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Artigos de revistas sobre o tema "Ene-ynamides"

Autor: Grafiati
Publicado: 23 de novembro de 2024

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Veja os 21 melhores artigos de revistas para estudos sobre o assunto "Ene-ynamides".

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1

Wakamatsu, Hideaki, Yuichi Yoshimura, Yoshimi Sasaki, Masatoshi Kawahata e Kentaro Yamaguchi. "Synthesis of Various Heterocycles Having a Dienamide Moiety by Ring-Closing Metathesis of Ene-ynamides". Synthesis 50, n.º 17 (30 de maio de 2018): 3467–86. http://dx.doi.org/10.1055/s-0037-1609857.

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Ring-closing metathesis (RCM) of ynamides, having alkene substituents of various lengths on the side chain, was demonstrated using the second-generation Grubbs catalyst. When the reaction of ene-ynamides was carried out in the presence of 5 mol% of the catalyst, RCM proceeded smoothly to give quinoline or isoquinoline derivatives having a dienamide unit in good yields. Furthermore, RCM of ene-ynamides, having one more carbon on the side chain, proceeded smoothly to provide seven-membered heterocycles having a dienamide component. Similarly, eight-membered heterocycles, diazocine and benzodiazocine, were also synthesized by RCM of ene-ynamides in good yields.
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2

Couty, Sylvain, Christophe Meyer e Janine Cossy. "Gold-catalyzed cycloisomerizations of ene-ynamides". Tetrahedron 65, n.º 9 (fevereiro de 2009): 1809–32. http://dx.doi.org/10.1016/j.tet.2008.10.108.

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3

Deng, Yongming, Jason Zhang, Bradley Bankhead, Jonathan P. Markham e Matthias Zeller. "Photoinduced oxidative cyclopropanation of ene-ynamides: synthesis of 3-aza[n.1.0]bicycles via vinyl radicals". Chemical Communications 57, n.º 43 (2021): 5254–57. http://dx.doi.org/10.1039/d1cc02016a.

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4

Marion, Frédéric, Julien Coulomb, Christine Courillon, Louis Fensterbank e Max Malacria. "Platinum Dichloride-Catalyzed Cycloisomerization of Ene-ynamides". Organic Letters 6, n.º 9 (abril de 2004): 1509–11. http://dx.doi.org/10.1021/ol049530g.

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5

Cossy, J., S. Couty e C. Meyer. "Cycloisomerizations of Ene-Ynamides Mediated by Gold". Synfacts 2006, n.º 12 (dezembro de 2006): 1241. http://dx.doi.org/10.1055/s-2006-955636.

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6

Couty, Sylvain, Christophe Meyer e Janine Cossy. "Diastereoselective Gold-Catalyzed Cycloisomerizations of Ene-Ynamides". Angewandte Chemie 118, n.º 40 (13 de outubro de 2006): 6878–82. http://dx.doi.org/10.1002/ange.200602270.

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7

Couty, Sylvain, Christophe Meyer e Janine Cossy. "Diastereoselective Gold-Catalyzed Cycloisomerizations of Ene-Ynamides". Angewandte Chemie International Edition 45, n.º 40 (13 de outubro de 2006): 6726–30. http://dx.doi.org/10.1002/anie.200602270.

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8

Nishimura, Takahiro, Yuka Takiguchi, Yuko Maeda e Tamio Hayashi. "Rhodium-Catalyzed Asymmetric Cycloisomerization of 1,6-Ene-ynamides". Advanced Synthesis & Catalysis 355, n.º 7 (30 de abril de 2013): 1374–82. http://dx.doi.org/10.1002/adsc.201300148.

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9

Nishimura, Takahiro, Yuka Takiguchi, Yuko Maeda e Tamio Hayashi. "ChemInform Abstract: Rhodium-Catalyzed Asymmetric Cycloisomerization of 1,6-Ene-ynamides." ChemInform 44, n.º 38 (30 de agosto de 2013): no. http://dx.doi.org/10.1002/chin.201338161.

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10

Huang, Jian, Hui Xiong, Richard P. Hsung, C. Rameshkumar, Jason A. Mulder e Tyler P. Grebe. "The First Successful Base-Promoted Isomerization of Propargyl Amides to Chiral Ynamides. Applications in Ring-Closing Metathesis of Ene−Ynamides and Tandem RCM of Diene−Ynamides". Organic Letters 4, n.º 14 (julho de 2002): 2417–20. http://dx.doi.org/10.1021/ol020097p.

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11

Huang, Jian, Hui Xiong, Richard P. Hsung, C. Rameshkumar, Jason A. Mulder e Tyler P. Grebe. "ChemInform Abstract: The First Successful Base-Promoted Isomerization of Propargyl Amides to Chiral Ynamides. Applications in Ring-Closing Metathesis of Ene-Ynamides and Tandem RCM of Diene-Ynamides." ChemInform 33, n.º 49 (18 de maio de 2010): no. http://dx.doi.org/10.1002/chin.200249073.

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12

Meyer, Christophe, Sylvain Couty e Janine Cossy. "Chemoselective Epoxidation of Ene-Ynamides: Intramolecular Cyclopropanation Induced by the Intermediate α-Oxocarbene". Synlett 2007, n.º 18 (12 de outubro de 2007): 2819–22. http://dx.doi.org/10.1055/s-2007-990841.

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13

Li, Sifan, Yu Wang, Zibo Wu, Weiliang Shi, Yibo Lei, Paul W. Davies e Wei Shu. "A Radical-Initiated Fragmentary Rearrangement Cascade of Ene-Ynamides to [1,2]-Annulated Indoles via Site-Selective Cyclization". Organic Letters 23, n.º 18 (28 de agosto de 2021): 7209–14. http://dx.doi.org/10.1021/acs.orglett.1c02519.

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14

Marion, Frederic, Julien Coulomb, Christine Courillon, Louis Fensterbank e Max Malacria. "Platinum Dichloride Catalyzed Cycloisomerization of Ene-ynamides." ChemInform 35, n.º 36 (7 de setembro de 2004). http://dx.doi.org/10.1002/chin.200436031.

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15

Couty, Sylvain, Christophe Meyer e Janine Cossy. "Diastereoselective Gold-Catalyzed Cycloisomerizations of Ene-Ynamides." ChemInform 38, n.º 6 (6 de fevereiro de 2007). http://dx.doi.org/10.1002/chin.200706038.

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16

Couty, Sylvain, Christophe Meyer e Janine Cossy. "ChemInform Abstract: Gold-Catalyzed Cycloisomerizations of Ene-ynamides." ChemInform 40, n.º 27 (7 de julho de 2009). http://dx.doi.org/10.1002/chin.200927026.

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17

Yamaoka, Yousuke, Nao Takeuchi, Ken‐ichi Yamada e Kiyosei Takasu. "Efficient Synthesis of Medium‐sized Nitrogen Heterocycles by Brønsted Acid‐Catalyzed Cyclization of Ene‐ynamides". Asian Journal of Organic Chemistry, 27 de abril de 2023. http://dx.doi.org/10.1002/ajoc.202300145.

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18

Hourtoule, Maxime, e Laurence Miesch. "Regio- and Stereoselective Addition to gem-Difluorinated Ene–Ynamides: Access to Stereodefined Fluorinated Dienes". Organic Letters, 19 de maio de 2022. http://dx.doi.org/10.1021/acs.orglett.2c01593.

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19

Zhu, Bo-Han, Cang-Hai Shen, Min-Ling Nie, Fumin Zheng, Chengzhe Huang, Fan Chen, Long Li, Chao Deng, Long-Wu Ye e Peng-Cheng Qian. "Highly Site-Selective Oxidative Cyclization of Ene-ynamides via Non-Noble-Metal Catalysis: Access to Functionalized Lactams". Organic Letters, 19 de setembro de 2022. http://dx.doi.org/10.1021/acs.orglett.2c02871.

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20

Wang, Nan, Hao-Jin Xu, Ting Li, Long-Wu Ye e Bo Zhou. "Copper-Catalyzed [2 + 2] Cyclization/Ring Expansion of Ene-Ynamides: Construction of Medium- and Large-Sized Rings". Organic Letters, 28 de abril de 2024. http://dx.doi.org/10.1021/acs.orglett.4c01013.

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21

Sahoo, Akhila Kumar, Prasad Rangu, Kanikarapu Suresh, Shubham Dutta e Srinivas Vangara. "Metal-Free Stereoselective Addition of Propiolic acids to Ynamides: A Concise Synthetic Route to Highly Substituted Ene-Diyne/Dienyne-(E)-N,O-Acetals". New Journal of Chemistry, 2022. http://dx.doi.org/10.1039/d2nj01907h.

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A straight forward and sustainable approach for 1,2-addition of propiolic acids to ynamide has led to bench stable sp2 (E)-enol-enamides of enediynes & dienynes. The reaction is chemo, regio, as...
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