Artículos de revistas sobre el tema "Aryne Chemistry"
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Brown, Roger F. C. "Flash Vacuum Pyrolytic Generation of Arynes - in Retrospect". Australian Journal of Chemistry 63, n.º 7 (2010): 1002. http://dx.doi.org/10.1071/ch10086.
Texto completoLee, Daesung y Sourav Ghorai. "Aryne-Based Multicomponent Coupling Reactions". Synlett 31, n.º 08 (20 de marzo de 2020): 750–71. http://dx.doi.org/10.1055/s-0039-1690824.
Texto completoIdiris, Fahima I. M. y Christopher R. Jones. "Recent advances in fluoride-free aryne generation from arene precursors". Organic & Biomolecular Chemistry 15, n.º 43 (2017): 9044–56. http://dx.doi.org/10.1039/c7ob01947e.
Texto completoMartin, Nelson y Ruchi Bharti. "Arynes in Natural Product Synthesis". International Journal for Research in Applied Science and Engineering Technology 11, n.º 4 (30 de abril de 2023): 2633–44. http://dx.doi.org/10.22214/ijraset.2023.50703.
Texto completoNeog, Kashmiri y Pranjal Gogoi. "Recent advances in the synthesis of organophosphorus compounds via Kobayashi's aryne precursor: a review". Organic & Biomolecular Chemistry 18, n.º 47 (2020): 9549–61. http://dx.doi.org/10.1039/d0ob01988g.
Texto completoIto, Motoki, Yuka Yamabayashi, Mio Oikawa, Emi Kano, Kazuhiro Higuchi y Shigeo Sugiyama. "Silica gel-induced aryne generation from o-triazenylarylboronic acids as stable solid precursors". Organic Chemistry Frontiers 8, n.º 12 (2021): 2963–69. http://dx.doi.org/10.1039/d1qo00385b.
Texto completoTanaka, Hideya, Hitoshi Kuriki, Teruhiko Kubo, Itaru Osaka y Hiroto Yoshida. "Copper-catalyzed arylstannylation of arynes in a sequence". Chemical Communications 55, n.º 46 (2019): 6503–6. http://dx.doi.org/10.1039/c9cc02738f.
Texto completoNakajima, Hana, Yuki Hazama, Yuki Sakata, Keisuke Uchida, Takamitsu Hosoya y Suguru Yoshida. "Diverse diaryl sulfide synthesis through consecutive aryne reactions". Chemical Communications 57, n.º 21 (2021): 2621–24. http://dx.doi.org/10.1039/d0cc08373a.
Texto completoWenk, Hans Henning, Michael Winkler y Wolfram Sander. "One Century of Aryne Chemistry". Angewandte Chemie International Edition 42, n.º 5 (3 de febrero de 2003): 502–28. http://dx.doi.org/10.1002/anie.200390151.
Texto completoMhaske, Santosh y Ranjeet Dhokale. "Transition-Metal-Catalyzed Reactions Involving Arynes". Synthesis 50, n.º 01 (22 de noviembre de 2017): 1–16. http://dx.doi.org/10.1055/s-0036-1589517.
Texto completoSureshbabu, Popuri, Vinod Bhajammanavar, Venkata Surya Kumar Choutipalli, Venkatesan Subramanian y Mahiuddin Baidya. "Unorthodox cascade reaction of arynes and N-nitrosamides leading to indazole scaffolds". Chemical Communications 58, n.º 8 (2022): 1187–90. http://dx.doi.org/10.1039/d1cc05655g.
Texto completoSharma, Abhilash y Pranjal Gogoi. "Transition-metal free C(sp2)–C(sp2) bond formation: arylation of 4-aminocoumarins using arynes as an aryl source". Organic & Biomolecular Chemistry 17, n.º 40 (2019): 9014–25. http://dx.doi.org/10.1039/c9ob01919g.
Texto completoLi, Yang, Dachuan Qiu y Jiarong Shi. "Domino Aryne Precursor: A Step beyond the Boundary of Traditional Aryne Chemistry". Synlett 26, n.º 16 (9 de julio de 2015): 2194–98. http://dx.doi.org/10.1055/s-0034-1381041.
Texto completoUchida, Keisuke, Suguru Yoshida y Takamitsu Hosoya. "Synthetic Aryne Chemistry toward Multicomponent Coupling". Journal of Synthetic Organic Chemistry, Japan 77, n.º 2 (1 de febrero de 2019): 145–62. http://dx.doi.org/10.5059/yukigoseikyokaishi.77.145.
Texto completoCambie, RC, PI Higgs, PS Rutledge y PD Woodgate. "Aryne Chemistry of Podocarpic Acid Derivatives". Australian Journal of Chemistry 47, n.º 8 (1994): 1483. http://dx.doi.org/10.1071/ch9941483.
Texto completoSuh, Sung-Eun, Shuming Chen, K. N. Houk y David M. Chenoweth. "The mechanism of the triple aryne–tetrazine reaction cascade: theory and experiment". Chemical Science 9, n.º 39 (2018): 7688–93. http://dx.doi.org/10.1039/c8sc01796d.
Texto completoQiu, Dachuan, Jiarong Shi y Yang Li. "ChemInform Abstract: Domino Aryne Precursor: A Step Beyond the Boundary of Traditional Aryne Chemistry." ChemInform 47, n.º 7 (enero de 2016): no. http://dx.doi.org/10.1002/chin.201607155.
Texto completoMesgar, Milad, Justin Nguyen-Le y Olafs Daugulis. "1,2-Bis(arylthio)arene synthesis via aryne intermediates". Chemical Communications 55, n.º 64 (2019): 9467–70. http://dx.doi.org/10.1039/c9cc03863a.
Texto completoLi, Pan, Chunrui Wu, Jingjing Zhao, Yang Li, Weichao Xue y Feng Shi. "One-pot synthesis of dihydrobenzisoxazoles from hydroxylamines, acetylenedicarboxylates, and arynes via in situ generation of nitrones". Canadian Journal of Chemistry 91, n.º 1 (enero de 2013): 43–50. http://dx.doi.org/10.1139/cjc-2012-0199.
Texto completoXie, Chunsong, Leifang Liu, Yuhong Zhang y Peixin Xu. "Copper-Catalyzed Alkyne−Aryne and Alkyne−Alkene−Aryne Coupling Reactions". Organic Letters 10, n.º 12 (junio de 2008): 2393–96. http://dx.doi.org/10.1021/ol800651h.
Texto completoCAMBIE, R. C., P. I. HIGGS, P. S. RUTLEDGE y P. D. WOODGATE. "ChemInform Abstract: Aryne Chemistry of Podocarpic Acid Derivatives." ChemInform 25, n.º 52 (18 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199452212.
Texto completoLin, Yibei, Yali Chen, Xuyan Ma, Di Xu, Weiguo Cao y Jie Chen. "Aryne click chemistry: synthesis of oxadisilole fused benzotriazoles or naphthotriazoles from arynes and azides". Tetrahedron 67, n.º 5 (febrero de 2011): 856–59. http://dx.doi.org/10.1016/j.tet.2010.12.039.
Texto completoZilla, Mahesh K., Sheena Mahajan, Rajni Khajuria, Vivek K. Gupta, Kamal K. Kapoor y Asif Ali. "An efficient synthesis of 4-phenoxy-quinazoline, 2-phenoxy-quinoxaline, and 2-phenoxy-pyridine derivatives using aryne chemistry". RSC Advances 11, n.º 6 (2021): 3477–83. http://dx.doi.org/10.1039/d0ra09994e.
Texto completoShi, Jiarong, Yuanyuan Li y Yang Li. "Aryne multifunctionalization with benzdiyne and benztriyne equivalents". Chemical Society Reviews 46, n.º 6 (2017): 1707–19. http://dx.doi.org/10.1039/c6cs00694a.
Texto completoHu, Jinbo y Yuwen Zeng. "Bridging Fluorine and Aryne Chemistry: Vicinal Difunctionalization of Arynes Involving Nucleophilic Fluorination, Trifluoromethylation, or Trifluoromethylthiolation". Synthesis 48, n.º 14 (24 de mayo de 2016): 2137–50. http://dx.doi.org/10.1055/s-0035-1561641.
Texto completoHu, Jinbo y Yuwen Zeng. "Bridging Fluorine and Aryne Chemistry: Vicinal Difunctionalization of Arynes Involving Nucleophilic Fluorination, Trifluoromethylation, or Trifluoromethylthiolation". Synthesis 48, n.º 14 (4 de julio de 2016): e3-e3. http://dx.doi.org/10.1055/s-0035-1562547.
Texto completoSu, Shikuan, Jianxiong Li, Mingming Sun, Hongbin Zhao, Yali Chen y Jian Li. "A domino reaction of 2-isocyanophenyloxyacrylate and aryne to synthesize arenes with vicinal olefin and benzoxazole". Chemical Communications 54, n.º 69 (2018): 9611–14. http://dx.doi.org/10.1039/c8cc05735d.
Texto completoYoshida, Suguru y Takamitsu Hosoya. "The Renaissance and Bright Future of Synthetic Aryne Chemistry". Chemistry Letters 44, n.º 11 (5 de noviembre de 2015): 1450–60. http://dx.doi.org/10.1246/cl.150839.
Texto completoBennett, Martin A. "Aryne Complexes of Zerovalent Metals of the Nickel Triad". Australian Journal of Chemistry 63, n.º 7 (2010): 1066. http://dx.doi.org/10.1071/ch10198.
Texto completoGupta, Saswata, Yongjia Lin, Yuanzhi Xia, Donald J. Wink y Daesung Lee. "Alder-ene reactions driven by high steric strain and bond angle distortion to form benzocyclobutenes". Chemical Science 10, n.º 7 (2019): 2212–17. http://dx.doi.org/10.1039/c8sc04277b.
Texto completoMatsuzawa, Tsubasa, Takamitsu Hosoya y Suguru Yoshida. "One-step synthesis of benzo[b]thiophenes by aryne reaction with alkynyl sulfides". Chemical Science 11, n.º 35 (2020): 9691–96. http://dx.doi.org/10.1039/d0sc04450d.
Texto completoCrump, Stephen L., Jill Netka y Bruce Rickborn. "Preparation of isobenzofuran-aryne cycloadducts". Journal of Organic Chemistry 50, n.º 15 (julio de 1985): 2746–50. http://dx.doi.org/10.1021/jo00215a031.
Texto completoPollart, Daniel J. y Bruce Rickborn. "Regioselectivity of alkoxyisobenzofuran-aryne cycloadditions". Journal of Organic Chemistry 52, n.º 5 (marzo de 1987): 792–98. http://dx.doi.org/10.1021/jo00381a016.
Texto completoLin, Yibei, Yali Chen, Xuyan Ma, Di Xu, Weiguo Cao y Jie Chen. "ChemInform Abstract: Aryne Click Chemistry: Synthesis of Oxadisilole Fused Benzotriazoles or Naphthotriazoles from Arynes and Azides." ChemInform 42, n.º 27 (9 de junio de 2011): no. http://dx.doi.org/10.1002/chin.201127025.
Texto completoJones, Christopher, Weitao Sun, Piera Trinchera, Nada Kurdi, David Palomas, Rachel Crespo-Otero, Saeed Afshinjavid y Farideh Javid. "Aryne-Mediated Arylation of Hantzsch Esters: Access to Highly Substituted Aryl-dihydropyridines, Aryl-tetrahydropyridines and Spiro[benzocyclobutene-1,1′-(3′,4′-dihydropyridines)]". Synthesis 50, n.º 23 (25 de octubre de 2018): 4591–605. http://dx.doi.org/10.1055/s-0037-1611065.
Texto completoRoy, Tony, Manikandan Thangaraj, Trinadh Kaicharla, Rupa V. Kamath, Rajesh G. Gonnade y Akkattu T. Biju. "The Aryne [2,3] Stevens Rearrangement". Organic Letters 18, n.º 20 (13 de octubre de 2016): 5428–31. http://dx.doi.org/10.1021/acs.orglett.6b02809.
Texto completoLi, Bingnan, Shaoyu Mai y Qiuling Song. "Synthesis of fused benzimidazoles via successive nucleophilic additions of benzimidazole derivatives to arynes under transition metal-free conditions". Organic Chemistry Frontiers 5, n.º 10 (2018): 1639–42. http://dx.doi.org/10.1039/c8qo00251g.
Texto completoSanz, Roberto. "RECENT APPLICATIONS OF ARYNE CHEMISTRY TO ORGANIC SYNTHESIS. A REVIEW". Organic Preparations and Procedures International 40, n.º 3 (junio de 2008): 215–91. http://dx.doi.org/10.1080/00304940809458089.
Texto completoWu, Chunrui y Feng Shi. "A Closer Look at Aryne Chemistry: Details that Remain Mysterious". Asian Journal of Organic Chemistry 2, n.º 2 (17 de enero de 2013): 116–25. http://dx.doi.org/10.1002/ajoc.201200142.
Texto completoTan, Jiajing, Binbin Liu y Shuaisong Su. "Aryne triggered dearomatization reaction of isoquinolines and quinolines with chloroform". Organic Chemistry Frontiers 5, n.º 21 (2018): 3093–97. http://dx.doi.org/10.1039/c8qo00838h.
Texto completoNeog, Kashmiri, Dhiraj Dutta, Babulal Das y Pranjal Gogoi. "Aryne insertion into the PO bond: one-pot synthesis of quaternary phosphonium triflates". Organic & Biomolecular Chemistry 17, n.º 26 (2019): 6450–60. http://dx.doi.org/10.1039/c9ob01157a.
Texto completoRahman, Matiur, Avik Kumar Bagdi, Dmitry S. Kopchuk, Igor S. Kovalev, Grigory V. Zyryanov, Oleg N. Chupakhin, Adinath Majee y Alakananda Hajra. "Recent advances in the synthesis of fluorinated compounds via an aryne intermediate". Organic & Biomolecular Chemistry 18, n.º 47 (2020): 9562–82. http://dx.doi.org/10.1039/d0ob01638a.
Texto completoPan, Xuan, Yantao Ma y Zhanzhu Liu. "A concise synthesis of (E)-3-aryl-2,3,4,5-tetrahydro-1H-3-benzazonines by aryne induced [2,3] Stevens rearrangement of 1,2,3,4-tetrahydroisoquinolines". Organic & Biomolecular Chemistry 16, n.º 40 (2018): 7393–99. http://dx.doi.org/10.1039/c8ob02099j.
Texto completoHazarika, Hemanta, Kangkana Chutia, Babulal Das y Pranjal Gogoi. "One-pot synthesis of 3-substituted-3-hydroxyindolin-2-ones: three component coupling of N-protected isatin, aryne precursor and 1,3-cyclodione under metal-free conditions". New Journal of Chemistry 46, n.º 1 (2022): 86–96. http://dx.doi.org/10.1039/d1nj04295e.
Texto completoMeerakrishna, Ramakrishnan Suseela, Suresh Snoxma Smile, Mohanakumaran Athira, Venkata Surya Kumar Choutipalli y Ponnusamy Shanmugam. "Diverse reactivity of isatin-based N,N′-cyclic azomethine imine dipoles with arynes: synthesis of 1′-methyl-2′-oxospiro [indene-1,3′-indolines] and 3-aryl-3-pyrazol-2-oxindoles". New Journal of Chemistry 44, n.º 27 (2020): 11593–601. http://dx.doi.org/10.1039/d0nj01684e.
Texto completoVenkatesh, Telugu, Prathama S. Mainkar y Srivari Chandrasekhar. "Total synthesis of (±)-galanthamine from GABA through regioselective aryne insertion". Organic & Biomolecular Chemistry 17, n.º 8 (2019): 2192–98. http://dx.doi.org/10.1039/c8ob03123a.
Texto completoPavlyuk, D. E., S. Gundala, I. S. Kovalev, D. S. Kopchuk, A. P. Krinochkin, A. V. Budeev, G. V. Zyryanov, P. Venkatapuram, V. L. Rusinov y O. N. Chupakhin. "Reactions of Perylene with Aryne Intermediates". Russian Journal of Organic Chemistry 55, n.º 3 (marzo de 2019): 409–11. http://dx.doi.org/10.1134/s1070428019030278.
Texto completoPayili, Nagaraju, Santhosh Reddy Rekula, Anjaiah Aitha, V. V. S. R. N. Anji Karun Mutha, Challa Gangu Naidu y Satyanarayana Yennam. "Synthesis of dibenzo[a,d]cycloheptanoids via aryne insertion into 2-arylidene-1,3-indandiones". Organic & Biomolecular Chemistry 17, n.º 43 (2019): 9442–46. http://dx.doi.org/10.1039/c9ob01900f.
Texto completoHazarika, Hemanta y Pranjal Gogoi. "Direct synthesis of ortho-methylthio allyl and vinyl ethers via three component reaction of aryne, activated alkene and DMSO". Organic & Biomolecular Chemistry 18, n.º 14 (2020): 2727–38. http://dx.doi.org/10.1039/d0ob00275e.
Texto completoWinkler, Michael y Wolfram Sander. "Matrix Isolation and Electronic Structure of Di- and Tridehydrobenzenes". Australian Journal of Chemistry 63, n.º 7 (2010): 1013. http://dx.doi.org/10.1071/ch10113.
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