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Journal articles on the topic 'Aminofuranos'

Author: Grafiati

Published: 4 June 2021

Last updated: 14 February 2022

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1

Cheng, Xing, Yinghua Yu, Zhifeng Mao, Jianxin Chen, and Xueliang Huang. "Facile synthesis of substituted 3-aminofurans through a tandem reaction of N-sulfonyl-1,2,3-triazoles with propargyl alcohols." Organic & Biomolecular Chemistry 14, no. 16 (2016): 3878–82. http://dx.doi.org/10.1039/c6ob00377j.

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2

Guguloth, Veeranna, Ramesh Balaboina, Narasimha Swamy Thirukovela, and Ravinder Vadde. "One-pot synthesis of 3-aminofurans using a simple and efficient recyclable CuI/[bmim]PF6 system." Organic & Biomolecular Chemistry 19, no. 34 (2021): 7438–45. http://dx.doi.org/10.1039/d1ob01132d.

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3

P., Rajesh, Abdulrahman I. Almansour, Natarajan Arumugam, and Srinivasarao Yaragorla. "Calcium-catalyzed formal [3 + 2] annulation of C,N-diacyliminium ions with nucleophilic phenols: a diversity oriented synthesis of 3-aminofurans." Organic & Biomolecular Chemistry 19, no. 5 (2021): 1060–65. http://dx.doi.org/10.1039/d0ob02276d.

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We report a one-pot, three-component, solvent-free, cascade reaction for the synthesis of 3-aminofurans using a calcium catalyst, in which, the in situ formed C,N-diacyliminium ion, is the key intermediate.

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4

Lingham, Anthony R., Helmut M. Hügel, and Trevor J. Rook. "Diels - Alder Reactions of 3-Furylamines in Organic and Aqueous Solvents." Australian Journal of Chemistry 59, no. 5 (2006): 336. http://dx.doi.org/10.1071/ch05339.

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Various 5-methyl-3-aminofurans have been shown to undergo facile Diels–Alder reactions with methyl acrylate in aqueous media. Reactions proceeded with exclusive regiochemistry, and enamine cycloadducts were readily hydrolyzed to afford 7-oxabicyclo[2.2.1]heptanones in high yields.

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5

Lythgoe, David J., Ian Mcclenaghan, and Christopher A. Ramsden. "A study of 2-aminofurans." Journal of Heterocyclic Chemistry 30, no. 1 (1993): 113–17. http://dx.doi.org/10.1002/jhet.5570300120.

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6

Anary-Abbasinejad, M., M. Mosslemin, and H. Anaraki-Ardakani. "Multicomponent Synthesis of 2-Aminofurans." Synfacts 2009, no. 12 (2009): 1326. http://dx.doi.org/10.1055/s-0029-1218222.

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7

Ivanov, D. V., and N. M. Igidov. "SYNTHESIS OF SUBSTITUTED 2-AMINOFURANS (REVIEW)." Вестник Пермского университета. Серия «Химия» = Bulletin of Perm University. CHEMISTRY 8, no. 2 (2018): 197–209. http://dx.doi.org/10.17072/2223-1838-2018-2-197-209.

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8

Yavari, Issa, Hoorieh Djahaniani, and Loghman Moradi. "Synthesis of highly functionalised 2-aminofurans." Mendeleev Communications 14, no. 1 (2004): 38–39. http://dx.doi.org/10.1070/mc2004v014n01abeh001860.

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9

Bornadiego, Ana, Jesús Díaz, and Carlos F. Marcos. "Tandem synthesis of 4-aminoxanthones is controlled by a water-assisted tautomerization: a general straightforward reaction." Organic & Biomolecular Chemistry 17, no. 6 (2019): 1410–22. http://dx.doi.org/10.1039/c8ob02527d.

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10

Largeron, Martine, and Maurice-Bernard Fleury. "Electrochemical synthesis of 2-substituted 5-aminofurans." Tetrahedron Letters 32, no. 5 (1991): 631–34. http://dx.doi.org/10.1016/s0040-4039(00)74846-5.

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11

Huynh, Thi Ngoc Tram, Pascal Retailleau, Clément Denhez, Kim Phi Phung Nguyen, and Dom Guillaume. "Regioselective synthesis of 3,4,5-trisubstituted 2-aminofurans." Org. Biomol. Chem. 12, no. 28 (2014): 5098–101. http://dx.doi.org/10.1039/c4ob01037j.

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Three series of methyl 5-substituted 2-aminofuran-4-keto-3-carboxylates have been prepared following a multicomponent reaction strategy by the addition of an isocyanide to 4-oxo-2-butynoate in the presence of an aldehyde.

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12

LYTHGOE, D. J., I. MCCLENAGHAN, and C. A. RAMSDEN. "ChemInform Abstract: A Study of 2-Aminofurans." ChemInform 24, no. 34 (2010): no. http://dx.doi.org/10.1002/chin.199334152.

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13

Shoji, Taku, Nanami Iida, Akari Yamazaki, et al. "Synthesis of phthalimides cross-conjugated with an azulene ring, and their structural, optical and electrochemical properties." Organic & Biomolecular Chemistry 18, no. 12 (2020): 2274–82. http://dx.doi.org/10.1039/d0ob00164c.

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14

Mal, Dipakranjan, Supriti Jana, and Mausumi Bandyopadhyay. "Regioselective Synthesis of Dihydro-1H-furo[b]indol-1-ones and Their Carbanionic Reactivity." Synthesis 50, no. 18 (2018): 3723–30. http://dx.doi.org/10.1055/s-0037-1610439.

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A general synthesis of 3,4-dihydro-1H-furo[b]indol-1-ones, representing a furanone-fused pyrrole unit, has been developed. The dehydrohalogenative cyclization of 4-aminofuranones was achieved by reaction with Pd(OAc)2 and DABCO in DMF. The corresponding N-protected indolones undergo alkylation at C3.

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15

Gilman, Henry, and George F. Wright. "The diazotization of an aminofuran." Recueil des Travaux Chimiques des Pays-Bas 53, no. 1 (2010): 13–17. http://dx.doi.org/10.1002/recl.19340530104.

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16

LARGERON, M., and M. B. FLEURY. "ChemInform Abstract: Electrochemical Synthesis of 2-Substituted 5-Aminofurans." ChemInform 22, no. 50 (2010): no. http://dx.doi.org/10.1002/chin.199150051.

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17

Huynh, Thi Ngoc Tram, Pascal Retailleau, Clement Denhez, Kim Phi Phung Nguyen, and Dom Guillaume. "ChemInform Abstract: Regioselective Synthesis of 3,4,5-Trisubstituted 2-Aminofurans." ChemInform 45, no. 51 (2014): no. http://dx.doi.org/10.1002/chin.201451119.

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18

Alizadeh, Abdolali, Sadegh Rostamnia, Nasrin Zoreh, and Qasem Oskueyan. "A Novel Synthesis of Aminofurans Using a Four-Component Reaction." Synlett 2007, no. 10 (2007): 1610–12. http://dx.doi.org/10.1055/s-2007-982540.

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19

Ivanov, D. V., and N. M. Igidov. "INTERACTION OF SUBSTITUTED 2-AMINOFURANES WITH NUCLEOPHILIC AND ELECTROPHILIC REAGENTS (Review)." Вестник Пермского университета. Серия «Химия» = Bulletin of Perm University. CHEMISTRY 9, no. 2 (2019): 126–35. http://dx.doi.org/10.17072/2223-1838-2019-2-126-135.

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20

Chen, Yongtao, Shuaifeng Wang, Qianwen Jiang, Cungui Cheng, Xiaohui Xiao, and Gangguo Zhu. "Palladium-Catalyzed Site-Selective sp3 C–H Bond Thiocyanation of 2-Aminofurans." Journal of Organic Chemistry 83, no. 2 (2017): 716–22. http://dx.doi.org/10.1021/acs.joc.7b02700.

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21

Semmelhack, M. F., and Jaiwook Park. "Reaction of (aminocarbene)iron complexes with alkynes. A synthesis of 5-aminofurans." Organometallics 5, no. 12 (1986): 2550–52. http://dx.doi.org/10.1021/om00143a025.

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22

Redman, Anikó M., Jacques Dumas, and William J. Scott. "Preparation of 5-Substituted 3-Aminofuran-2-carboxylate Esters." Organic Letters 2, no. 14 (2000): 2061–63. http://dx.doi.org/10.1021/ol0059652.

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23

Mai, Shaoyu, and Qiuling Song. "Divergent Synthesis of Disulfanes and Benzenesulfonothioates Bearing 2-Aminofurans From N-Tosylhydrazone-Bearing Thiocarbamates." Angewandte Chemie International Edition 56, no. 27 (2017): 7952–57. http://dx.doi.org/10.1002/anie.201704091.

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24

Mai, Shaoyu, and Qiuling Song. "Divergent Synthesis of Disulfanes and Benzenesulfonothioates Bearing 2-Aminofurans From N-Tosylhydrazone-Bearing Thiocarbamates." Angewandte Chemie 129, no. 27 (2017): 8060–65. http://dx.doi.org/10.1002/ange.201704091.

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25

Wang, Le-Cheng, Hui-Qing Geng, Jin-Bao Peng, and Xiao-Feng Wu. "Iron-Catalyzed Synthesis of 2-Aminofurans from 2-Haloketones and Tertiary Amines or Enamines." European Journal of Organic Chemistry 2020, no. 17 (2020): 2605–16. http://dx.doi.org/10.1002/ejoc.202000293.

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26

Ma, Cheng, Hanfeng Ding, Guangming Wu, and Yewei Yang. "Facile Synthesis of Highly Substituted 3-Aminofurans from Thiazolium Salts, Aldehydes, and Dimethyl Acetylenedicarboxylate." Journal of Organic Chemistry 70, no. 22 (2005): 8919–23. http://dx.doi.org/10.1021/jo051513x.

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27

Jiang, Yaojia, Vanessa Zhong Yue Khong, Emmanuvel Lourdusamy, and Cheol-Min Park. "Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition." Chemical Communications 48, no. 25 (2012): 3133. http://dx.doi.org/10.1039/c2cc18139h.

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28

Ma, Cheng, and Yewei Yang. "Thiazolium-Mediated Multicomponent Reactions: A Facile Synthesis of 3-Aminofuran Derivatives." Organic Letters 7, no. 7 (2005): 1343–45. http://dx.doi.org/10.1021/ol0501368.

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29

Redman, Aniko M., Jacques Dumas, and William J. Scott. "ChemInform Abstract: Preparation of 5-Substituted 3-Aminofuran-2-carboxylate Esters." ChemInform 31, no. 43 (2000): no. http://dx.doi.org/10.1002/chin.200043124.

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30

Shen, Wen-Bo, Xiang-Ting Tang, Ting-Ting Zhang, Si-Yu Liu, Jiang-Man He, and Tong-Fu Su. "Cu(I)-Catalyzed Oxidative Cyclization of Enynamides: Regioselective Access to Cyclopentadiene Frameworks and 2-Aminofurans." Organic Letters 22, no. 17 (2020): 6799–804. http://dx.doi.org/10.1021/acs.orglett.0c02317.

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31

Akkurt, Mehmet, Senem Akkoç, Yetkin Gök, and Muhammad Nawaz Tahir. "1,3-Bis[(5-aminofuran-2-yl)methyl]-3,4,5,6-tetrahydropyrimidin-1-ium hexafluorophosphate." Acta Crystallographica Section E Structure Reports Online 69, no. 8 (2013): o1325. http://dx.doi.org/10.1107/s1600536813020187.

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32

Cheng, Cungui, Shuiyou Liu, and Gangguo Zhu. "Divergent Synthesis of 2-Aminofurans via Palladium-Catalyzed Acetoxylative, Alkoxylative, and Hydroxylative Cycloisomerization of Homoallenyl Amides." Journal of Organic Chemistry 80, no. 15 (2015): 7604–12. http://dx.doi.org/10.1021/acs.joc.5b01182.

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33

Borger, Maribel, and James H. Frederich. "Pyridazine N-Oxides as Precursors to 2-Aminofurans: Scope and Limitations in Complexity Building Cascade Reactions." Organic Letters 21, no. 7 (2019): 2397–401. http://dx.doi.org/10.1021/acs.orglett.9b00682.

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34

Jiang, Yaojia, Vanessa Zhong Yue Khong, Emmanuvel Lourdusamy, and Cheol-Min Park. "ChemInform Abstract: Synthesis of 2-Aminofurans and 2-Unsubstituted Furans via Carbenoid-Mediated [3 + 2] Cycloaddition." ChemInform 43, no. 30 (2012): no. http://dx.doi.org/10.1002/chin.201230118.

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35

Matiadis, Dimitris, Kyriakos Prousis, and Olga Igglessi-Markopoulou. "Solid-Phase Synthesis of Optically Active Substituted 2 Aminofuranones Using an Activated Carbonate Linker." Molecules 14, no. 10 (2009): 3914–21. http://dx.doi.org/10.3390/molecules14103914.

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36

Liang, Yong-Xin, Ming Yang, Bo-Wen He, and Yu-Long Zhao. "Silver-Catalyzed Cascade Cyclization Reaction of Isocyanides with Sulfoxonium Ylides: Synthesis of 3-Aminofurans and 4-Aminoquinolines." Organic Letters 22, no. 19 (2020): 7640–44. http://dx.doi.org/10.1021/acs.orglett.0c02835.

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37

Ye, Weijian, Chen Tan, Juan Yao, Shuwen Xue, Yang Li, and Cunde Wang. "Iodine-Promoted Domino Reactions of 1-Cyanocyclopropane 1-Esters: A Straightforward Approach to Fully Substituted 2-Aminofurans." Advanced Synthesis & Catalysis 358, no. 3 (2016): 426–34. http://dx.doi.org/10.1002/adsc.201500078.

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38

Dateer, Ramesh B., Kamalkishore Pati, and Rai-Shung Liu. "Gold-catalyzed synthesis of substituted 2-aminofurans via formal [4+1]-cycloadditions on 3-en-1-ynamides." Chemical Communications 48, no. 57 (2012): 7200. http://dx.doi.org/10.1039/c2cc33030j.

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39

Neo, Ana G., Ana Bornadiego, Jesús Díaz, Stefano Marcaccini, and Carlos F. Marcos. "Elusive 2-aminofuran Diels–Alder substrates for a straightforward synthesis of polysubstituted anilines." Organic & Biomolecular Chemistry 11, no. 38 (2013): 6546. http://dx.doi.org/10.1039/c3ob41411f.

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40

Nair, Vijay, A. Unni Vinod, N. Abhilash, et al. "Multicomponent reactions involving zwitterionic intermediates for the construction of heterocyclic systems: one pot synthesis of aminofurans and iminolactones." Tetrahedron 59, no. 51 (2003): 10279–86. http://dx.doi.org/10.1016/j.tet.2003.10.052.

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41

Yavari, Issa, Abdolali Alizadeh, Mohammad Anary-Abbasinejad, and Hamid R. Bijanzadeh. "Reaction between alkyl isocyanides and dibenzoylacetylene in the presence of strong NH-acids: synthesis of highly functionalized aminofurans." Tetrahedron 59, no. 32 (2003): 6083–86. http://dx.doi.org/10.1016/s0040-4020(03)00990-6.

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42

Cheng, Cungui, Shuiyou Liu, and Gangguo Zhu. "Palladium-Catalyzed Cycloisomerization and Aerobic Oxidative Cycloisomerization of Homoallenyl Amides: A Facile and Divergent Approach to 2-Aminofurans." Organic Letters 17, no. 6 (2015): 1581–84. http://dx.doi.org/10.1021/acs.orglett.5b00464.

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43

Cheng, Cungui, Shuiyou Liu, and Gangguo Zhu. "ChemInform Abstract: Divergent Synthesis of 2-Aminofurans via Palladium-Catalyzed Acetoxylative, Alkoxylative, and Hydroxylative Cycloisomerization of Homoallenyl Amides." ChemInform 46, no. 49 (2015): no. http://dx.doi.org/10.1002/chin.201549097.

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44

Hsu, Wei-Shun, Min-Huan Tsai, Indrajeet J. Barve, Gorakh S. Yellol, and Chung-Ming Sun. "Synthesis of Aminofuran-Linked Benzimidazoles and Cyanopyrrole-Fused Benzimidazoles by Condition-Based Skeletal Divergence." ACS Combinatorial Science 19, no. 7 (2017): 492–99. http://dx.doi.org/10.1021/acscombsci.7b00052.

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45

Yadav, J. S., B. V. Reddy, S. Shubashree, K. Sadashiv, and Jaisree J. Naidu. "Ionic Liquids-Promoted Multi-Component Reaction: Green Approach for Highly Substituted 2-Aminofuran Derivatives." Synthesis 2004, no. 14 (2004): 2376–80. http://dx.doi.org/10.1055/s-2004-831181.

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46

Dateer, Ramesh B., Kamalkishore Pati, and Rai-Shung Liu. "ChemInform Abstract: Gold-Catalyzed Synthesis of Substituted 2-Aminofurans via Formal [4 + 1]-Cycloadditions on 3-En-1-ynamides." ChemInform 43, no. 45 (2012): no. http://dx.doi.org/10.1002/chin.201245120.

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47

Li, Xingguang, Xu Ma, Zhixun Wang, Pei‐Nian Liu, and Liming Zhang. "Bifunctional Phosphine Ligand Enabled Gold‐Catalyzed Alkynamide Cycloisomerization: Access to Electron‐Rich 2‐Aminofurans and Their Diels–Alder Adducts." Angewandte Chemie International Edition 58, no. 48 (2019): 17180–84. http://dx.doi.org/10.1002/anie.201908598.

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48

Li, Xingguang, Xu Ma, Zhixun Wang, Pei‐Nian Liu, and Liming Zhang. "Bifunctional Phosphine Ligand Enabled Gold‐Catalyzed Alkynamide Cycloisomerization: Access to Electron‐Rich 2‐Aminofurans and Their Diels–Alder Adducts." Angewandte Chemie 131, no. 48 (2019): 17340–44. http://dx.doi.org/10.1002/ange.201908598.

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49

Neo, Ana G., Ana Bornadiego, Jesus Diaz, Stefano Marcaccini, and Carlos F. Marcos. "ChemInform Abstract: Elusive 2-Aminofuran Diels-Alder Substrates for a Straightforward Synthesis of Polysubstituted Anilines." ChemInform 45, no. 4 (2014): no. http://dx.doi.org/10.1002/chin.201404037.

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50

Cheng, Cungui, Shuiyou Liu, and Gangguo Zhu. "ChemInform Abstract: Palladium-Catalyzed Cycloisomerization and Aerobic Oxidative Cycloisomerization of Homoallenyl Amides: A Facile and Divergent Approach to 2-Aminofurans." ChemInform 46, no. 32 (2015): no. http://dx.doi.org/10.1002/chin.201532107.

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