers derived from ketones and α,β-unsaturated ketones." Chemical Communications 51, no. 98 (2015): 17471–74. http://dx.doi.org/10.1039/c5cc07221b.
Full textLi, Hongfang, Tao Li, Yu Jen Hsueh, Xue Wu, Feng Xu, and Yong Jian Zhang. "Tandem arylation and regioselective allylic etherification of 2,3-allenol via Pd/B cooperative catalysis." Organic & Biomolecular Chemistry 17, no. 35 (2019): 8075–78. http://dx.doi.org/10.1039/c9ob01792e.
Full textAntonioletti, R., F. Bonadies, L. Locati, and A. Scettri. "Zeolite-catalyzed epoxidation of allylic alcohols." Tetrahedron Letters 33, no. 22 (May 1992): 3205–6. http://dx.doi.org/10.1016/s0040-4039(00)79852-2.
Full textDonohoe, Timothy J., Peter R. Moore, Michael J. Waring, and Nicholas J. Newcombe. "The directed dihydroxylation of allylic alcohols." Tetrahedron Letters 38, no. 28 (July 1997): 5027–30. http://dx.doi.org/10.1016/s0040-4039(97)01061-7.
Full textWang, Zhi-Min, and K. Barry Sharpless. "Asymmetric dihydroxylation of tertiary allylic alcohols." Tetrahedron Letters 34, no. 51 (December 1993): 8225–28. http://dx.doi.org/10.1016/s0040-4039(00)61396-5.
Full textKang, Suk-Ku, Sung-Gyu Kim, Dong-Gyu Cho, and Jae-Ho Jeon. "Synthesis of Optically Active Allylic Alcohols." Synthetic Communications 23, no. 5 (March 1, 1993): 681–84. http://dx.doi.org/10.1080/00397919308009827.
Full textDebien, Laurent, Béatrice Quiclet-Sire, and Samir Z. Zard. "Allylic Alcohols: Ideal Radical Allylating Agents?" Accounts of Chemical Research 48, no. 5 (April 23, 2015): 1237–53. http://dx.doi.org/10.1021/acs.accounts.5b00019.
Full textLiu, Ji, Romain J. Miotto, Julien Segard, Ashley M. Erb, and Aaron Aponick. "Catalytic Dehydrative Lactonization of Allylic Alcohols." Organic Letters 20, no. 10 (May 8, 2018): 3034–38. http://dx.doi.org/10.1021/acs.orglett.8b01063.
Full textGosmini, C., T. Dubuffet, R. Sauvêtre, and J. F. Normant. "Asymmetric epoxidation of fujorinated allylic alcohols." Tetrahedron: Asymmetry 2, no. 3 (January 1991): 223–30. http://dx.doi.org/10.1016/s0957-4166(00)82361-7.
Full textZawisza, Anna Maria, Benjamin Ganchegui, Iván González, Sandrine Bouquillon, Anna Roglans, Françoise Hénin, and Jacques Muzart. "Heck-type reactions of allylic alcohols." Journal of Molecular Catalysis A: Chemical 283, no. 1-2 (March 2008): 140–45. http://dx.doi.org/10.1016/j.molcata.2007.12.021.
Full textOppong-Quaicoe, Anita A., and Brenton DeBoef. "FeCl2-Mediated Rearrangement of Allylic Alcohols." ACS Omega 4, no. 3 (March 29, 2019): 6077–83. http://dx.doi.org/10.1021/acsomega.9b00163.
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