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Visible-Light Induced Radical Addition–Elimination Reaction for Constructing Allylic Sulfones from Sulfonyl Chlorides and Allyl Bromides J. Org. Chem. (IF 3.6) Pub Date : 2024-03-27 Rui-Xue Li, Yuan Chen, Lan-Qian Huang, Zhi Guan, Yan-Hong He
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Dissymmetrical Chiral Peropyrenes: Synthesis via Iridium-Catalyzed C–H Activation/Alkyne Benzannulation and Study of Their Properties J. Org. Chem. (IF 3.6) Pub Date : 2024-03-27 Stephen P. George, Jonas Spengler, Ryan J. Malone, James Krzoska, Frank Würthner, Wesley A. Chalifoux
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Resin-Immobilized Palladium Acetate and Alcohol Dehydrogenase for Chemoenzymatic Enantioselective Synthesis of Chiral Diarylmethanols J. Org. Chem. (IF 3.6) Pub Date : 2024-03-27 Yanyan Li, Guanhua Liu, Liya Zhou, Li Ma, Ying He, Jing Gao, Yanjun Jiang, Limei Ren, Yunting Liu
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InCl3/TfOH-Mediated Convenient Synthesis of 3-Alkylideneoxindoles from 2-Oxindoles with 1,3-Diones, Ketones, or Aldehydes J. Org. Chem. (IF 3.6) Pub Date : 2024-03-27 Xia Chen, Xiao-Yu Zhou, Hai-Long Liu, Chao Ding, Jin-Hui Li
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General Synthesis of Conformationally Constrained Noncanonical Amino Acids with C(sp3)-Rich Benzene Bioisosteres J. Org. Chem. (IF 3.6) Pub Date : 2024-03-26 Xiaoshen Ma, Adam M. Beard, Samantha A. Burgess, Miroslawa Darlak, Justin A. Newman, Lisa M. Nogle, Mark J. Pietrafitta, David A. Smith, Xiao Wang, Lei Yue
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A Tandem Ring Closure and Nitrobenzene Reduction with Sulfide Provides an Improved Route to an Important Intermediate for the Anti-Tuberculosis Drug Candidate Sutezolid Org. Process Res. Dev. (IF 3.4) Pub Date : 2024-03-27 Hanuman P. Kalmode, Ongolu Ravikumar, Dinesh J. Paymode, John Bachert, Justina M. Burns, Rodger W. Stringham, Sarah L. Aleshire, Ryan C. Nelson
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Palladium-Catalyzed Regioselective Insertion of Carbenes into γ-C(sp3)–H Bonds of Aliphatic Amines Org. Lett. (IF 5.2) Pub Date : 2024-03-27 Peng Zhang, Cheng-xin Li, ShihaoZhi Wang, Xue-jing Zhang, Ming Yan
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Highly Contorted Rigid Nitrogen-Rich Nanographene with Four Heptagons Org. Lett. (IF 5.2) Pub Date : 2024-03-27 Abdusalom A. Suleymanov, Qilin He, Peter Müller, Timothy M. Swager
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Leveraging Nonstrained C–C Bonds for Selective Carboacylation of an Unactivated Alkyne via Transient Dearomatization Org. Lett. (IF 5.2) Pub Date : 2024-03-27 Jiamin He, Tongxiang Cao, Kai Chen, Shifa Zhu
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Oxidative Control of Photoinduced Cascade Electrocyclizations in Aromatic Azido Imines to Access Complex Fused Imidazoles or Pyrazoles Org. Lett. (IF 5.2) Pub Date : 2024-03-26 D. Sai Reddy, Ivan M. Novitskiy, Anastasia A. Beloglazkina, Andrei G. Kutateladze
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SO2F2-Mediated Thioesterification of Carboxylic Acids with Thiols Eur. J. Org. Chem. (IF 2.8) Pub Date : 2024-03-26 Guofu Zhang, Huijie Qi, Chenfei Guan, Hui Jin, Ying Zhou, Chengrong Ding
The generation of thioesters through thioesterification of carboxylic acid has significant synthetic value given the easy availability of various carboxylic acids and the extensive application of thioesters. An economical and rapid thioester synthesis approach is still needed. Herein, we achieved thioesterification of carboxylic acids with valuable glycosyl thiol, aromatic and aliphatic thiols mediated
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Palladium Catalyzed Carbonyl Amination of Fluorinated Olefins for Synthesis of α-CF3-Acrylamides Eur. J. Org. Chem. (IF 2.8) Pub Date : 2024-03-27 Yang Li, Yu Jing, Yi-Ran Shi, Hong Li, Min-Ge Yang, Yong-Li Kou, Qiang-Wei Fan
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Recent Advances in the Metal Catalyzed Asymmetric Alkene Hydrogenation of Cyclic Conjugated Carbonyl Compounds Org. Chem. Front. (IF 5.4) Pub Date : 2024-03-27 Min Tan, Bram B. C. Peters, Pher Andersson, Taigang Zhou
The transition metal catalyzed asymmetric hydrogenation of carbon-carbon double bonds is recognized as one of the most straightforward methods for the preparation of stereopure compounds. Chiral cyclic motifs have widespread applications in organic synthesis and can also be prepared via this strategy. This review summarizes the recent advances (2016-2023) in the stereoselective metal catalyzed hydrogenation
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A Mn(III)-catalyzed arylboronic acid-based cascade reaction via a nonclassical organometallic-radical mechanism Org. Chem. Front. (IF 5.4) Pub Date : 2024-03-22 Hui-Min Qian, Jian-Dong Zhang, Shun-Jun Ji, Xiao-Ping Xu
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Synthesis of multisubstituted carbazol-4-amines from tetrahydrocarbazol-4-one oximes Org. Chem. Front. (IF 5.4) Pub Date : 2024-03-22 Jiahua Wang, Dandan Gao, Aanuoluwapo O. Oyejobi, Na Ji, Xiang-Ying Tang, Long Wang
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Inubritantrimers A–D: Trimerized Sesquiterpenoid [4 + 2] Adducts Featuring a Distinctive Spiro-Polycyclic Scaffold from Inula britannica J. Org. Chem. (IF 3.6) Pub Date : 2024-03-26 Cong Guo, Ruo-Yu Qi, Jie-Yi Ren, Dan-Dan Xu, Qiang Zhang, Jin-Ming Gao, Jiang-Jiang Tang
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Correction to “Robust Chemical Synthesis of ‘Difficult Peptides’ via 2-Hydroxyphenol-pseudoproline (ψ2-hydroxyphenolpro) Modifications” J. Org. Chem. (IF 3.6) Pub Date : 2024-03-26 Xinyue Wang, Kang Jin
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Efficient Multikilogram-Scale Synthesis of PTDSS1 Inhibitor: Development of a Practical and Scalable Optical Resolution Method for Chiral 2,3-Pyrrolidinedione Org. Process Res. Dev. (IF 3.4) Pub Date : 2024-03-26 Keisuke Suzuki, Ryusei Itoh, Jo Oyama, Masaki Hayashi, Tsuyoshi Ueda
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Synthesis of Helical-Shaped Axially Chiral Bisoxime Ethers via Chiral Phosphoric-Acid-Catalyzed Sequential Enantioselective Condensations Org. Lett. (IF 5.2) Pub Date : 2024-03-26 Bing-ru Shao, Bai-hao Ren, Wen-feng Jiang, Lei Shi
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Catalytic System-Controlled Regioselective 1,2- and 1,4-Carboannulations of [60]Fullerene Org. Lett. (IF 5.2) Pub Date : 2024-03-25 Tong-Xin Liu, Yifei Ru, Wenyue Guo, Nana Ma, Panting Yang, Xiaojun Li, Pengling Zhang, Jingjing Bi, Guisheng Zhang
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Copper-Catalyzed Site-Selective Electrophilic Aromatic Alkylation of Monosubstituted Simple Arenes Org. Lett. (IF 5.2) Pub Date : 2024-03-24 Wanting Fu, Jing Tian, Yuanli Ding, Xi Wang, Meiyan Wang, Zikun Wang
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DNA-Compatible Functional Group Transformations via K2RuO4-mediated Oxidation Org. Chem. Front. (IF 5.4) Pub Date : 2024-03-26 Pengyang He, Guixian Zhao, Mengping Zhu, Yangfeng Li, Gong Zhang, Yizhou Li
Functional group transformation represents a potent strategy for enriching the chemical diversity in DNA-encoded chemical library (DEL) synthesis. Within the realm of functional group transformation reactions, oxidation stands out as a predominant and facile approach to deliver altered chemical reactivity. However, reports on DNA-compatible oxidative reactions facilitating functional group transformations
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Palladium-catalyzed [4+4] cycloaddition of 2-pyrones with 2-alkylidenetrimethylene carbonates: access to bridged eight-membered oxygen heterocycles Org. Chem. Front. (IF 5.4) Pub Date : 2024-03-26 Huawei Lin, Biming Mao, Bing Han, Jiayi Luo, Yanqing Ge, Xuerui Zhang, Chang Wang, Hongchao Guo, Chunhao Yuan
In this work, a wide range of bridged eight-membered oxygen heterocycles have been constructed through a novel palladium-catalyzed [4+4] cycloaddition of 2-pyrones with 2-alkylidenetrimethylene carbonates. The reaction demonstrated broad substrate scope and afforded the products in good yields with excellent stereoselectivity.
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Synthesis of 3,5-Disubstituted-1,2,4-thiadiazoles via NaH–DMF-Promoted Dehydrogenative Intramolecular N–S Bond Formation J. Org. Chem. (IF 3.6) Pub Date : 2024-03-26 Mary Antony P., Jeevan Chakravarthy A. S., Hiriyakkanavar Ila
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Strongly Polarized π-Extended 1,4-Dihydropyrrolo[3,2-b]pyrroles Fused with Tetrazolo[1,5-a]quinolines J. Org. Chem. (IF 3.6) Pub Date : 2024-03-26 Mohammad B. Teimouri, Irena Deperasińska, Matt Rammo, Marzena Banasiewicz, Charles W. Stark, Łukasz Dobrzycki, Michał K. Cyrański, Aleksander Rebane, Daniel T. Gryko
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Correction to “Catalyst- and Base-Free Synthesis of Morita–Baylis–Hillman and Rauhut–Currier Adducts of β-Aminonitroalkenes” J. Org. Chem. (IF 3.6) Pub Date : 2024-03-26 Snehal Pednekar, Sudheesh T. Sivanandan, Deepak Kumar, Raveendran Bharath Krishna, Irishi N. N. Namboothiri
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Rhodium(I)/Chiral Diene Complexes Catalyzed Asymmetric Desymmetrization of Alkynyl-Tethered 2,5-Cyclohexadienones Through an Arylative Cyclization Cascade J. Org. Chem. (IF 3.6) Pub Date : 2024-03-25 Yu-Yi Cheng, Ting-Shen Kuo, Ping-Yu Wu, Jen-Chieh Hsieh, Hsyueh-Liang Wu
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Development and Scale-Up of a Key Copper-Catalyzed Biaryl Ether Formation for the Multikilogram Synthesis of Emprumapimod Org. Process Res. Dev. (IF 3.4) Pub Date : 2024-03-26 Christopher Brearley, Robert David Bright, James Clarke, Douglas J. Critcher, Susana Torres, Ingrid Edwards, Harriet Fenton, Shanjun Huang, Rebecca Amy Johnson, Ricky A. Jones, Suju P. Mathew, Rhys Norster, Kathryn Alice Starbuck, Amelia Taylor-Young, William Waddington, Robert Walton, Jimmy Wang
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QbD Approach to Process Characterization and Quantitative Criticality Assessment of Process Parameters† Org. Process Res. Dev. (IF 3.4) Pub Date : 2024-03-25 Pankaj D. Rege, Andreas Schuster, Jens Lamerz, Christian Moessner, Wolfgang Göhring, Pirmin Hidber, Helmut Stahr, Oana Mihaela Andrei, Janine Burren, Alexandre Moesching, Daniel Coleman, Stefan Hildbrand
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A New Process To Prepare Thiophene-2-Carbonyl Chloride, a Key Raw Material in the Synthesis of Tioxazafen, Utilizing a Catalytic Liquid Phase Aerobic Oxidation Reaction Org. Process Res. Dev. (IF 3.4) Pub Date : 2024-03-25 Daniel P. Walker, Kevin J. Koeller, William H. Miller, Charles R. Graham, G. Davis Harris, Jr., Swati Nigudkar, George H. Klemm, Wensheng Li
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Asparaginyl Endopeptidase-Mediated Peptide Cyclization for Phage Display Org. Lett. (IF 5.2) Pub Date : 2024-03-26 Xiao-Cui Wan, Yan-Ni Zhang, Hua Zhang, Ying Chen, Zhi-Hui Cui, Wen-Jing Zhu, Ge-Min Fang
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Total Synthesis of Cyclotripeptidic Natural Products Anacine, Aurantiomide C, Polonimides A and C, and Verrucine F Org. Lett. (IF 5.2) Pub Date : 2024-03-26 Guanghui Han, Wei Zhang, Emmanuelle Acs, Alexis Paquin, Quentin Ronzon, Nicolas Casaretto, Bastien Nay
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Accessing Benzoazepine Derivatives via Photoinduced Radical Relay Formal [5 + 2] Reaction of Amide/Alkyne Enabled by Palladium Catalysis Org. Lett. (IF 5.2) Pub Date : 2024-03-26 Yu-jia Du, Xia-xin Sheng, Lu-ning Tang, Jia-ming Chen, Guo-ying Liu, Hao Hu, Sen Yang, Lei Zhu, Ming Chen
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Manganese Pentacarbonyl Bromide as Regeneration Catalyst Enabled Biomimetic Asymmetric Reduction Org. Lett. (IF 5.2) Pub Date : 2024-03-25 Zheng Liu, Yan-Jiang Yu, Yu-Qing Bai, Mu-Wang Chen, Yong-Gui Zhou
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A Simple Nickel Metal–Organic Framework-Catalyzed Borylation of Aryl Chlorides and Bromides Org. Lett. (IF 5.2) Pub Date : 2024-03-25 Aishwarya Prakash, Suma Basappa, Bhavya Jeebula, Doddahalli H. Nagaraju, Rajendra S. Dhayal, Shubhankar Kumar Bose
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Regio- and Diastereoselective Radical Dimerization Reactions for the Construction of Benzo[f]isoindole Dimers Org. Lett. (IF 5.2) Pub Date : 2024-03-25 Chuanchuan Wang, Jingyi Lin, Haiyang Huang, Changqing Ye, Hongli Bao
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Gold-Catalyzed Cascade Cycloisomerization of 3-Allyloxy-1,6-diynes to Cyclopropyl- and Cyclobutyl-Fused Benzofurans and Chromen-3a(1H)-ols Org. Lett. (IF 5.2) Pub Date : 2024-03-25 Zeliang Wang, Jichao Chen, Lei Yu, Chunyu Zhang, Weidong Rao, Philip Wai Hong Chan
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Photoredox-Catalyzed Acylchlorination of α-CF3 Alkenes with Acyl Chloride and Application as Masked Access to β-CF3-enones Org. Lett. (IF 5.2) Pub Date : 2024-03-25 Youkang Zhou, Qi Jiang, Yangyang Cheng, Mingyou Hu, Xin-Hua Duan, Le Liu
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Thiol-Triggered Tandem Dearomative Michael Addition/Intramolecular Henry Reaction of 2-Nitrobenzofurans: Access to Sulfur-Containing Polyheterocyclic Compounds Org. Lett. (IF 5.2) Pub Date : 2024-03-24 Jun-Rui Zhuo, Jian-Qiang Zhao, Lei Yang, Yu-Lu Wu, Yan-Ping Zhang, Yong You, Zhen-Hua Wang, Ming-Qiang Zhou, Wei-Cheng Yuan
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Highly selective separation of toluene/methylcyclohexane based on pagoda[5]arene nonporous adaptive crystals Org. Chem. Front. (IF 5.4) Pub Date : 2024-03-26 Zhongwen Liu, Ming Li, Shuai Fang, Li Shao, Bin Hua, Feihe Huang
Highly selective separation of toluene (Tol) over methylcyclohexane (MCH) has been achieved by utilizing nonporous adaptive crystals of pagoda[5]arene P5. Specifically, P5 demonstrates not only superior binding capability for Tol in solution, but also excellent selectivity for separating Tol from an equivolume Tol/MCH mixture with a high purtiy of 98.8%.
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Photoredox Catalyzed Hydroazolylation of Alkenes via Phosphoranyl Radicals Org. Chem. Front. (IF 5.4) Pub Date : 2024-03-26 Fan Zhu, Zhi Qiao, Na He, Chunxiao Nong, Qiping He, Meilan Xi, Xizhong Song, Jun Lin, Jingbo Chen, Yi Jin
Herein, a general protocol for the hydroazolylation of alkenes with N-hydroxyl azoles is reported. These reactions proceed via a phosphoranyl radical that is accessed by photoredox catalysis, followed by radical coupling of the resulting azole radical to the alkenes radical. The key point of this reaction lies in the specific binding between the hydroxy group on N-hydroxyazole and alkyl phosphine.
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DBU-Catalyzed Substitution-Controlled Synthesis of Oxa[3.3.1] Bridged Ring and Naphthylamine Derivatives Org. Chem. Front. (IF 5.4) Pub Date : 2024-03-26 Shiyu Xu, Zhihui Sun, Pengyutian Liu, Yuanlin Wei, Fan Sun, Man Zhao, Ying Wang, Ming Zhang, Guofeng Li, Hong Liang
A switchable cascade cyclization reaction of ortho-alkynyl arylketones with amines has been developed. The different reaction pathways are controlled by the substituent of the α-carbon of in-situ generated ortho-alkynyl arylaldimines. Under the catalysis of DBU, the oxa[3.3.1] bridged ring compounds and 1-naphthylamine derivatives are obtained with high yields and excellent regioselectivities. This
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Synthesis of 10B-enriched 2,1-borazaronaphthalenes from o-aminostyrenes and 10BF3 Org. Chem. Front. (IF 5.4) Pub Date : 2024-03-26 Weihua Qiu, Jide Zhu, Rencai Tao, Kai Yang, Qiuling Song
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C–H activation-enabled synthesis of a piperazine-embedded azadibenzo[a,g]corannulene analogue Org. Chem. Front. (IF 5.4) Pub Date : 2024-03-21 Lin Huang, Mengyu Qiu, Zhihao Chang, Duncan L. Browne, Jianhui Huang
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Regioselective Synthesis of the Tetrahydrocarbazole Core of Akuammiline Alkaloids via Palladium-Catalyzed Intramolecular Arylation Reaction J. Org. Chem. (IF 3.6) Pub Date : 2024-03-25 Naga M. R. Vampugani, Ajay B. Shelke, Prashant B. Singh, Asrar Ahmad, Ajoy Kapat
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Mechanism of Asymmetric Homologation of Alkenylboronic Acids with CF3-Diazomethane via Borotropic Rearrangement J. Org. Chem. (IF 3.6) Pub Date : 2024-03-25 Maria Biosca, Kálmán J. Szabó, Fahmi Himo
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Conformational Isomerization as a Process to Determine Selectivity over Reaction Pathways: Effect of Alkene Rotation in Chain Walking via Cis Alkene Intermediates J. Org. Chem. (IF 3.6) Pub Date : 2024-03-25 Kazuma Muto, Miho Hatanaka, Fumitoshi Kakiuchi, Takuya Kochi
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Synthesis, Resolution, and Absolute Configuration of a Phosphine-Based Hemicryptophane Cage with an Endo Phosphorus Lone Pair and Formation of the Corresponding Gold Complex J. Org. Chem. (IF 3.6) Pub Date : 2024-03-25 Marc Hennebelle, Yoann Cirillo, Anne-Doriane Manick, Didier Nuel, Alexandre Martinez, Bastien Chatelet
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Photocatalytic Proton-Coupled Electron Transfer Enabled Radical Cyclization for Isoquinoline-1,3-diones Synthesis J. Org. Chem. (IF 3.6) Pub Date : 2024-03-25 Wenjuan Zhang, Yaqi Song, Tian-Yu Sun, Dawei Wang, Xiao-Feng Xia
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Phosphine-Catalyzed [4 + 3] Annulation of β′-Acetoxy Allenoates with 1C,3N-Dinucleophiles: Access to Functionalized Azepine Derivatives J. Org. Chem. (IF 3.6) Pub Date : 2024-03-24 Chunjie Ni, Zhanhang Liang, Xiaojuan Xu, Fan Yu, Dong Zhang, Chen Chen
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Cesium Carbonate Promoted Direct Amidation of Unactivated Esters with Amino Alcohol Derivatives J. Org. Chem. (IF 3.6) Pub Date : 2024-03-24 Chih-Hung Kuo, Wen-Tsai Hsieh, Ya-Hsu Yang, Teng-Li Hwang, Yu-Shan Cheng, Yuya A. Lin
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Dehydrogenative N‐N Coupling and Facile Synthesis of Cobalt Complexes Supported by Tetrazene Based Ligand: Synthesis of Quinolines and Quinazolinones via Activation of Alcohols Eur. J. Org. Chem. (IF 2.8) Pub Date : 2024-03-26 Sheela Kumari, Ankur Maji, Rahul Chauhan, Virendra K. Chaudhary, Tapasya Kush, Mayank Joshi, Angshuman R. Choudhury, Kaushik Ghosh
Herein we first report the unprecedented synthesis of tetrazene‐based cobalt complexes using unusual coupling of amines via dehydrogenation. These cobalt complexes were employed for dehydrogenative coupling reactions to synthesize N‐heterocycles (quinoline, and quinazolinone). Based on control experiments and IR identification of intermediates, we proposed a plausible reaction mechanism. Synthesis
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Platform for 3-fluoro-3-hydroxyoxindoles: photocatalytic C–N cross-coupling and deaminative oxidation–fluorohydroxylation Org. Chem. Front. (IF 5.4) Pub Date : 2024-03-25 Letian Zhang, Yibin Wang, Jiabin Shen, Hao Xu, Chao Shen
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The synthesis of isoxazolines and dihydrooxazines by Pd-catalyzed oxyalkynylation alkenyl oximes with alkynyl bromides Org. Chem. Front. (IF 5.4) Pub Date : 2024-03-25 Cangzhu Hu, Shiji Xu, Qiang Wang, Jing Sun, Ying Han, Chao-Guo Yan, Lei Wang
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Recent Advances in the Direct N–C(sp2) Nitrone Synthesis from Oxime Eur. J. Org. Chem. (IF 2.8) Pub Date : 2024-03-25 Kosaku Tanaka
Nitrones are pivotal in organic chemistry, especially for the synthesis of natural and biologically active compounds via 1,3‐dipolar cycloadditions and Kinugasa reactions. Although numerous methods have been reported for the synthesis of nitrones with an sp3 carbon connected to a nitrogen atom, the development of nitrones with an sp2 carbon linkage, including N‐vinyl, N‐aryl, and N‐alkoxycarbonyl nitrones
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Exploring the Reactivity of Melanins as Photocatalysts for Reductive Dehalogenations Eur. J. Org. Chem. (IF 2.8) Pub Date : 2024-03-25 Andrea Capucciati, Valentina Foli, Pasquale Lioniello, Maria Laura Alfieri, Elena Cassera, Daniele Merli, Paola Manini, Davide Ravelli
Four melanin polymers prepared from different precursors (5,6‐dihydroxyindole, 5,6‐dihydroxyindole 2‐carboxylic acid, 1,8‐dihydroxynaphthalene and dopamine) have been adopted as photocatalysts in the reductive dehalogenation of a series of model a‐halogen carbonyl derivatives. The best performing melanin was that obtained from 5,6‐dihydroxyindole 2‐carboxylic acid, which allowed to dehalogenate efficiently
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Commercial transaminases for the asymmetric synthesis of bulky amines. Eur. J. Org. Chem. (IF 2.8) Pub Date : 2024-03-25 Marianne Bore Haarr, Kotchakorn T.sriwong, Elaine O'Reilly
Transaminase‐catalysed asymmetric amination is a valuable transformation for the synthesis of chiral amines. However, its use in synthetic chemistry has been curtailed by a narrow substrate scope and limited information on commercially available catalysts. In this work we have explored the substrate scope of selected commercially available transaminases, focusing on prochiral ketones bearing two bulky
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Polymorphism and White Light Emission of 1‐Bromo‐3,5,7‐triphenyladamantane Compared with 1,3,5,7‐Tetraphenyladamantane Eur. J. Org. Chem. (IF 2.8) Pub Date : 2024-03-25 Saravanan Gowrisankar, Andrey A Fokin, Jonathan Becker, Neeshma Mathew, Jörn Schmedt auf der Günne, Peter Richard Schreiner
Here we report our investigation of 1‐bromo‐3,5,7‐triphenyladamantane (1) and the elucidation of polymorphic crystals (1A and 1B) using single crystal X‐ray diffraction. In the monoclinic crystal system of 1A (P21/n), we observed CH−π interactions, while Br···Br interactions are absent. Conversely, the Br···Br interactions are an apparent factor in the formation of the monoclinic crystal system of
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Stereocontrolled Synthesis of Phosphoproline Analogues Containing a trans-Fused Octahydroindole Bicyclic System J. Org. Chem. (IF 3.6) Pub Date : 2024-03-22 R. Israel Hernández-Benítez, José Luis Viveros-Ceballos, Mario Ordoñez, Victoria Labastida-Galván
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Addition to “Regioselective 1,2-Alkylboration of Benzylidenecyclopropanes: Access to Csp3-Enriched Cyclopropyl Boronic Esters” Org. Lett. (IF 5.2) Pub Date : 2024-03-22 Pinku Prasad Mondal, Anagha Veluthanath Nair, Megha Sasidaran, Alvin Antony Chungath, Satya Prakash Suman, Rositha Kuniyil, Basudev Sahoo
The file of atomic coordinates was inadvertently left out of the Supporting Information because of a journal production error and not an oversight by the authors. The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acs.orglett.4c00814. Coordinates (XYZ) Most electronic Supporting Information files are available without a subscription to ACS Web Editions. Such