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1. Full Text Development of Imino-[lambda]3-iodanes with Improved Reactivity for Metal-Free [2+2+1] Cycloaddition-Type Reactions
by Takafumi Baba and Shunsuke Takahashi and Yui Kambara and Akira Yoshimura and Victor N Nemykin and Viktor V Zhdankin and Akio Saito
Advanced synthesis & catalysis, ISSN 1615-4150, 11/2017, Volume 359, Issue 21, p. 3860
Cycloaddition
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2. Full Text Cycloaddition of Enamines with 1,4-Dimethoxy-2-butyne and 2-Butyne-1,4-diol Mediated by Titanium Tetrachloride
by Uludag, Nesimi and Yarapsanlı, Yesim and Asutay, Oktay and Gumus, Mustafa Kemal
Organic preparations and procedures international, ISSN 0030-4948, 07/2018, Volume 50, Issue 4, pp. 441 - 448
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3. Full Text Katalytisch-asymmetrische intramolekulare [4+2]-Cycloaddition von insitu generierten ortho-Chinonmethiden
by Youwei Xie and Benjamin List
Angewandte Chemie, ISSN 0044-8249, 04/2017, Volume 129, Issue 18, p. 5018
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4. Full Text Diversity-oriented synthesis of chromenopyrrolidines from azomethine ylides and 2-hydroxybenzylidene indandiones via base-controlled regiodivergent (3+2) cycloaddition
by Yu, Jhen-Kuei and Chien, Han-Wei and Lin, Yi-Jung and Karanam, Praneeth and Chen, Yu-Heng and Lin, Wenwei
Chemical communications (Cambridge, England), ISSN 1359-7345, 2018, Volume 54, Issue 71, pp. 9921 - 9924
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5. Full Text Fluorogenic iminosydnones: bioorthogonal tools for double turn-on click-and-release reactions (Electronic supplementary information (ESI) available. See DOI: 10.1039/d0cc03067h)
by Margaux Riomet and Karine Porte and Anne Wijkhuisen and Davide Audisio and Frédéric Taran
Chemical communications (Cambridge, England), ISSN 1359-7345, 01/2020, Volume 56, Issue 52, pp. 7183 - 7186
Cycloaddition
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6. Full Text 1,4-Additions of tricyclic 1,4-diphosphinines-a novel system to study σ-bond activation and π-π Dispersion interactions
by Koner, Abhishek and Kelemen, Zsolt and Schnakenburg, Gregor and Nyulászi, László and Streubel, Rainer
Chemical communications (Cambridge, England), ISSN 1359-7345, 2018, Volume 54, Issue 10, pp. 1182 - 1184
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7. Full Text The [4+2] cycloaddition of donor-acceptor cyclobutanes and nitrosoarenes
by Vemula, Naresh and Stevens, Andrew C and Schon, Tyler B and Pagenkopf, Brian L
Chemical communications (Cambridge, England), ISSN 1359-7345, 02/2014, Volume 50, Issue 14, pp. 1668 - 1670
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8. Full Text Efficient discovery of novel antimicrobials through integration of synthesis and testing in crude ribosome extract (Electronic supplementary information (ESI) available: Experimental procedures, characterization data, and additional spectra. See DOI: 10.1039/c9cc00144a)
by Zitai Sang and Yongping Lu and Yuanzheng Zhou and Yuan Ju and Qi An and Silan Shen and Jianyou Shi and Jun He and Tao Yang and Youfu Luo
Chemical communications (Cambridge, England), ISSN 1359-7345, 01/2019, Volume 55, Issue 42, pp. 5886 - 5889
Cycloaddition
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9. Full Text Kinetics studies of rapid strain-promoted [3+2] cycloadditions of nitrones with bicyclo[6.1.0]nonyne
by Mackenzie, Douglas A and Pezacki, John Paul
Canadian journal of chemistry, ISSN 0008-4042, 2014, Volume 92, Issue 4, pp. 337 - 340
strain-promoted alkyne−nitrone cycloaddition (SPANC) | cycloadditions bioorthogonales sans métal | metal-free bioothrogonal cycloadditions | click chemistry | bicyclo[6.1.0]nonyne | nitrones | cycloadditions 1,3-dipolaires | 1,3-dipolar cycloadditions | chimie « click | cycloaddition par catalyse forcée de nitrones à un alcyne (SPANC) | Nitrones | Strain-promoted alkyne-nitrone cycloaddition (SPANC) | Metal-free bioothrogonal cycloadditions | Click chemistry | Bicyclo[6.1.0]nonyne | Chemical reaction, Rate of | Chemical engineering | Nitrogen compounds | Research | Chemical properties | Ring formation (Chemistry) | Chemical engineering research | Identification and classification | Chemical reactions | Chemistry | Kinetics | Azides (organic) | Cycloaddition | Rate constants | Reaction kinetics | Labelling | Selectivity | Alkynes
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10. Full Text Conceptual, Qualitative, and Quantitative Theories of 1,3‐Dipolar and Diels–Alder Cycloadditions Used in Synthesis
by Ess, Daniel H and Jones, Gavin O and Houk, K. N
Advanced synthesis & catalysis, ISSN 1615-4150, 11/2006, Volume 348, Issue 16‐17, pp. 2337 - 2361
conceptual density functional theory | 1,3‐dipolar cycloadditions | hard and soft acid and base theory | configuration mixing | Diels–Alder cycloadditions | frontier molecular orbital theory | Conceptual density functional theory | Diels-Alder cycloadditions | 1,3-dipolar cycloadditions | Frontier molecular orbital theory | Configuration mixing | Hard and soft acid and base theory | Physical Sciences | Chemistry | Chemistry, Organic | Chemistry, Applied | Science & Technology
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11. Full Text Organocatalytic and metal-mediated asymmetric [3+2] cycloaddition reactions
by Xing, Yalan and Wang, Nai-Xing
Coordination chemistry reviews, ISSN 0010-8545, 06/2012, Volume 256, Issue 11-12, pp. 938 - 952
[3 + 2] cycloadditions | 1,3-Dipolar cycloaddition reactions | Asymmetric cycloadditions | Asymmetric catalysis | Organocatalysts | [3+2] cycloadditions | Physical Sciences | Chemistry, Inorganic & Nuclear | Chemistry | Science & Technology | Copper | Catalysis
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12. Full Text Organocatalytic Diastereo‐ and Enantioselective 1,3‐Dipolar Cycloaddition of Azlactones and Methyleneindolinones
by Sun, Wangsheng and Zhu, Gongming and Wu, Chongyang and Li, Guofeng and Hong, Liang and Wang, Rui
Angewandte Chemie (International ed.), ISSN 1433-7851, 08/2013, Volume 52, Issue 33, pp. 8633 - 8637
1,3‐dipolar cycloaddition | organocatalysis | asymmetric synthesis | methyleneindolinones | azlactones | 1,3-dipolar cycloaddition | Cyclization | Magnetic Resonance Spectroscopy | Stereoisomerism | Aza Compounds - chemistry | Molecular Structure | Catalysis | Cycloaddition Reaction | Indoles - chemistry | Spiro Compounds - chemistry | Lactones - chemistry | Enantiomers | Synthesis | Organic compounds | Index Medicus | Cycloaddition | Transformations | Ethers | Nuclei | Complexity
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13. Full Text Highly regiocontrolled and stereocontrolled syntheses of polysubstituted aminocyclohexanes: mild inverse-electron-demand Diels–Alder cycloadditions of electrophilic 2-pyridones
by Conyers, Ryan C and Mazzone, Jennifer R and Siegler, Maxime A and Posner, Gary H
Tetrahedron letters, ISSN 0040-4039, 07/2016, Volume 57, Issue 30, pp. 3344 - 3348
Gram scale 4+2 cycloadditions | Regiocontrolled and stereocontrolled cycloadditions | Inverse electron demand Diels–Alder cycloadditions
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