Natural deep eutectic solvents as an efficient and reusable active system for the Nazarov cyclization

Stefano Nejrotti, Marta Iannicelli, Salwa Simona Jamil, Davide Arnodo, Marco Blangetti and Cristina Prandi

Green Chem., 2020, 22, 110
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A gold(i)-catalyzed substituent-controlled cycloisomerization of propargyl vinyl ethers to multi-substituted furofuran and furopyran derivatives

Yongxiang Liu, Shengfei Jin, Yanshi Wang, Shanshan Cui, Xiaoshi Peng, Yuanyuan Niu, Chuan Du and Maosheng Cheng

Chem. Commun., 2016, 52, 6233
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An allenylidene Au(i) catalyst derived from triazole units and its initial application

Bai-Ling Chen, Yuan Zhang, Ya-Ru Lei, Hui-Ming Wang and Zili Chen

Chem. Commun., 2020, 56, 5787
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Nazarov reaction: current trends and recent advances in the synthesis of natural compounds and their analogs

Maxim G. Vinogradov, Olga V. Turova and Sergei G. Zlotin

Org. Biomol. Chem., 2017, 15, 8245
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Nazarov cyclization of divinyl ketones bearing an ester group at the β-position: a remarkable effect of α-substitution and alkene geometry on regioselectivity

Gangarajula Sudhakar, Jakka Raghavaiah, Gaddam Mahesh and Kiran Kumar Singarapu

Org. Biomol. Chem., 2016, 14, 2866
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The synthesis of cycloalka[b]furans via an Au(i)-catalyzed tandem reaction of 3-yne-1,2-diols

Wei-Ting Liu, Zheng-Liang Xu, Xue-Qing Mou, Bang-Hong Zhang, Wen Bao, Shao-Hua Wang, Dongjun Lee, Lin-Sheng Lei and Kun Zhang

Org. Biomol. Chem., 2017, 15, 6333
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Computational insight into gold(i)-catalyzed intramolecular regioselectivity of tryptamine-ynamide cycloisomerizations

Shitao Sun, Jinle Hao, Maosheng Cheng, Yongxiang Liu and Bin Lin

Org. Biomol. Chem., 2023, 21, 2610
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Solvent strategy for unleashing the Lewis acidity of titanocene dichloride for rapid Mannich reactions

Ya Wu, Xiu Wang, Yanlong Luo, Jing Wang, Yajun Jian, Huaming Sun, Guofang Zhang, Weiqiang Zhang and Ziwei Gao

RSC Adv., 2016, 6, 15298
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Silver & gold-catalyzed routes to furans and benzofurans

Aurélien Blanc, Valérie Bénéteau, Jean-Marc Weibel and Patrick Pale

Org. Biomol. Chem., 2016, 14, 9184
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Overriding the alkynophilicity of gold: catalytic pathways from higher energy Au(i)–substrate complexes and reactant deactivation via unproductive complexation in the gold(i)-catalyzed propargyl Claisen rearrangement

Dinesh V. Vidhani, John W. Cran, Marie E. Krafft and Igor V. Alabugin

Org. Biomol. Chem., 2013, 11, 1624
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Exploring the gold mine: [Au]-catalysed transformations of enynals, enynones and enynols

A. Leela Siva Kumari, Alla Siva Reddy and K. C. Kumara Swamy

Org. Biomol. Chem., 2016, 14, 6651
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Sonogashira cross-coupling of 3-bromo-1,2-diones: an access to 3-alkynyl-1,2-diones

Anne Paju, Tõnis Kanger, Aleksander-Mati Müürisepp, Tiina Aid, Tõnis Pehk and Margus Lopp

Tetrahedron, 2014, 70, 5843
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Copper(I)-Catalyzed Heterocyclization of α-Acyl-α-alkynyl Ketene Dithioacetals: Synthesis of 3-Cyanofurans

Lianjie Wang, Xiaocui Liu, Mang Wang and Jun Liu

Org. Lett., 2016, 18, 2162
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Opposing Auxiliary Conformations Produce the Same Torquoselectivity in an Oxazolidinone-Directed Nazarov Cyclization

Bernard L. Flynn, Narasimhulu Manchala and Elizabeth H. Krenske

J. Am. Chem. Soc., 2013, 135, 9156
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Contiguous Quaternary Centers from a AuI‐Catalyzed Nazarov Cyclization

Jonathan Congmon and Marcus A. Tius

Eur J Org Chem, 2018, 2018, 2926
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Neutral Nazarov‐Type Cyclization Catalyzed by Palladium(0)

Naoyuki Shimada, Craig Stewart, William F. Bow, Anais Jolit, Kahoano Wong, Zhe Zhou and Marcus A. Tius

Angew Chem Int Ed, 2012, 51, 5727
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Flow Photo-Nazarov Reactions of 2-Furyl Vinyl Ketones: Cyclizing a Class of Traditionally Unreactive Heteroaromatic Enones

William L. Ashley, Evan L. Timpy and Thomas C. Coombs

J. Org. Chem., 2018, 83, 2516
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Electrophile-Induced Reactions of Cross-Conjugated Enynones in the Synthesis of Heterocycles

Alena S. Pankova

Chem Heterocycl Comp, 2020, 56, 829
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Total Synthesis of the Plant Growth Promoter Auxofuran Featuring a Gold(I) Catalyzed Furan Formation

Sibylle Riedel and Martin E. Maier

J. Org. Chem., 2020, 85, 8203
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Reagent Control of [1,2]‐Wagner–Meerwein Shift Chemoselectivity Following the Nazarov Cyclization: Application to the Total Synthesis of Enokipodin B

David Lebœuf, Christopher M. Wright and Alison J. Frontier

Chemistry A European J, 2013, 19, 4835
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Gold(III)-Catalyzed Intramolecular Cyclization of α-Pyrroles to Pyrrolopyridinones and Pyrroloazepinones: A DFT Study

Yang Li and Zhenyang Lin

Organometallics, 2015, 34, 3538
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Annulated N‐Heterocycles by Tandem Gold(I)‐Catalyzed [3,3]‐Rearrangement/Nazarov Reaction of Propargylic Ester Derivatives: an Experimental and Computational Study

Martina Petrović, Dina Scarpi, Béla Fiser, Enrique Gómez‐Bengoa and Ernesto G. Occhiato

Eur J Org Chem, 2015, 2015, 3943
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Gold(I)-Catalyzed Substitution-Controlled Syntheses of Spiro[indoline-3,3′-pyrrolidine] and Spiro[indoline-3,3′-piperidine] Derivatives

Jiang Zhu, Jiaji Li, Lianjie Zhang, Shitao Sun, Lu Yang, Jiayue Fu, Hanyang Sun, Maosheng Cheng, Bin Lin and Yongxiang Liu

J. Org. Chem., 2023, 88, 10586
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Neutral Nazarov‐Type Cyclization Catalyzed by Palladium(0)

Naoyuki Shimada, Craig Stewart, William F. Bow, Anais Jolit, Kahoano Wong, Zhe Zhou and Marcus A. Tius

Angewandte Chemie, 2012, 124, 5825
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ChemInform Abstract: Solvent Controlled Mechanistic Dichotomy in a Au(III)‐Catalyzed, Heterocyclization Triggered, Nazarov Reaction.

Marie E. Krafft, Dinesh V. Vidhani, John W. Cran and Mariappan Manoharan

ChemInform, 2011, 42
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Experimental and Theoretical Studies on the Nazarov Cyclization/Wagner–Meerwein Rearrangement Sequence

David Lebœuf, Vincent Gandon, Jennifer Ciesielski and Alison J. Frontier

J. Am. Chem. Soc., 2012, 134, 6296
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Tandem Brønsted Acid Promoted and Nazarov Carbocyclizations of Enyne Acetals to Hydroazulenones

Luz Escalante, Carlos González‐Rodríguez, Jesús A. Varela and Carlos Saá

Angewandte Chemie, 2012, 124, 12482
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Gold‐Catalyzed Cascade Reactions for Synthesis of Carbo‐ and Heterocycles: Selectivity and Diversity

Deyun Qian and Junliang Zhang

The Chemical Record, 2014, 14, 280
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It Is Not Just Up to the Substrate: Palladium(0) Cyclizes Nazarov Substrates through Intramolecular Allylic Alkylation

Tülay A. Ateşin, Gabriela M. Martinez and David Flores

Organometallics, 2017, 36, 3589
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Transition Metal-Mediated Synthesis of Monocyclic Aromatic Heterocycles

Anton V. Gulevich, Alexander S. Dudnik, Natalia Chernyak and Vladimir Gevorgyan

Chem. Rev., 2013, 113, 3084
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Access to Benzo[a]carbazoles and Indeno[1,2-c]quinolines by a Gold(I)-Catalyzed Tunable Domino Cyclization of Difunctional 1,2-Diphenylethynes

Xiaoshi Peng, Lifeng Zhu, Yuqian Hou, Yadong Pang, Yangming Li, Jiayue Fu, Lu Yang, Bin Lin, Yongxiang Liu and Maosheng Cheng

Org. Lett., 2017, 19, 3402
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Synthesis of Furans – Recent Advances

Ani Deepthi, Beneesh P. Babu and Aswathy L. Balachandran

Organic Preparations and Procedures International, 2019, 51, 409
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Origins of the Stereoselectivity in a Thiourea–Primary Amine-Catalyzed Nazarov Cyclization

Austin H. Asari, Yu-hong Lam, Marcus A. Tius and K. N. Houk

J. Am. Chem. Soc., 2015, 137, 13191
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Direct Synthesis of Functional Azaxanthones by Using a Domino Three-Component Reaction

Jianwei Yan, Ming Cheng, Feng Hu and Youhong Hu

Org. Lett., 2012, 14, 3206
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3-Alkyl-1,2-cyclopentanediones by Negishi cross-coupling of a 3-bromo-1,2-cyclopentanedione silyl enol ether with alkylzinc reagents: an approach to 2-substituted carboxylic acid γ-lactones, homocitric and lycoperdic acids

Anne Paju, Diana Kostomarova, Katharina Matkevitš, Marit Laos, Tõnis Pehk, Tõnis Kanger and Margus Lopp

Tetrahedron, 2015, 71, 9313
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Cationic Cyclizations and Rearrangements Promoted by a Heterogeneous Gold Catalyst

Tulaza Vaidya, Ryan Cheng, Peter N. Carlsen, Alison J. Frontier and Richard Eisenberg

Org. Lett., 2014, 16, 800
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Tandem Brønsted Acid Promoted and Nazarov Carbocyclizations of Enyne Acetals to Hydroazulenones

Luz Escalante, Carlos González‐Rodríguez, Jesús A. Varela and Carlos Saá

Angew Chem Int Ed, 2012, 51, 12316
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Formation of Four Different Aromatic Scaffolds from Nitriles through Tandem Divergent Catalysis

Ju Hyun Kim, Jean Bouffard and Sang‐gi Lee

Angewandte Chemie, 2014, 126, 6553
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Catalytic Nazarov Cyclization: The State of the Art

Tulaza Vaidya, Richard Eisenberg and Alison J. Frontier

ChemCatChem, 2011, 3, 1531
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Cyclisation Reactions Involving Alkyl Enol Ethers

Luisa Lempenauer, Gilles Lemière and Elisabet Duñach

Adv Synth Catal, 2019, 361, 5284
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Gold(I)/(III)-Catalyzed Rearrangement of Divinyl Ketones and Acyloxyalkynyloxiranes into Cyclopentenones

Marie Hoffmann, Jean-Marc Weibel, Pierre de Frémont, Patrick Pale and Aurélien Blanc

Org. Lett., 2014, 16, 908
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Gold-Catalyzed Reactions of Specially Activated Alkynes, Allenes, and Alkenes

Dominic Campeau, David F. León Rayo, Ali Mansour, Karim Muratov and Fabien Gagosz

Chem. Rev., 2021, 121, 8756
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Pentannulation of Heterocycles by Virtue of Precious Metal Catalysis

Martina Petrović and Ernesto G. Occhiato

Chemistry An Asian Journal, 2016, 11, 642
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Transition-Metal-Catalyzed Intramolecular Nucleophilic Addition of Carbonyl Groups to Alkynes

Lianfen Chen, Kai Chen and Shifa Zhu

Chem, 2018, 4, 1208
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Formation of Four Different Aromatic Scaffolds from Nitriles through Tandem Divergent Catalysis

Ju Hyun Kim, Jean Bouffard and Sang‐gi Lee

Angew Chem Int Ed, 2014, 53, 6435
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Mechanism of the Transition‐Metal‐Catalyzed Hydroarylation of Bromo‐Alkynes Revisited: Hydrogen versus Bromine Migration

Genping Huang, Bing Cheng, Liang Xu, Yahong Li and Yuanzhi Xia

Chemistry A European J, 2012, 18, 5401
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