Статті в журналах з теми "C–N atropisomers"
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Xiao, Xiao, Biao Chen, Yi-Ping Yao, Hai-Jie Zhou, Xu Wang, Neng-Zhong Wang, and Fen-Er Chen. "Construction of Non-Biaryl Atropisomeric Amide Scaffolds Bearing a C–N Axis via Enantioselective Catalysis." Molecules 27, no. 19 (October 4, 2022): 6583. http://dx.doi.org/10.3390/molecules27196583.
Повний текст джерелаBonne, Damien, and Jean Rodriguez. "Enantioselective syntheses of atropisomers featuring a five-membered ring." Chemical Communications 53, no. 92 (2017): 12385–93. http://dx.doi.org/10.1039/c7cc06863h.
Повний текст джерелаWang, Donglei, Qianwen Jiang, and Xiaoyu Yang. "Atroposelective synthesis of configurationally stable nonbiaryl N–C atropisomers through direct asymmetric aminations of 1,3-benzenediamines." Chemical Communications 56, no. 46 (2020): 6201–4. http://dx.doi.org/10.1039/d0cc02368j.
Повний текст джерелаFaisca Phillips, Ana Maria, and Armando J. L. Pombeiro. "Atropselective Organocatalytic Synthesis of Chiral Compounds Containing Nitrogen along the Axis of Chirality." Symmetry 15, no. 6 (June 15, 2023): 1261. http://dx.doi.org/10.3390/sym15061261.
Повний текст джерелаJiayong, Zhang, and Liu Xin-Yuan. "Single-Step Synthesis of Atropisomers with Vicinal C—C and C—N Diaxes via Cobalt-Catalyzed C—H Activation." Chinese Journal of Organic Chemistry 42, no. 11 (2022): 3899. http://dx.doi.org/10.6023/cjoc202200062.
Повний текст джерелаMonteiro, Carlos J. P., Mariette M. Pereira, Nuno P. F. Gonçalves, Carla G. Carvalho, Ângela C. B. Neves, Artur R. Abreu, Luis G. Arnaut, and Artur M. S. Silva. "Separation and atropisomer isolation of ortho-halogenated tetraarylporphyrins by HPLC: Full characterization using 1D and 2D NMR." Journal of Porphyrins and Phthalocyanines 16, no. 03 (March 2012): 316–23. http://dx.doi.org/10.1142/s1088424612500368.
Повний текст джерелаJia, Zhen-Sheng, Yong-Jie Wu, Qi-Jun Yao, Xue-Tao Xu, Kun Zhang, and Bing-Feng Shi. "Pd(II)-Catalyzed Atroposelective C–H Allylation: Synthesis of Enantioenriched N-Aryl Peptoid Atropisomers." Organic Letters 24, no. 1 (December 29, 2021): 304–8. http://dx.doi.org/10.1021/acs.orglett.1c03967.
Повний текст джерелаWu, Yong-Jie, Pei-Pei Xie, Gang Zhou, Qi-Jun Yao, Xin Hong, and Bing-Feng Shi. "Atroposelective synthesis of N-aryl peptoid atropisomers via a palladium(ii)-catalyzed asymmetric C–H alkynylation strategy." Chemical Science 12, no. 27 (2021): 9391–97. http://dx.doi.org/10.1039/d1sc01130h.
Повний текст джерелаHasegawa, Futoshi, Kazushi Kawamura, Hiroshi Tsuchikawa, and Michio Murata. "Stable C–N axial chirality in 1-aryluracil scaffold and differences in in vitro metabolic clearance between atropisomers of PDE4 inhibitor." Bioorganic & Medicinal Chemistry 25, no. 16 (August 2017): 4506–11. http://dx.doi.org/10.1016/j.bmc.2017.06.042.
Повний текст джерелаBain, Alex D., Hao Chen, and Paul H. M. Harrison. "Studies of structure and dynamics in a nominally symmetric twisted amide by NMR and electronic structure calculations." Canadian Journal of Chemistry 84, no. 3 (March 1, 2006): 421–28. http://dx.doi.org/10.1139/v06-016.
Повний текст джерелаKnipe, Peter C., and Jamie S. Sweet. "Catalytic Enantioselective Synthesis of C–N Atropisomeric Heterobiaryls." Synthesis 54, no. 09 (February 23, 2022): 2119–32. http://dx.doi.org/10.1055/s-0040-1719896.
Повний текст джерелаMcCormick, Theresa M., Qinde Liu, and Suning Wang. "Luminescent Atropisomeric N,N-Chelating Ligands from Copper-Catalyzed One-Pot C−N and C−C Coupling Reactions." Organic Letters 9, no. 21 (October 2007): 4087–90. http://dx.doi.org/10.1021/ol701485a.
Повний текст джерелаChen, Yao-Zhong, Teng Liu, Jie Zhu, Hui Zhang, and Lei Wu. "Transition-metal-free radical cleavage of a hydrazonyl N–S bond: tosyl radical-initiated cascade C(sp3)–OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation." Organic Chemistry Frontiers 5, no. 24 (2018): 3567–73. http://dx.doi.org/10.1039/c8qo00873f.
Повний текст джерелаSaid, Awad I., and Talaat I. El-Emary. "Diastereoselective synthesis of atropisomeric pyrazolyl pyrrolo[3,4-d]isoxazolidines via pyrazolyl nitrone cycloaddition to facially divergent maleimides: intensive NMR and DFT studies." RSC Advances 10, no. 2 (2020): 845–50. http://dx.doi.org/10.1039/c9ra10039c.
Повний текст джерелаKöster, Roland, Günther Seidel, Susanna Kerschl, and Bernd Wrackmeyer. "Atropisomerism in Boron-Nitrogen Heterocycles/Atropisomerism in Boron-Nitrogen Heterocycles." Zeitschrift für Naturforschung B 42, no. 2 (February 1, 1987): 191–94. http://dx.doi.org/10.1515/znb-1987-0212.
Повний текст джерелаTakahashi, Isao, Yuya Suzuki, and Osamu Kitagawa. "Asymmetric Synthesis of Atropisomeric Compounds with an N‒C Chiral Axis." Organic Preparations and Procedures International 46, no. 1 (January 2014): 1–23. http://dx.doi.org/10.1080/00304948.2014.866467.
Повний текст джерелаLi, Zhaojie, and Shouyun Yu. "Asymmetric synthesis of atropisomeric compounds with C–N chiral axis." SCIENTIA SINICA Chimica 50, no. 5 (April 22, 2020): 509–25. http://dx.doi.org/10.1360/ssc-2019-0168.
Повний текст джерелаFan, Xiaozhong, Xue Zhang, Chunyu Li, and Zhenhua Gu. "Enantioselective Atropisomeric Anilides Synthesis via Cu-Catalyzed Intramolecular Adjacent C–N Coupling." ACS Catalysis 9, no. 3 (January 31, 2019): 2286–91. http://dx.doi.org/10.1021/acscatal.8b04789.
Повний текст джерелаOtotake, Nobutaka, Yudai Morimoto, Ayano Mokuya, Haruhiko Fukaya, Yasuo Shida, and Osamu Kitagawa. "Catalytic Enantioselective Synthesis of Atropisomeric Indoles with an NC Chiral Axis." Chemistry - A European Journal 16, no. 23 (May 12, 2010): 6752–55. http://dx.doi.org/10.1002/chem.201000243.
Повний текст джерелаChiba, Arisa, Ryoko Tanaka, Mayuno Hotta, Kayo Nakamura, Kosho Makino, Hidetsugu Tabata, Tetsuta Oshitari, Hideaki Natsugari, and Hideyo Takahashi. "Stereochemistry of N-Acyl-5H-dibenzo[b,d]azepin-7(6H)-ones." Molecules 28, no. 12 (June 13, 2023): 4734. http://dx.doi.org/10.3390/molecules28124734.
Повний текст джерелаShi, Bing-Feng, and Françoise Colobert. "Perfect control of C–N atropisomeric axis for creating high-added-value compounds." Chem Catalysis 1, no. 3 (August 2021): 485–87. http://dx.doi.org/10.1016/j.checat.2021.07.008.
Повний текст джерелаTakahashi, Isao, Yuya Suzuki, and Osamu Kitagawa. "ChemInform Abstract: Asymmetric Synthesis of Atropisomeric Compounds with an N-C Chiral Axis." ChemInform 45, no. 14 (March 21, 2014): no. http://dx.doi.org/10.1002/chin.201414248.
Повний текст джерелаMöhrle, H., and M. Jeandrée. "Darstellung und Atropisomerie von 1-[2-(2,2-Dimethylpiperidino)phenyl]ethanol." Scientia Pharmaceutica 69, no. 1 (March 30, 2001): 1–10. http://dx.doi.org/10.3797/scipharm.aut-01-01.
Повний текст джерелаTakahashi, Isao, Fumika Morita, Shunsuke Kusagaya, Haruhiko Fukaya, and Osamu Kitagawa. "Catalytic enantioselective synthesis of atropisomeric 2-aryl-4-quinolinone derivatives with an N–C chiral axis." Tetrahedron: Asymmetry 23, no. 24 (December 2012): 1657–62. http://dx.doi.org/10.1016/j.tetasy.2012.11.004.
Повний текст джерелаTakeshita, Hitoshi, Akira Mori, Yukari Ikeda, and Nobuo Kato. "C–N Bond Atropisomerism of 1-(2,4-Dimethyl-3-pentyl)cyclohepta[b]pyrrol-2(1H)-one." Chemistry Letters 19, no. 12 (December 1990): 2199–200. http://dx.doi.org/10.1246/cl.1990.2199.
Повний текст джерелаMatsui, Ryosuke, Erina Niijima, Tomomi Imai, Hiroyuki Kobayashi, Akiko Hori, Azusa Sato, Yuko Nakamura, and Osamu Kitagawa. "Intermolecular Halogen Bond Detected in Racemic and Optically Pure N-C Axially Chiral 3-(2-Halophenyl)quinazoline-4-thione Derivatives." Molecules 27, no. 7 (April 6, 2022): 2369. http://dx.doi.org/10.3390/molecules27072369.
Повний текст джерелаZhang, Kan, Yuqi Liu, Zhikun Shang, Corey Evans, and Shengfu Yang. "Effects of End-Caps on the Atropisomerization, Polymerization, and the Thermal Properties of ortho-Imide Functional Benzoxazines." Polymers 11, no. 3 (March 1, 2019): 399. http://dx.doi.org/10.3390/polym11030399.
Повний текст джерелаMino, Takashi, Youichi Tanaka, Youtaro Hattori, Motoko Tanaka, Masami Sakamoto, and Tsutomu Fujita. "Synthesis of N-Aryl Indolines from 2-Fluorobenzaldehyde Dimethylhydrazone Derivatives: Approach to Preparation of C(aryl)-N(Amine) Bond Atropisomeric Amines." Letters in Organic Chemistry 1, no. 1 (January 1, 2004): 67–69. http://dx.doi.org/10.2174/1570178043488699.
Повний текст джерелаMino, Takashi, Haruka Yamada, Shingo Komatsu, Mizuki Kasai, Masami Sakamoto, and Tsutomu Fujita. "Atropisomerism at C-N Bonds of Acyclic Amines: Synthesis and Application to Palladium-Catalyzed Asymmetric Allylic Alkylations." European Journal of Organic Chemistry 2011, no. 24 (July 12, 2011): 4540–42. http://dx.doi.org/10.1002/ejoc.201100769.
Повний текст джерелаKlvaňa, Robert, Radek Pohl, Jan Pawlas, Jan Čejka, Hana Dvořáková, Richard Hrabal, Stanislav Böhm, Bohumil Kratochvíl, and Josef Kuthan. "Sterically Crowded Heterocycles. XII. Atropisomerism of (1-Aryl-3,5-diphenyl-1H-pyrrol-2-yl)(phenyl)methanones." Collection of Czechoslovak Chemical Communications 65, no. 5 (2000): 651–66. http://dx.doi.org/10.1135/cccc20000651.
Повний текст джерелаKwon, Yongseok, and Ahreum Kim. "Catalytic Atroposelective Dynamic Kinetic Resolution of Substituted Indoles." Synlett 33, no. 03 (November 11, 2021): 201–6. http://dx.doi.org/10.1055/a-1694-4695.
Повний текст джерелаTakahashi, Isao, Fumika Morita, Shunsuke Kusagaya, Haruhiko Fukaya, and Osamu Kitagawa. "ChemInform Abstract: Catalytic Enantioselective Synthesis of Atropisomeric 2-Aryl-4-quinolinone Derivatives with an N-C Chiral Axis." ChemInform 44, no. 23 (May 16, 2013): no. http://dx.doi.org/10.1002/chin.201323139.
Повний текст джерелаTAKESHITA, H., A. MORI, Y. IKEDA, and N. KATO. "ChemInform Abstract: C-N Bond Atropisomerism of 1-(2,4-Dimethyl-3-pentyl)cyclohepta(b) pyrrol-2(1H)-one." ChemInform 23, no. 5 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199205176.
Повний текст джерелаJwad, Rasha S., Alan H. C. Pang, Luke Hunter, and Roger W. Read. "In Pursuit of Fluorinated Sigma Receptor Ligand Candidates Related to [18F]-FPS." Australian Journal of Chemistry 72, no. 3 (2019): 213. http://dx.doi.org/10.1071/ch18510.
Повний текст джерелаWezeman, Tim, Yuling Hu, John McMurtrie, Stefan Bräse, and Kye-Simeon Masters. "Synthesis of Non-Symmetrical and Atropisomeric Dibenzo[1,3]diazepines: Pd/CPhos-Catalysed Direct Arylation of Bis-Aryl Aminals." Australian Journal of Chemistry 68, no. 12 (2015): 1859. http://dx.doi.org/10.1071/ch15465.
Повний текст джерелаTakahashi, Masashi, and Osamu Kitagawa. "Catalytic Enantioselective Synthesis of Novel Atropisomeric Compounds having an N-C Chiral Axis and Their Application to Asymmetric Reaction." Journal of Synthetic Organic Chemistry, Japan 69, no. 9 (2011): 985–93. http://dx.doi.org/10.5059/yukigoseikyokaishi.69.985.
Повний текст джерелаMino, Takashi, Youichi Tanaka, Toshihiro Yabusaki, Daisuke Okumura, Masami Sakamoto, and Tsutomu Fujita. "A C(aryl)N(amine) bond atropisomeric aminophosphine: preparation and use as a ligand in a catalytic asymmetric allylic alkylation." Tetrahedron: Asymmetry 14, no. 17 (September 2003): 2503–6. http://dx.doi.org/10.1016/s0957-4166(03)00545-7.
Повний текст джерелаTakahashi, Masashi, and Osamu Kitagawa. "ChemInform Abstract: Catalytic Enantioselective Synthesis of Novel Atropisomeric Compounds Having an N-C Chiral Axis and Their Application to Asymmetric Reaction." ChemInform 43, no. 7 (January 23, 2012): no. http://dx.doi.org/10.1002/chin.201207241.
Повний текст джерелаMansour, Anissa, Yassin Belghith, Mohamed Salah Belkhiria, Anna Bujacz, Vincent Guérineau та Habib Nasri. "Synthesis, crystal structures and spectroscopic characterization of Co(II) bis(4,4′-bipyridine) with meso-porphyrins α,β,α,β-tetrakis(o-pivalamidophenyl) porphyrin (α,β,α,β-TpivPP) and tetraphenylporphyrin (TPP)". Journal of Porphyrins and Phthalocyanines 17, № 11 (листопад 2013): 1094–103. http://dx.doi.org/10.1142/s1088424613500843.
Повний текст джерелаFeng, Jia, and Ren-Rong Liu. "Catalytic Asymmetric Synthesis of N‐N Biaryl Atropisomers." Chemistry – A European Journal, October 18, 2023. http://dx.doi.org/10.1002/chem.202303165.
Повний текст джерелаLi, Tong, Linlin Shi, Xinhai Wang, Chen Yang, Dandan Yang, Mao-Ping Song, and Jun-Long Niu. "Cobalt-catalyzed atroposelective C−H activation/annulation to access N−N axially chiral frameworks." Nature Communications 14, no. 1 (August 29, 2023). http://dx.doi.org/10.1038/s41467-023-40978-4.
Повний текст джерелаCampbell, Aaron D. G., and Roly J. Armstrong. "Synthetic Strategies to Control C–N Atropisomerism in Acyclic Amines and Amides." Synthesis, February 21, 2023. http://dx.doi.org/10.1055/a-2039-5424.
Повний текст джерелаBiswas, Subhankar, Subham Kundu, and Subhas Chandra Pan. "Organocatalytic Asymmetric Synthesis of C‐N Atropisomers with Pyrrole, Oxindole and Succinimide Scaffold." Chemistry – An Asian Journal, November 10, 2024. http://dx.doi.org/10.1002/asia.202401132.
Повний текст джерелаZhang, Peng, Jia Feng, and Ren-Rong Liu. "Enantioselective Synthesis of Axially Chiral Benzimidazoles Bearing a C-N axis via Pd-Catalyzed Buchwald–Hartwig Amination." Synlett, April 25, 2022. http://dx.doi.org/10.1055/a-1833-8979.
Повний текст джерелаZhang, Peng, Jia Feng, and Ren-Rong Liu. "Enantioselective Synthesis of Axially Chiral Benzimidazoles Bearing a C-N axis via Pd-Catalyzed Buchwald–Hartwig Amination." Synlett, April 25, 2022. http://dx.doi.org/10.1055/a-1833-8979.
Повний текст джерелаRodríguez‐Salamanca, Patricia, Rosario Fernández, Valentín Hornillos, and José M. Lassaletta. "Asymmetric Synthesis of Axially Chiral C−N Atropisomers." Chemistry – A European Journal, March 25, 2022. http://dx.doi.org/10.1002/chem.202104442.
Повний текст джерелаWu, Chenggui, Ze‐Shui Liu, Yong Shang, Chang Liu, Shuang Deng, Hong‐Gang Cheng, Hengjiang Cong, Yinchun Jiao, and Qianghui Zhou. "Asymmetric Two‐component Alkenyl Catellani Reaction for the Construction of C–N Axial Chirality." Chinese Journal of Chemistry, November 29, 2023. http://dx.doi.org/10.1002/cjoc.202300621.
Повний текст джерелаZhan, Li-Wen, Chuan-Jun Lu, Jia Feng, and Ren-Rong Liu. "Atroposelective Synthesis of C‐N Vinylindole Atropisomers by Palladium‐Catalyzed Asymmetric Hydroarylation of 1‐Alkynylindoles." Angewandte Chemie, September 25, 2023. http://dx.doi.org/10.1002/ange.202312930.
Повний текст джерелаZhan, Li-Wen, Chuan-Jun Lu, Jia Feng, and Ren-Rong Liu. "Atroposelective Synthesis of C‐N Vinylindole Atropisomers by Palladium‐Catalyzed Asymmetric Hydroarylation of 1‐Alkynylindoles." Angewandte Chemie International Edition, September 25, 2023. http://dx.doi.org/10.1002/anie.202312930.
Повний текст джерелаShee, Sayan, Sowmya Shree Ranganathappa, Mahesh S. Gadhave, Romin Gogoi, and Akkattu T. Biju. "Enantioselective Synthesis of C‐O Axially Chiral Diaryl Ethers by NHC‐Catalyzed Atroposelective Desymmetrization." Angewandte Chemie International Edition, November 20, 2023. http://dx.doi.org/10.1002/anie.202311709.
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