Access the full text.
Sign up today, get DeepDyve free for 14 days.
M. Hesse (2002)
Alkaloids: nature's curse or blessing?
V. Mamane (2017)
Cascade Reactions Involving Aromatic N-Heterocycles: C-N Bond Formation as Key-step Towards the Synthesis of N-fused Polycyclic HeterocyclesCurrent Organic Chemistry, 21
B. Liu, Fangyun Hu, Bing‐Feng Shi (2014)
Synthesis of Sterically Congested Polycyclic Aromatic Hydrocarbons: Rhodium(III)-Catalyzed Cascade Oxidative Annulation of Aryl Ketoximes with Diphenylacetylene by Sequential Cleavage of Multiple CH BondsAdvanced Synthesis & Catalysis, 356
Julia-Christina Wasilke, S. Obrey, R. Baker, G. Bazan (2005)
Concurrent tandem catalysis.Chemical reviews, 105 3
Sumit Kumar, Amandeep Singh, K. Kumar, Vipan Kumar (2017)
Recent insights into synthetic β-carbolines with anti-cancer activities.European journal of medicinal chemistry, 142
Xuefeng Xu, Yurong Yang, Xin Chen, Xu Zhang, Wei Yi (2017)
The one-pot synthesis of quinolines via Co(iii)-catalyzed C-H activation/carbonylation/cyclization of anilines.Organic & biomolecular chemistry, 15 43
Ren-Hong Chen, Sunliang Cui (2017)
Rh(III)-Catalyzed C-H Activation/Cyclization of Benzamides and Diazonaphthalen-2(1H)-ones for Synthesis of Lactones.Organic letters, 19 15
R. Shang, L. Ilies, E. Nakamura (2017)
Iron-Catalyzed C-H Bond Activation.Chemical reviews, 117 13
Xuefeng Xu, Yurong Yang, Xu Zhang, Wei Yi (2018)
Direct Synthesis of Quinolines via Co(III)-Catalyzed and DMSO-Involved C-H Activation/Cyclization of Anilines with Alkynes.Organic letters, 20 3
P. Kalck, M. Urrutigoïty (2018)
Tandem Hydroaminomethylation Reaction to Synthesize Amines from Alkenes.Chemical reviews, 118 7
V. Yadav, K. Srivastava, R. Tripathi, S. Batra (2017)
Synthesis of β-carboline-fused 1,4-oxazepines and their assessment as antiplasmodial agentsTetrahedron, 73
Yanni Li, Yu-Ching Chang, Yufen Li, Cheng Cao, Jinshuang Yang, Baoling Wang, Deqiang Liang (2018)
Iron‐Catalyzed exo‐Selective Synthesis of Cyanoalkyl Indolines via Cyanoisopropylarylation of Unactivated AlkenesAdvanced Synthesis & Catalysis, 360
R. Nallagonda, N. Thrimurtulu, Chandra Volla (2018)
Cobalt-Catalyzed Diastereoselective [4+2] Annulation of Phosphinamides with Heterobicyclic Alkenes at Room TemperatureAdvanced Synthesis & Catalysis, 360
Ching-Zong Luo, Jayachandran Jayakumar, Parthasarathy Gandeepan, Yunxiang Wu, Chien‐Hong Cheng (2015)
Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.Organic letters, 17 4
Tingman Wang, Di Zhang, Wei‐Wei Liao (2018)
Versatile synthesis of functionalized β- and γ-carbolines via Pd-catalyzed C-H addition to nitriles/cyclization sequences.Chemical communications, 54 16
Qiyi Yao, Lingkai Kong, Fangfang Zhang, Tao Xianghua, Yanzhong Li (2017)
Base‐Promoted Tandem Reaction towards Conjugated Dienone or Chromone Derivatives with a Cyano Group: Insertion of Alkynes into C–C σ‐Bonds of 3‐OxopropanenitrilesAdvanced Synthesis & Catalysis, 359
R. Alekseyev, A. Kurkin, M. Yurovskaya (2009)
γ-Carbolines and their hydrogenated derivatives. 1. Aromatic γ-carbolines: methods of synthesis, chemical and biological properties (review)Chemistry of Heterocyclic Compounds, 45
Zhenghua Li, Liangliang Song, L. Meervelt, Guilong Tian, E. Eycken (2018)
Cationic Gold(I)-Catalyzed Cascade Bicyclizations for Divergent Synthesis of (Spiro)polyheterocyclesACS Catalysis
Yidong Wang, Peichao Zhang, Xiaoyu Di, Q. Dai, Zhanming Zhang, Junliang Zhang (2017)
Gold-Catalyzed Asymmetric Intramolecular Cyclization of N-Allenamides for the Synthesis of Chiral Tetrahydrocarbolines.Angewandte Chemie, 56 50
Mingliang Li, F. Kwong (2018)
Titelbild: Cobalt‐Catalyzed Tandem C−H Activation/C−C Cleavage/C−H Cyclization of Aromatic Amides with Alkylidenecyclopropanes (Angew. Chem. 22/2018)Angewandte Chemie, 130
N. Senthilkumar, Parthasarathy Gandeepan, Jayachandran Jayakumar, Chien‐Hong Cheng (2014)
Rh(III)-catalyzed synthesis of 1-substituted isoquinolinium salts via a C-H bond activation reaction of ketimines with alkynes.Chemical communications, 50 23
Jintao Xia, Zhipeng Huang, Xukai Zhou, Xifa Yang, Feng Wang, Xingwei Li (2018)
Rh(III)-Catalyzed Acceptorless Dehydrogenative Coupling of (Hetero)arenes with 2-Carboxyl Allylic Alcohols.Organic letters, 20 3
Wei Zhang, Cheng-Qi Wang, Hui Lin, Lin Dong, Yan-Jun Xu (2016)
Synthesis of Mesoionic Isoquinolines by Rhodium(III)-Catalyzed C-H Activation.Chemistry, 22 3
Tyler Saint-Denis, Ru-Yi Zhu, Gang Chen, Qing-Feng Wu, jin-quan yu (2018)
Enantioselective C(sp3)‒H bond activation by chiral transition metal catalystsScience, 359
Shangze Wu, Xiaoyan Wu, C. Fu, Shengming Ma (2018)
Rhodium(III)-Catalyzed C-H Functionalization in Water for Isoindolin-1-one Synthesis.Organic letters, 20 10
Beatriz Abarca, Raúl Custodio, A. Cuadro, David Sucunza, A. Domingo, F. Mendicuti, J. Alvarez-Builla, J. Vaquero (2014)
Efficient synthesis of an indoloquinolizinium alkaloid selective DNA-binder by ring-closing metathesis.Organic letters, 16 13
C. Esteves, Peter Smith, T. Donohoe (2017)
Catalytic Enolate Arylation with 3-Bromoindoles Allows the Formation of β-Carbolines.The Journal of organic chemistry, 82 8
Zhe Dong, Zhihui Ren, S. Thompson, Yan Xu, Guangbin Dong (2017)
Transition-Metal-Catalyzed C-H Alkylation Using Alkenes.Chemical reviews, 117 13
Yudong Yang, Jingbo Lan, J. You (2017)
Oxidative C-H/C-H Coupling Reactions between Two (Hetero)arenes.Chemical reviews, 117 13
Ju Kim, Y. Ko, J. Bouffard, Sang-gi Lee (2015)
Advances in tandem reactions with organozinc reagents.Chemical Society reviews, 44 8
Ling Li, W. Brennessel, W. Jones (2008)
An efficient low-temperature route to polycyclic isoquinoline salt synthesis via C-H activation with [Cp*MCl2]2 (M = Rh, Ir).Journal of the American Chemical Society, 130 37
M. Lounasmaa, P. Hanhinen, Minna Westersund, Née Halonen (1999)
Chapter 2 – The Sarpagine Group of Indole AlkaloidsThe Alkaloids: Chemistry and Biology, 52
Kenji Sugimoto, Y. Matsuya (2017)
Recent applications of gold-catalyzed cascade reactions in total synthesis of natural productTetrahedron Letters, 58
Borbála Bogányi, J. Kámán (2013)
A concise synthesis of indoloquinoline skeletons applying two consecutive Pd-catalyzed reactionsTetrahedron, 69
Chao‐Zheng Zhou, Feifei Fang, Yilang Cheng, Yazhou Li, Hong Liu, Yu Zhou (2018)
Rhodium(III)‐Catalyzed C‐H Activation of Benzoylacetonitriles and Cyclization with Sulfoxonium Ylides to NaphtholsAdvanced Synthesis & Catalysis, 360
R. Woodward, B. Witkop (1949)
The structure of sempervirine.Journal of the American Chemical Society, 71 1
Xiai Luo, Yankun Xu, Genhua Xiao, Wenjuan Liu, C. Qian, Guobo Deng, Jianxin Song, Yun Liang, Chunming Yang (2018)
Palladium-Catalyzed Tandem Reaction of Three Aryl Iodides Involving Triple C-H Activation.Organic letters, 20 10
H. Cui, Jing-Fang Wang, Haipin Zhou, Xiao-Lin You, Xiaolan Jiang (2017)
Catalyst-free synthesis of novel dimeric β-carboline derivatives via an unexpected [2 + 2 + 2] annulation.Organic & biomolecular chemistry, 15 18
Wanchun Gong, Zhi Zhou, Jingjing Shi, Bo Wu, Biyun Huang, Wei Yi (2018)
Catalyst-Controlled [3 + 2] and [4 + 2] Annulations of Oximes with Propargyl Alcohols: Divergent Access to Indenamines and Isoquinolines.Organic letters, 20 1
Daria Grosheva, N. Cramer (2017)
Ketene Aminal Phosphates: Competent Substrates for Enantioselective Pd(0)-Catalyzed C-H FunctionalizationsACS Catalysis, 7
Prajesh Volvoikar, S. Tilve (2016)
Iodine-Mediated Intramolecular Dehydrogenative Coupling: Synthesis of N-Alkylindolo[3,2-c]- and -[2,3-c]quinoline Iodides.Organic letters, 18 5
Jayachandran Jayakumar, K. Parthasarathy, Chien‐Hong Cheng (2012)
One-pot synthesis of isoquinolinium salts by rhodium-catalyzed C-H bond activation: application to the total synthesis of oxychelerythrine.Angewandte Chemie, 51 1
S. Miert, Steven Hostyn, B. Maes, K. Cimanga, R. Brun, M. Kaiser, P. Mátyus, R. Dommisse, G. Lemiére, A. Vlietinck, L. Pieters (2005)
Isoneocryptolepine, a synthetic indoloquinoline alkaloid, as an antiplasmodial lead compound.Journal of natural products, 68 5
Ching-Zong Luo, Parthasarathy Gandeepan, Chien‐Hong Cheng (2013)
A convenient synthesis of quinolizinium salts through Rh(III) or Ru(II)-catalyzed C-H bond activation of 2-alkenylpyridines.Chemical communications, 49 76
Junbin Tang, Shiqing Li, Zheng Liu, Yinsong Zhao, Zhijie She, Vilas Kadam, G. Gao, Jingbo Lan, J. You (2017)
Cascade C-H Annulation of Aldoximes with Alkynes Using O2 as the Sole Oxidant: One-Pot Access to Multisubstituted Protoberberine Skeletons.Organic letters, 19 3
Xiaohong Pan, Chunying Yang, J. Cleveland, T. Bannister (2016)
Synthesis and Cytoxicity of Sempervirine and Analogues.The Journal of organic chemistry, 81 5
Liang Yi, Yuyang Zhang, Zhao-Fei Zhang, Dequn Sun, Song Ye (2017)
Synthesis of Dihydropyridinone-Fused Indoles and α-Carbolines via N-Heterocyclic Carbene-Catalyzed [3 + 3] Annulation of Indolin-2-imines and Bromoenals.Organic letters, 19 9
Steven Hostyn, B. Maes, L. Pieters, G. Lemiére, P. Mátyus, G. Hajos, R. Dommisse (2005)
Synthesis of the benzo-β-carboline isoneocryptolepine: the missing indoloquinoline isomer in the alkaloid series cryptolepine, neocryptolepine and isocryptolepineTetrahedron, 61
H. Pellissier (2013)
Stereocontrolled domino reactions.Chemical reviews, 113 1
Xiaohong Pan, T. Bannister (2014)
Sequential Sonagashira and Larock Indole Synthesis Reactions in a General Strategy To Prepare Biologically Active β-Carboline-Containing AlkaloidsOrganic Letters, 16
C. Bradsher, E. Litzinger (1964)
A New Route to the 13H-Indolo[2,3-a]a cridizinium System1Journal of Organic Chemistry, 29
Kirk Shimkin, J. Montgomery (2018)
Synthesis of Tetrasubstituted Alkenes by Tandem Metallacycle Formation/Cross-Electrophile Coupling.Journal of the American Chemical Society, 140 23
R. Cao, W. Peng, Zihou Wang, A. Xu (2007)
β-Carboline Alkaloids: Biochemical and Pharmacological FunctionsCurrent Medicinal Chemistry, 14
Mingming Zhang, Dianqing Sun (2015)
Recent Advances of Natural and Synthetic β-Carbolines as Anticancer Agents.Anti-cancer agents in medicinal chemistry, 15 5
Chandra Volla, Iuliana Atodiresei, M. Rueping (2014)
Catalytic C-C bond-forming multi-component cascade or domino reactions: pushing the boundaries of complexity in asymmetric organocatalysis.Chemical reviews, 114 4
Mingliang Li, F. Kwong (2018)
Cover Picture: Cobalt‐Catalyzed Tandem C−H Activation/C−C Cleavage/C−H Cyclization of Aromatic Amides with Alkylidenecyclopropanes (Angew. Chem. Int. Ed. 22/2018)Angewandte Chemie International Edition
Ching-Zong Luo, Parthasarathy Gandeepan, Jayachandran Jayakumar, K. Parthasarathy, Yu-wei Chang, Chien‐Hong Cheng (2013)
Rh(III) -catalyzed C-H activation: a versatile route towards various polycyclic pyridinium salts.Chemistry, 19 42
G. Viola, F. Dall'acqua, N. Gabellini, S. Moro, D. Vedaldi, H. Ihmels (2002)
Indolo[2,3‐b]‐Quinolizinium Bromide: An Efficient Intercalator with DNA‐Photodamaging PropertiesChemBioChem, 3
G. Cera, M. Lanzi, D. Balestri, Nicola Ca’, R. Maggi, F. Bigi, M. Malacria, G. Maestri (2018)
Synthesis of Carbolines via Palladium/Carboxylic Acid Joint Catalysis.Organic letters, 20 11
Zhuo Wang, Tongyu Li, Siyang Xing, Bolin Zhu (2018)
Facile and practical synthesis of β-carbolinium salts and γ-carbolinium salts via rhodium-catalyzed three-component reactions.Organic & biomolecular chemistry, 16 27
Guoying Zhang, Lei Yang, Yanyu Wang, Yinjun Xie, Hanmin Huang (2013)
An efficient Rh/O2 catalytic system for oxidative C-H activation/annulation: evidence for Rh(I) to Rh(III) oxidation by molecular oxygen.Journal of the American Chemical Society, 135 24
K. Parthasarathy, N. Senthilkumar, Jayachandran Jayakumar, Chien‐Hong Cheng (2012)
Ru(II)-catalyzed C-H bond activation for the synthesis of substituted isoquinolinium salts from benzaldehydes, amines, and alkynes.Organic letters, 14 13
P. Srihari, B. Padmabhavani, S. Ramesh, Y. Kumar, Ashita Singh, R. Ummanni (2015)
PMA-SiO2 catalyzed synthesis of indolo[2,3-c]quinolines as potent anti cancer agents.Bioorganic & medicinal chemistry letters, 25 11
Ravi Chinnagolla, Sandeep Pimparkar, M. Jeganmohan (2012)
Ruthenium-catalyzed highly regioselective cyclization of ketoximes with alkynes by C-H bond activation: a practical route to synthesize substituted isoquinolines.Organic letters, 14 12
(2016)
Spotlights on our sister journals: Eur. J. Org. Chem. 5/2016
N. Mishra, Satyasheel Sharma, Jihye Park, S. Han, I. Kim (2017)
Recent Advances in Catalytic C(sp2)–H Allylation ReactionsACS Catalysis, 7
Hong Yi, Guoting Zhang, Huamin Wang, Zhiyuan Huang, Jue Wang, A. Singh, A. Lei (2017)
Recent Advances in Radical C-H Activation/Radical Cross-Coupling.Chemical reviews, 117 13
M. Kapoor, Daniel Liu, M. Young (2018)
Carbon Dioxide-Mediated C(sp3)-H Arylation of Amine Substrates.Journal of the American Chemical Society, 140 22
E. Tan, Ophélie Quinonero, M. Orbe, A. Echavarren (2018)
Broad-Scope Rh-Catalyzed Inverse-Sonogashira Reaction Directed by Weakly Coordinating GroupsACS Catalysis, 8
Shi Tang, Jian Wang, Zhuang Xiong, Zeqiang Xie, Dengke Li, Jinbo Huang, Qiang Zhu (2017)
Palladium-Catalyzed Imidoylative Cyclization of Tryptophan-Derived Isocyanides: Access to β-Carbolines.Organic letters, 19 20
A [Cp*RhCl2]2‐catalyzed tandem reaction of indolyl aldehydes, amines, and alkynes featuring the formation of two C−C bonds, two C−N bonds, and one C=N bond is described. This strategy involves double C−H activation and double insertion of alkynes, furnishing a series of pentacyclic carboline‐containing salts in good yields under mild conditions. It provides a good choice for rapidly constructing libraries of such pentacyclic carboline‐containing salts.
Asian Journal of Organic Chemistry – Wiley
Published: Jan 1, 2019
Keywords: ; ; ; ;
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.