Asymmetric Enamine CatalysisClick to copy article linkArticle link copied!
Note: In lieu of an abstract, this is the article's first page.
*
E-mail: [email protected].
Cited By
This article is cited by 2674 publications.
- Valdemar J. Enemærke, Anne Kristensen, Louise G. Rost, Esben Skovsgaard, Karl Anker Jørgensen. An Enantioselective Nucleophilic Aromatic tele-Substitution. Journal of the American Chemical Society 2025, 147
(41)
, 37854-37863. https://doi.org/10.1021/jacs.5c14328
- Subarna Jyoti Kalita, Jing Qi, Lu Xiao, Debarshi Saha, Yi-Yong Huang, Norio Shibata. Recent Advances on Catalytic Asymmetric Synthesis of Molecules Bearing a Fluorine-Containing Stereogenic Carbon Center (2015–2024). Chemical Reviews 2025, 125
(17)
, 8477-8654. https://doi.org/10.1021/acs.chemrev.5c00177
- Rong Zeng, Yu Liu, Ting Qi, Hai-Jun Leng, Xiang Zhang, Ya-Peng Wang, Wan-Cong Liu, Jun-Long Li. Enolate Activation of α-Haloaldehydes: Highly Enantioselective Aza-[4 + 2] Cyclization for the Rapid Assembly of Multifunctionalized Isothioureas. ACS Catalysis 2025, 15
(17)
https://doi.org/10.1021/acscatal.5c02739
- Dian-Feng Chen, Jin Song, Liu-Zhu Gong. Future Trends in Asymmetric Organo-Metal Combined Catalysis. ACS Central Science 2025, 11
(8)
, 1275-1288. https://doi.org/10.1021/acscentsci.5c00393
- Yuxin Ouyang, D. Quang Phan, Nikita Chekshin, Yi-Hao Li, Jennifer X. Qiao, Martin D. Eastgate, Jin-Quan Yu. Enantioselective β-C(sp3)–H Nucleophilic Tosylation of Native Amides: A Synthetic Platform for Chiral Methyl Stereocenters. Journal of the American Chemical Society 2025, 147
(23)
, 19559-19567. https://doi.org/10.1021/jacs.4c17267
- Kazuhiro Morisaki, Yuto Furuki, Rento Kousaka, Serika Nagai, Yoshihiro Oonishi, Yoshihiro Sato. Reflexive Chirality Transfer (RCT): Asymmetric 1,3-Dipolar Cycloaddition of α-Amino Acid Schiff Base with Nonchiral Copper Catalyst. Journal of the American Chemical Society 2025, 147
(15)
, 12740-12748. https://doi.org/10.1021/jacs.5c00965
- Yong Zhou, Qinman Zhang, Shuaipeng Jia, Hebo Ye, Lei You. Neighboring Chalcogen Bonding for Controlling Dynamic Imine Chemistry in Aqueous Media. Organic Letters 2025, 27
(10)
, 2438-2443. https://doi.org/10.1021/acs.orglett.5c00359
- Ádám Dudás, Ádám Gyömöre, Bence Balázs Mészáros, Stefánia Gondár, Renáta Adamik, Dániel Fegyverneki, Dávid Papp, Konrad Bernhard Otte, Sergio Ayala, Jr., János Daru, József Répási, Tibor Soós. Selective Reduction of Esters to Access Aldehydes Using Fiddler Crab-Type Boranes. Journal of the American Chemical Society 2025, 147
(1)
, 1112-1122. https://doi.org/10.1021/jacs.4c14596
- Yan Ren, Ningyuan Li, Song Liu, Dan Gao, Xiaoyu Li, Yong Luo, Yule Meng, Fuli Ye, Yidong Liu. Enantioselective Cascade Catalysis for the Construction of Tetrahydroquinolines. Organic Letters 2024, 26
(44)
, 9448-9454. https://doi.org/10.1021/acs.orglett.4c03311
- Lili Chen, Gang Liao, Bin Liu. Ligand-Enabled Nickel(II)-Catalyzed β-C(sp3)–H Thiolation of Ketones. Organic Letters 2024, 26
(42)
, 9103-9107. https://doi.org/10.1021/acs.orglett.4c03404
- Akash Sugunan, Mini Bharati Ahirwar, Cherumuttathu H. Suresh, Milind M. Deshmukh, Goreti Rajendar. Cooperative Noncovalent Interactions Controlling Amine-Catalyzed Aldol Reaction Pathways Catalyzed by the Bifunctional Amino Quaternary Phosphonium Ion. The Journal of Organic Chemistry 2024, 89
(20)
, 14851-14863. https://doi.org/10.1021/acs.joc.4c01635
- Bart Brouwer, Franco Della-Felice, Jan Hendrik Illies, Emilia Iglesias-Moncayo, Gerard Roelfes, Ivana Drienovská. Noncanonical Amino Acids: Bringing New-to-Nature Functionalities to Biocatalysis. Chemical Reviews 2024, 124
(19)
, 10877-10923. https://doi.org/10.1021/acs.chemrev.4c00136
- Yu-Ping He, Zhuo-Chen Li, Zi-Qi Wang, Wen-Ya Zheng, Hua Wu. Enamine Acylation Enabled Desymmetrization of Malonic Esters. Journal of the American Chemical Society 2024, 146
(38)
, 26387-26396. https://doi.org/10.1021/jacs.4c09276
- Kaini Xu, Yu-Shan Zhang, Bing Zhong, Long Zhang, Jin-Dong Yang, Sanzhong Luo. Organocatalytic Hydrogen Evolution Reaction by Diazaphospholenes. Journal of the American Chemical Society 2024, 146
(38)
, 25956-25962. https://doi.org/10.1021/jacs.4c10302
- Lei Yu, Jordan Diaz, Asja A. Kroeger, Michelle L. Coote, Philip Wai Hong Chan. Chiral Brønsted Acid-Catalyzed Regio-, Diastereo-, and Enantioselective Formal [2 + 2 + 2] Cycloaddition of 3-Vinyl-1H-indoles with Nitrosobenzenes. ACS Catalysis 2024, 14
(17)
, 13269-13282. https://doi.org/10.1021/acscatal.3c05041
- María-Cruz Bonache, Elisa G. -Doyagüez, Raúl Benito-Arenas, M. Angeles Bonache, María-Luisa Jimeno, Ana San-Félix. Skeletal Transformations Observed in the Reaction of a Tricyclic Thymine Nucleoside with Dicarbonyl Compounds. ACS Omega 2024, 9
(34)
, 36259-36272. https://doi.org/10.1021/acsomega.4c02553
- Hongjiang Li, Chunxiang Pan, Xinhan Li, Zhenxiu He, Xueyan Sun, Jianbin Xu, Kaimin Wang, Baomin Fan. Photocatalytic Hantzsch Ester-Mediated Pinacol-Type Coupling of Aldehydes and Ketones. The Journal of Organic Chemistry 2024, 89
(16)
, 11537-11541. https://doi.org/10.1021/acs.joc.4c01233
- Jia Zhang, Kai Hin Lui, Rachele Zunino, Yuan Jia, Romain Morodo, Niklas Warlin, James L. Hedrick, Giovanni Talarico, Robert M. Waymouth. Highly Selective O-Phenylene Bisurea Catalysts for ROP: Stabilization of Oxyanion Transition State by a Semiflexible Hydrogen Bond Pocket. Journal of the American Chemical Society 2024, 146
(32)
, 22295-22305. https://doi.org/10.1021/jacs.4c04740
- Soumyadip Hore, Jiwoo Jeong, Dongwook Kim, Sukbok Chang. Visible-Light-Promoted Enantioselective α-Amidation of Aldehydes by Harnessing Organo-Iron Dual Catalysis. Journal of the American Chemical Society 2024, 146
(32)
, 22172-22179. https://doi.org/10.1021/jacs.4c07884
- Juan Tang, Shun Li, Yihua Fu, Zhishan Su, Jiaqi Xu, Weichao Xue, Xueli Zheng, Ruixiang Li, Hua Chen, Haiyan Fu. Radical meta-C–H Halogenation of Azines via N-Benzyl Activation Strategy. Organic Letters 2024, 26
(28)
, 5899-5904. https://doi.org/10.1021/acs.orglett.4c01643
- Greta Vastakaite, Alena Budinská, Claude L. Bögli, Linus B. Boll, Helma Wennemers. Kinetic Resolution of β-Branched Aldehydes through Peptide-Catalyzed Conjugate Addition Reactions. Journal of the American Chemical Society 2024, 146
(28)
, 19101-19107. https://doi.org/10.1021/jacs.4c03617
- Sudip Guria, Alexander N. Volkov, Raffi Khudaverdyan, Ruben Van Lommel, Rittwika Pan, Constantin G. Daniliuc, Frank De Proft, Ulrich Hennecke. Enantioselective, Bro̷nsted Acid-Catalyzed Anti-selective Hydroamination of Alkenes. Journal of the American Chemical Society 2024, 146
(25)
, 17180-17188. https://doi.org/10.1021/jacs.4c03306
- Rohtash Kumar, Vidyasagar Maurya, Avinash Avinash, Chandrakumar Appayee. Nonsilyl Bicyclic Secondary Amine Catalysts for the Asymmetric Transfer Hydrogenation of α,β-Unsaturated Aldehydes. The Journal of Organic Chemistry 2024, 89
(12)
, 8586-8600. https://doi.org/10.1021/acs.joc.4c00523
- Michael Weiser, Ádám Márk Pálvölgyi, Matthias Weil, Katharina Bica-Schröder. Continuous Enantioselective α-Alkylation of Ketones via Direct Photoexcitation. The Journal of Organic Chemistry 2024, 89
(12)
, 8906-8914. https://doi.org/10.1021/acs.joc.4c00759
- Mao Cai, Long Zhang, Wenzhao Zhang, Qifeng Lin, Sanzhong Luo. Enantioselective Transformations by “1 + x” Synergistic Catalysis with Chiral Primary Amines. Accounts of Chemical Research 2024, 57
(10)
, 1523-1537. https://doi.org/10.1021/acs.accounts.4c00128
- Reilly Osadchey Brown, Darren Demapan, Qiang Cui. Complete Computational Reaction Mechanism for Foldamer-Catalyzed Aldol Condensation. ACS Catalysis 2024, 14
(10)
, 7624-7638. https://doi.org/10.1021/acscatal.4c00937
- Tülay Yıldız, Belma Hasdemir, Hasniye Yaşa, Hatice Başpınar Küçük. New Strategy for the Synthesis of Some Valuable Chiral 1,3-Diols with High Enantiomeric Purity: New Organocatalyst, Asymmetric Aldol Reaction, and Reduction. ACS Omega 2024, 9
(11)
, 12657-12664. https://doi.org/10.1021/acsomega.3c07948
- Wei Wen, Qi-Xiang Guo. Chiral Aldehyde Catalysis-Enabled Asymmetric α-Functionalization of Activated Primary Amines. Accounts of Chemical Research 2024, 57
(5)
, 776-794. https://doi.org/10.1021/acs.accounts.3c00804
- Enfu Wang, Jiangbin Luo, Luoman Zhang, Jian Zhang, Yaojia Jiang. Copper-Catalyzed Oxidative [3 + 2] Cycloaddition of Enamines and Pyridotriazoles toward Indolizines. Organic Letters 2024, 26
(6)
, 1249-1254. https://doi.org/10.1021/acs.orglett.4c00063
- Kangmei Wen, Chen Chen, Weiya Kong, Qiwen Gao, Jie Shi, Xiaodong Tang. Cooperative Triple Catalysis Enables Deaminative α-Indolmethylation of Carbonyl Compounds with Gramines. The Journal of Organic Chemistry 2024, 89
(2)
, 1064-1072. https://doi.org/10.1021/acs.joc.3c02170
- Pooja Sah, Aakash Kumar Gond, Gaurav Saini, Manmohan Kapur. A Sequential Transition Metal and Organocatalytic Approach to the Enantioselective Synthesis of C2-Spiroindoline Systems. Organic Letters 2023, 25
(51)
, 9170-9175. https://doi.org/10.1021/acs.orglett.3c03716
- Wennan Dong, Zhifei Zhao, Cheng-Zhi Gu, Jing-Gong Liu, Shuang Yang, Xinqiang Fang. Copper-Catalyzed Umpolung Reactivity of Propargylic Carbonates in the Presence of Diboronates: One Stone Four Birds. Journal of the American Chemical Society 2023, 145
(50)
, 27539-27554. https://doi.org/10.1021/jacs.3c09155
- Akash Sugunan, V. M. Aparna, Goreti Rajendar. Phosphonium Ion-Tethered Secondary Amines for Chemospecific 5-Enolexo Aldol Condensations of 6-Ketoaldehydes. The Journal of Organic Chemistry 2023, 88
(24)
, 17472-17478. https://doi.org/10.1021/acs.joc.3c02285
- Surendra Saini, Pratibha Saini, Krishan Kumar, Mukul Sethi, Priyanka Meena, Aditya Gurjar, Anshu Dandia, Tanya Dhuria, Vijay Parewa. Unlocking the Molecular Behavior of Natural Amine-Targeted Carbon Quantum Dots for the Synthesis of Diverse Pharmacophore Scaffolds via an Unusual Nanoaminocatalytic Route. ACS Applied Materials & Interfaces 2023, 15
(42)
, 49083-49094. https://doi.org/10.1021/acsami.3c08812
- Seonil Kim, Seongryeol Jeung, Sarah Yunmi Lee. Stereodivergent Conjugate Addition between Iminium and α-Azaaryl α-Fluoroenolate Intermediates by Synergistic Amine and Lewis Acid Catalysis. ACS Catalysis 2023, 13
(20)
, 13838-13845. https://doi.org/10.1021/acscatal.3c03121
- Maximilian Bechtel, Marian Ebeling, Laura Huber, Oliver Trapp. (Photoredox) Organocatalysis in the Emergence of Life: Discovery, Applications, and Molecular Evolution. Accounts of Chemical Research 2023, 56
(20)
, 2801-2813. https://doi.org/10.1021/acs.accounts.3c00396
- Benjamin D. A. Shennan, Sergio Sánchez-Alonso, Gabriele Rossini, Darren J. Dixon. 1,2-Redox Transpositions of Tertiary Amides. Journal of the American Chemical Society 2023, 145
(40)
, 21745-21751. https://doi.org/10.1021/jacs.3c08466
- Zhen Li, Xiao-Ming Zhang, Fu-Min Zhang, Yong-Qiang Tu. Catalytic Enantioselective Alkylation of Aldehydes with 3-Bromooxindoles. Organic Letters 2023, 25
(39)
, 7252-7257. https://doi.org/10.1021/acs.orglett.3c02882
- Yannick Brägger, Ori Green, Benjamin N. Bhawal, Bill Morandi. Late-Stage Molecular Editing Enabled by Ketone Chain-Walking Isomerization. Journal of the American Chemical Society 2023, 145
(36)
, 19496-19502. https://doi.org/10.1021/jacs.3c05680
- Yuvraj Garg, James Osborne, Serhii Vasylevskyi, Nivedha Velmurugan, Fujie Tanaka. 1,3-Diamine-Derived Catalysts: Design, Synthesis, and the Use in Enantioselective Mannich Reactions of Ketones. The Journal of Organic Chemistry 2023, 88
(15)
, 11096-11101. https://doi.org/10.1021/acs.joc.3c01051
- David Weinzierl, Magdalena Piringer, Paul Zebrowski, Lotte Stockhammer, Mario Waser. Photochemical Wolff Rearrangement Initiated Generation and Subsequent α-Chlorination of C1 Ammonium Enolates. Organic Letters 2023, 25
(17)
, 3126-3130. https://doi.org/10.1021/acs.orglett.3c00986
- Andrew J. Neel, Zhuqing Liu, Tamas Benkovics, Lu Wang, Stephan M. Rummelt, Heather C. Johnson, Kevin M. Belyk, Feng Xu, Cheol K. Chung, David J. Lamberto, Ryan D. Cohen, Stephanus Axnanda, Zachary E. X. Dance. Development of a Kilogram-Scale Synthesis of a Key Ulevostinag Subunit Part II: An Electrophilic Approach to Fluorinated Nucleosides. Organic Process Research & Development 2023, 27
(3)
, 458-469. https://doi.org/10.1021/acs.oprd.2c00395
- Yongbing Liu, Huanlin Diao, Guorong Hong, Jonathan Edward, Tao Zhang, Guoqiang Yang, Bin-Miao Yang, Yu Zhao. Iridium-Catalyzed Enantioconvergent Borrowing Hydrogen Annulation of Racemic 1,4-Diols with Amines. Journal of the American Chemical Society 2023, 145
(9)
, 5007-5016. https://doi.org/10.1021/jacs.2c09958
- Qian Liu, Kunpeng Teng. Facile Approach for the Oxidative Enolate Activation of Aliphatic Aldehydes. The Journal of Organic Chemistry 2023, 88
(4)
, 2404-2414. https://doi.org/10.1021/acs.joc.2c02821
- N. Samali Weliwatte, Hui Chen, Tianhua Tang, Shelley D. Minteer. Three-Stage Conversion of Chemically Inert n-Heptane to α-Hydrazino Aldehyde Based on Bioelectrocatalytic C–H Bond Oxyfunctionalization. ACS Catalysis 2023, 13
(1)
, 563-572. https://doi.org/10.1021/acscatal.2c04003
- Ming-Zhu Lu, Jeffrey Goh, Manikantha Maraswami, Zhenhua Jia, Jie-Sheng Tian, Teck-Peng Loh. Recent Advances in Alkenyl sp2 C–H and C–F Bond Functionalizations: Scope, Mechanism, and Applications. Chemical Reviews 2022, 122
(24)
, 17479-17646. https://doi.org/10.1021/acs.chemrev.2c00032
- Yuta Yamagiwa, Masafumi Harada, Hiroshi Yao. Strong Chiroptical Activity in Cobalt Oxide/Hydroxide Nanoparticles Passivated by Chiral Nonthiol Amino Acid Proline. The Journal of Physical Chemistry C 2022, 126
(50)
, 21308-21318. https://doi.org/10.1021/acs.jpcc.2c06837
- Zhiqiang Zhou, Dongyang Xu, Wei Jiang, Junhan Chen, Yanxia Zhen, Jiyou Huo, Jiahang Yan, Jinming Gao, Weiqing Xie. Convergent Synthesis of Enantioenriched ortho-Fused Tricyclic Diketones via Catalytic Asymmetric Intramolecular Vinylogous Aldol Condensation. Organic Letters 2022, 24
(49)
, 9017-9022. https://doi.org/10.1021/acs.orglett.2c03645
- Holly McErlain, Euan B. McLean, Timaeus E. F. Morgan, Valeria K. Burianova, Adriana A. S. Tavares, Andrew Sutherland. Organocatalytic Asymmetric Synthesis of SynVesT-1, a Synaptic Density Positron Emission Tomography Imaging Agent. The Journal of Organic Chemistry 2022, 87
(21)
, 14443-14451. https://doi.org/10.1021/acs.joc.2c01895
- Robert E. Wiley, Michael F. McLaughlin, Jeffrey S. Johnson. Dearomatization of Cyclic Diphenylhydrazines: Harnessing the o-Semidine Rearrangement for the Synthesis of Spirocyclic Tetrahydroquinolines. Organic Letters 2022, 24
(43)
, 8014-8018. https://doi.org/10.1021/acs.orglett.2c03220
- Andrew J. Neel, Ben W. H. Turnbull, William P. Carson, Tamas Benkovics, Cheol K. Chung, Heather C. Johnson, Zhuqing Liu, Feng Peng, Stephan M. Rummelt, Zhiguo Jake Song, Lushi Tan, Lu Wang, Feng Xu. A Unified Strategy to Fluorinated Nucleoside Analogues Via an Electrophilic Manifold. Organic Letters 2022, 24
(41)
, 7701-7706. https://doi.org/10.1021/acs.orglett.2c03367
- Wanying Zhang, Jingjing Hu, Siwei Bi, Baoping Ling, Xiang-Ai Yuan, Yuan-Ye Jiang. Insights into α-Alkynylation and α-Allenylation of Aldehydes under the Synergisitic Catalysis of Gold/Amine: A DFT Study. The Journal of Organic Chemistry 2022, 87
(19)
, 13102-13110. https://doi.org/10.1021/acs.joc.2c01596
- Jiajun Wang, Jigneshkumar Dahyabhai Prajapati, Fan Gao, Yi-Lun Ying, Ulrich Kleinekathöfer, Mathias Winterhalter, Yi-Tao Long. Identification of Single Amino Acid Chiral and Positional Isomers Using an Electrostatically Asymmetric Nanopore. Journal of the American Chemical Society 2022, 144
(33)
, 15072-15078. https://doi.org/10.1021/jacs.2c03923
- Wenzhong Li, Ran Shi, Xuesi Zhang, Sen Chen, Yu Wang, Mengqi Wang, Bin Yang, Jiazhu Li, Xin-Ming Xu. Different Lewis Acid Promotor-Steered Highly Regioselective Phosphorylation of Tertiary Enamides. The Journal of Organic Chemistry 2022, 87
(15)
, 9769-9781. https://doi.org/10.1021/acs.joc.2c00829
- Yue Dong, Xiangmin Li, Peng Ji, Feng Gao, Xiang Meng, Wei Wang. Synthesis of C-1 Deuterated 3-Formylindoles by Organophotoredox Catalyzed Direct Formylation of Indoles with Deuterated Glyoxylic Acid. Organic Letters 2022, 24
(28)
, 5034-5039. https://doi.org/10.1021/acs.orglett.2c01768
- Katsuhiko Moriyama, Yukari Oka. Enantioselective Cascade Michael/Hemiaminal Formation of α,β-Unsaturated Iminoindoles with Aldehydes Using a Chiral Aminomethylpyrrolidine Catalyst Bearing a SO2C6F5 Group as a Strongly Electron Withdrawing Arylsulfonyl Group. ACS Catalysis 2022, 12
(12)
, 7436-7442. https://doi.org/10.1021/acscatal.2c01182
- Wei Gong, Zhijie Chen, Jinqiao Dong, Yan Liu, Yong Cui. Chiral Metal–Organic Frameworks. Chemical Reviews 2022, 122
(9)
, 9078-9144. https://doi.org/10.1021/acs.chemrev.1c00740
- Hengfu Xu, Richard N. Schaugaard, Jiayi Li, H. Bernhard Schlegel, Hien M. Nguyen. Stereoselective 1,2-cis Furanosylations Catalyzed by Phenanthroline. Journal of the American Chemical Society 2022, 144
(16)
, 7441-7456. https://doi.org/10.1021/jacs.2c02063
- David Guzmán Ríos, Miguel A. Romero, José A. González-Delgado, Jesús F. Arteaga, Uwe Pischel. Metal-Mediated Organocatalysis in Water: Serendipitous Discovery of Aldol Reaction Catalyzed by the [Ru(bpy)2(nornicotine)2]2+ Complex. The Journal of Organic Chemistry 2022, 87
(8)
, 5412-5418. https://doi.org/10.1021/acs.joc.2c00472
- Liubo Li, Anton El Khoury, Brennan O’Neil Clement, Carolyn Wu, Patrick G. Harran. Asymmetric Organocatalysis Enables Rapid Assembly of Portimine Precursor Chains. Organic Letters 2022, 24
(14)
, 2607-2612. https://doi.org/10.1021/acs.orglett.2c00556
- Philip L. Hahn, Jared M. Lowe, Yubo Xu, Kevin L. Burns, Michael K. Hilinski. Amine Organocatalysis of Remote, Chemoselective C(sp3)–H Hydroxylation. ACS Catalysis 2022, 12
(8)
, 4302-4309. https://doi.org/10.1021/acscatal.2c00392
- Renwei Zhang, Meng Sun, Qiaolin Yan, Xingbang Lin, Xin Li, Xin Fang, Herman H. Y. Sung, Ian D. Williams, Jianwei Sun. Asymmetric Synthesis of Pyrrolidines via Oxetane Desymmetrization. Organic Letters 2022, 24
(12)
, 2359-2364. https://doi.org/10.1021/acs.orglett.2c00564
- Shovan Mondal, Frédéric Dumur, Didier Gigmes, Mukund P. Sibi, Michèle P. Bertrand, Malek Nechab. Enantioselective Radical Reactions Using Chiral Catalysts. Chemical Reviews 2022, 122
(6)
, 5842-5976. https://doi.org/10.1021/acs.chemrev.1c00582
- Yue-Xiao Wu, Ming-Hui Huang, Kang Peng, Zhen Shi, Er-jun Hao, Zhi-Bing Dong. One-Pot Synthesis of Benzoazole-Substituted Thioenamines via a Cross Dehydrogenation Coupling (CDC) Reaction. The Journal of Organic Chemistry 2022, 87
(5)
, 2446-2455. https://doi.org/10.1021/acs.joc.1c02353
- Yao Li, Long Zhang, Sanzhong Luo. Bond Energies of Enamines. ACS Omega 2022, 7
(7)
, 6354-6374. https://doi.org/10.1021/acsomega.1c06945
- Mary Katherine Andrews, Xinyu Liu, Samuel H. Gellman. Tailoring Reaction Selectivity by Modulating a Catalytic Diad on a Foldamer Scaffold. Journal of the American Chemical Society 2022, 144
(5)
, 2225-2232. https://doi.org/10.1021/jacs.1c11542
- Aleksandra Topolska, Sebastian Frankowski, Łukasz Albrecht. Differentiating Catalysis in the Dearomative [4 + 2]-Cycloaddition Involving Enals and Heteroaromatic Aldehydes. Organic Letters 2022, 24
(3)
, 955-959. https://doi.org/10.1021/acs.orglett.1c04328
- Virgil Hélaine, Cédric Gastaldi, Marielle Lemaire, Pere Clapés, Christine Guérard-Hélaine. Recent Advances in the Substrate Selectivity of Aldolases. ACS Catalysis 2022, 12
(1)
, 733-761. https://doi.org/10.1021/acscatal.1c04273
- Sandeep Kumar Sharma, Alilugatta Sheshagiri Rao Paniraj, Yashwant Bhikaji Tambe. Developments in the Catalytic Asymmetric Synthesis of Agrochemicals and Their Synthetic Importance. Journal of Agricultural and Food Chemistry 2021, 69
(49)
, 14761-14780. https://doi.org/10.1021/acs.jafc.1c05553
- Rémi Blieck, Sébastien Lemouzy, Arie van der Lee, Marc Taillefer, Florian Monnier. Synergistic Copper/Enamine Catalysis for the Regio-, Stereo-, and Enantioselective Intermolecular α-Addition of Aldehydes to Allenamides. Organic Letters 2021, 23
(23)
, 9199-9203. https://doi.org/10.1021/acs.orglett.1c03477
- Noor U Din Reshi, Vitthal B. Saptal, Matthias Beller, Jitendra K. Bera. Recent Progress in Transition-Metal-Catalyzed Asymmetric Reductive Amination. ACS Catalysis 2021, 11
(22)
, 13809-13837. https://doi.org/10.1021/acscatal.1c04208
- E. H. Nisala Fernando, Jose Cortes Vazquez, Jacqkis Davis, Weiwei Luo, Vladimir N. Nesterov, Hong Wang. Can Primary Arylamines Form Enamine? Evidence, α-Enaminone, and [3+3] Cycloaddition Reaction. The Journal of Organic Chemistry 2021, 86
(21)
, 14617-14626. https://doi.org/10.1021/acs.joc.1c01462
- Andreas Kunzendorf, Guangcai Xu, Jesse J. H. van der Velde, Henriëtte J. Rozeboom, Andy-Mark W. H. Thunnissen, Gerrit J. Poelarends. Unlocking Asymmetric Michael Additions in an Archetypical Class I Aldolase by Directed Evolution. ACS Catalysis 2021, 11
(21)
, 13236-13243. https://doi.org/10.1021/acscatal.1c03911
- Zhen-Hua Wang, Pei-Sen Gao, Xiu Wang, Jun-Qing Gao, Xue-Tao Xu, Zeng He, Cong Ma, Tian-Sheng Mei. TEMPO-Enabled Electrochemical Enantioselective Oxidative Coupling of Secondary Acyclic Amines with Ketones. Journal of the American Chemical Society 2021, 143
(38)
, 15599-15605. https://doi.org/10.1021/jacs.1c08671
- Nicolò Tampellini, Paolo Righi, Giorgio Bencivenni. Computational Investigation on the Origin of Atroposelectivity for the Cinchona Alkaloid Primary Amine-Catalyzed Vinylogous Desymmetrization of N-(2-t-Butylphenyl)maleimides. The Journal of Organic Chemistry 2021, 86
(17)
, 11782-11793. https://doi.org/10.1021/acs.joc.1c01235
- Timothy B. Wright, P. Andrew Evans. Catalytic Enantioselective Alkylation of Prochiral Enolates. Chemical Reviews 2021, 121
(15)
, 9196-9242. https://doi.org/10.1021/acs.chemrev.0c00564
- Masanori Yoshida. Organocatalytic Asymmetric α-Allylation and Propargylation of α-Branched Aldehydes with Alkyl Halides. The Journal of Organic Chemistry 2021, 86
(15)
, 10921-10927. https://doi.org/10.1021/acs.joc.1c01394
- Tian-Yuan Zhao, Ke Li, Liang-Liang Yang, Shou-Fei Zhu, Qi-Lin Zhou. Nickel-Catalyzed Desymmetrizing Cyclization of 1,6-Dienes to Construct Quaternary Stereocenters. Organic Letters 2021, 23
(10)
, 3814-3817. https://doi.org/10.1021/acs.orglett.1c00796
- Fangfang Guo, Jiean Chen, Yong Huang. A Bifunctional N-Heterocyclic Carbene as a Noncovalent Organocatalyst for Enantioselective Aza-Michael Addition Reactions. ACS Catalysis 2021, 11
(10)
, 6316-6324. https://doi.org/10.1021/acscatal.1c01908
- Gabriel J. Roeder, H. Ray Kelly, Guoju Yang, Thomas J. Bauer, Gary L. Haller, Victor S. Batista, Eszter Baráth. Selective Heterogeneous Transfer Hydrogenation from Tertiary Amines to Alkynes. ACS Catalysis 2021, 11
(9)
, 5405-5415. https://doi.org/10.1021/acscatal.0c05186
- Wanjun Chen, Yaping Cheng, Tao Zhang, Yu Mu, Wenqi Jia, Guodu Liu. Ni/AntPhos-Catalyzed Stereoselective Asymmetric Intramolecular Reductive Coupling of N-1,6-Alkynones. The Journal of Organic Chemistry 2021, 86
(7)
, 5166-5182. https://doi.org/10.1021/acs.joc.1c00079
- Vidyasagar Maurya, Mahesh S. Kutwal, Chandrakumar Appayee. Direct Catalytic Asymmetric Synthesis of Disubstituted 4-Oxocyclohexanecarbaldehydes from Acetone and Cinnamaldehyde Derivatives. Organic Letters 2021, 23
(5)
, 1566-1571. https://doi.org/10.1021/acs.orglett.0c04277
- Jasmine Sinha, Shafer Soars, Christopher N. Bowman. Enamine Organocatalysts for the Thiol-Michael Addition Reaction and Cross-Linking Polymerizations. Macromolecules 2021, 54
(4)
, 1693-1701. https://doi.org/10.1021/acs.macromol.0c02128
- Donggeon Nam, Viktoria Steck, Robert J. Potenzino, Rudi Fasan. A Diverse Library of Chiral Cyclopropane Scaffolds via Chemoenzymatic Assembly and Diversification of Cyclopropyl Ketones. Journal of the American Chemical Society 2021, 143
(5)
, 2221-2231. https://doi.org/10.1021/jacs.0c09504
- Yejin Chang, Min Cao, Jessica Z. Chan, Cunyuan Zhao, Yuankai Wang, Rose Yang, Masayuki Wasa. Enantioselective Synthesis of N-Alkylamines through β-Amino C–H Functionalization Promoted by Cooperative Actions of B(C6F5)3 and a Chiral Lewis Acid Co-Catalyst. Journal of the American Chemical Society 2021, 143
(5)
, 2441-2455. https://doi.org/10.1021/jacs.0c13200
- Kai-Ge Wen, Chao Liu, Dong-Hui Wei, Yan-Fei Niu, Yi-Yuan Peng, Xing-Ping Zeng. Catalytic Enantioselective Desymmetrization of Cyclobutane-1,3-diones by Carbonyl-Amine Condensation. Organic Letters 2021, 23
(3)
, 1118-1122. https://doi.org/10.1021/acs.orglett.1c00067
- Mao Cai, Kaini Xu, Yuze Li, Zongxiu Nie, Long Zhang, Sanzhong Luo. Chiral Primary Amine/Ketone Cooperative Catalysis for Asymmetric α-Hydroxylation with Hydrogen Peroxide. Journal of the American Chemical Society 2021, 143
(2)
, 1078-1087. https://doi.org/10.1021/jacs.0c11787
- Byungjun Kim, Yongjae Kim, Sarah Yunmi Lee. Stereodivergent Carbon–Carbon Bond Formation between Iminium and Enolate Intermediates by Synergistic Organocatalysis. Journal of the American Chemical Society 2021, 143
(1)
, 73-79. https://doi.org/10.1021/jacs.0c11077
- Barry M. Trost, Chuanle Zhu. Zn-ProPhenol Catalyzed Enantioselective Mannich Reaction of 2H-Azirines with Alkynyl Ketones. Organic Letters 2020, 22
(24)
, 9683-9687. https://doi.org/10.1021/acs.orglett.0c03737
- Tapas Kumar Achar, Sudip Maiti, Sadhan Jana, Debabrata Maiti. Transition Metal Catalyzed Enantioselective C(sp2)–H Bond Functionalization. ACS Catalysis 2020, 10
(23)
, 13748-13793. https://doi.org/10.1021/acscatal.0c03743
- Gonglin Li, Mohuizi Liu, Sijia Zou, Xiaoming Feng, Lili Lin. A Bispidine-Based Chiral Amine Catalyst for Asymmetric Mannich Reaction of Ketones with Isatin Ketimines. Organic Letters 2020, 22
(21)
, 8708-8713. https://doi.org/10.1021/acs.orglett.0c03305
- Zebediah C. Girvin, Samuel H. Gellman. Foldamer Catalysis. Journal of the American Chemical Society 2020, 142
(41)
, 17211-17223. https://doi.org/10.1021/jacs.0c07347
- Jia-Li Liu, Jia-Lin Tu, Feng Liu. Visible-Light-Promoted Intramolecular α-Allylation of Aldehydes in the Absence of Sacrificial Hydrogen Acceptors. Organic Letters 2020, 22
(18)
, 7369-7372. https://doi.org/10.1021/acs.orglett.0c02742
- Raveendra Jillella, Selvam Raju, Huan-Chang Hsiao, Day-Shin Hsu, Shih-Ching Chuang. Pd-Catalyzed Redox-Neutral C–N Coupling Reaction of Iminoquinones with Electron-Deficient Alkenes without External Oxidants: Access of Tertiary (E)-Enamines and Application to the Synthesis of Indoles and Quinolin-4-ones. Organic Letters 2020, 22
(16)
, 6252-6256. https://doi.org/10.1021/acs.orglett.0c01929
- Barry M. Trost, Jacob S. Tracy. Catalytically Generated Vanadium Enolates Formed via Interruption of the Meyer–Schuster Rearrangement as Useful Reactive Intermediates. Accounts of Chemical Research 2020, 53
(8)
, 1568-1579. https://doi.org/10.1021/acs.accounts.0c00285
- Gabriela G. Gerosa, Maribel O. Marcarino, Rolando A. Spanevello, Alejandra G. Suárez, Ariel M. Sarotti. Re-Engineering Organocatalysts for Asymmetric Friedel–Crafts Alkylation of Indoles through Computational Studies. The Journal of Organic Chemistry 2020, 85
(15)
, 9969-9978. https://doi.org/10.1021/acs.joc.0c01256
- Cristian Rosso, Giacomo Filippini, Maurizio Prato. Carbon Dots as Nano-Organocatalysts for Synthetic Applications. ACS Catalysis 2020, 10
(15)
, 8090-8105. https://doi.org/10.1021/acscatal.0c01989
- Xingxing Ma, Xiaoxia Yu, Hua Huang, Yao Zhou, Qiuling Song. Synthesis of Thiazoles and Isothiazoles via Three-Component Reaction of Enaminoesters, Sulfur, and Bromodifluoroacetamides/Esters. Organic Letters 2020, 22
(14)
, 5284-5288. https://doi.org/10.1021/acs.orglett.0c01275
- Alberto Martinez-Cuezva, Adrian Saura-Sanmartin, Mateo Alajarin, Jose Berna. Mechanically Interlocked Catalysts for Asymmetric Synthesis. ACS Catalysis 2020, 10
(14)
, 7719-7733. https://doi.org/10.1021/acscatal.0c02032
- Lili Chen, Yuhuan Yang, Luhua Liu, Qian Gao, Senmiao Xu. Iridium-Catalyzed Enantioselective α-C(sp3)–H Borylation of Azacycles. Journal of the American Chemical Society 2020, 142
(28)
, 12062-12068. https://doi.org/10.1021/jacs.0c06756
Article Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.
Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.
The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated.