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Artículos de revistas sobre el tema "Photoorganocatalysi"

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Autor: Grafiati
Publicado: 1 de abril de 2023

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1

Schiza, Andriana, Nikoleta Spiliopoulou, Adelajda Shahu y Christoforos G. Kokotos. "Combining organocatalysis with photoorganocatalysis: photocatalytic hydroacylation of asymmetric organocatalytic Michael addition products". New Journal of Chemistry 42, n.º 23 (2018): 18844–49. http://dx.doi.org/10.1039/c8nj04274h.

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2

Ravelli, Davide, Maurizio Fagnoni y Angelo Albini. "Photoorganocatalysis. What for?" Chem. Soc. Rev. 42, n.º 1 (2013): 97–113. http://dx.doi.org/10.1039/c2cs35250h.

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3

Kaplaneris, Nikolaos, Aikaterini Bisticha, Giorgos N. Papadopoulos, Dimitris Limnios y Christoforos G. Kokotos. "Photoorganocatalytic synthesis of lactones via a selective C–H activation–alkylation of alcohols". Green Chemistry 19, n.º 18 (2017): 4451–56. http://dx.doi.org/10.1039/c7gc01903c.

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4

Jia, Jiaqi, Quentin Lefebvre y Magnus Rueping. "Reductive coupling of imines with redox-active esters by visible light photoredox organocatalysis". Organic Chemistry Frontiers 7, n.º 3 (2020): 602–8. http://dx.doi.org/10.1039/c9qo01428d.

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The direct alkylation of imines with redox-active esters by visible light photoorganocatalysis provides a direct way for accessing α-branched secondary amines which are found in numerous bioactive molecules.
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5

Ravelli, Davide, Maurizio Fagnoni y Angelo Albini. "ChemInform Abstract: Photoorganocatalysis. What for?" ChemInform 44, n.º 18 (11 de abril de 2013): no. http://dx.doi.org/10.1002/chin.201318242.

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6

Ciszewski, Łukasz W., Sabina Smoleń y Dorota Gryko. "Photoorganocatalytic α-oxyamination of aldehydes". Arkivoc 2017, n.º 2 (20 de septiembre de 2016): 251–59. http://dx.doi.org/10.3998/ark.5550190.p009.769.

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7

Ravelli, Davide y Maurizio Fagnoni. "Aromatic Aldehydes as Energy-Transfer Photoorganocatalysts". ChemCatChem 7, n.º 5 (6 de febrero de 2015): 735–37. http://dx.doi.org/10.1002/cctc.201403024.

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8

Kokotos, Christoforos, Ioanna Sideri y Errika Voutyritsa. "Green Photoorganocatalytic Synthesis of Phenols from Arylboronic Acids". Synlett 29, n.º 10 (24 de noviembre de 2017): 1324–28. http://dx.doi.org/10.1055/s-0036-1591837.

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A green and cheap protocol for the photocatalytic hydroxylation of arylboronic acids is presented. 2,2-Dimethoxy-2-phenylacetophenone proved to be the best photoinitiator, among a range of organocatalysts in promoting this reaction. This photocatalytic protocol can be expanded into a wide substrate scope of aromatic boronic acids bearing various functional groups, leading to the corresponding phenols in good to high yields under mild reaction conditions, which include water as solvent, light irradiation provided from standard light-bulbs at room temperature.
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9

Ravelli, Davide y Maurizio Fagnoni. "ChemInform Abstract: Aromatic Aldehydes as Energy-Transfer Photoorganocatalysts". ChemInform 46, n.º 19 (23 de abril de 2015): no. http://dx.doi.org/10.1002/chin.201519312.

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10

Barata-Vallejo, Sebastián, Damian E. Yerien, Beatriz Lantano y Al Postigo. "Transition Metal-free Photoorganocatalytic Fluoroalkylation Reactions of Organic Compounds". Current Organic Chemistry 20, n.º 27 (28 de octubre de 2016): 2838–47. http://dx.doi.org/10.2174/1385272820666160614080432.

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11

Papadopoulos, Giorgos N. y Christoforos G. Kokotos. "Photoorganocatalytic One-Pot Synthesis of Hydroxamic Acids from Aldehydes". Chemistry - A European Journal 22, n.º 20 (1 de abril de 2016): 6964–67. http://dx.doi.org/10.1002/chem.201600333.

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12

Kokotos, Christoforos, Errika Voutyritsa, Nikolaos Nikitas, Mary Apostolopoulou y Anna Gerogiannopoulou. "Photoorganocatalytic Atom Transfer Radical Addition of Bromoacetonitrile to Aliphatic Olefins". Synthesis 50, n.º 17 (29 de mayo de 2018): 3395–401. http://dx.doi.org/10.1055/s-0037-1610138.

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A green and cheap protocol for the photocatalytic atom transfer radical addition (ATRA) of bromoacetonitrile to aliphatic alkenes is presented. The use of benzoin methyl ehter as the photocatalyst and irradiation using a household lightbulb leads to a highly useful synthetic method for the conversion of a wide range of substituted aliphatic olefins into the corresponding bromonitriles.
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13

Papadopoulos, Giorgos N., Dimitris Limnios y Christoforos G. Kokotos. "Photoorganocatalytic Hydroacylation of Dialkyl Azodicarboxylates by Utilising Activated Ketones as Photocatalysts". Chemistry – A European Journal 20, n.º 42 (3 de septiembre de 2014): 13811–14. http://dx.doi.org/10.1002/chem.201403275.

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14

Papadopoulos, Giorgos N., Dimitris Limnios y Christoforos G. Kokotos. "ChemInform Abstract: Photoorganocatalytic Hydroacylation of Dialkyl Azodicarboxylates by Utilising Activated Ketones as Photocatalysts." ChemInform 46, n.º 13 (marzo de 2015): no. http://dx.doi.org/10.1002/chin.201513075.

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15

Masson, Géraldine, Jiyuan Lyu, Tuan Le, Aurélie Claraz, Clémence Allain y Pierre Audebert. "s-Tetrazine: Robust and Green Photoorganocatalyst for Aerobic Oxidation of N,N-Disubstituted Hydroxylamines to Nitrones". Synlett 33, n.º 02 (9 de noviembre de 2021): 177–81. http://dx.doi.org/10.1055/a-1691-0449.

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AbstractEfficient photocatalytic aerobic oxidative dehydrogenation reactions of N,N-disubstituted hydroxylamines to nitrones were developed with an in situ generated photocatalyst based on commercially available 3,6-dichlorotetrazine. This process affords a wide range of nitrones in high yields under mild conditions. In addition, an oxidative (3+3) cycloaddition between an oxyallyl cation precursor and a hydroxylamine was also developed.
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16

Papadopoulos, Giorgos N. y Christoforos G. Kokotos. "One-Pot Amide Bond Formation from Aldehydes and Amines via a Photoorganocatalytic Activation of Aldehydes". Journal of Organic Chemistry 81, n.º 16 (3 de junio de 2016): 7023–28. http://dx.doi.org/10.1021/acs.joc.6b00488.

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17

Sideri, Ioanna K., Errika Voutyritsa y Christoforos G. Kokotos. "Photoorganocatalysis, small organic molecules and light in the service of organic synthesis: the awakening of a sleeping giant". Organic & Biomolecular Chemistry 16, n.º 25 (2018): 4596–614. http://dx.doi.org/10.1039/c8ob00725j.

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18

Huang, Ling, Jianzhang Zhao, Song Guo, Caishun Zhang y Jie Ma. "Bodipy Derivatives as Organic Triplet Photosensitizers for Aerobic Photoorganocatalytic Oxidative Coupling of Amines and Photooxidation of Dihydroxylnaphthalenes". Journal of Organic Chemistry 78, n.º 11 (23 de mayo de 2013): 5627–37. http://dx.doi.org/10.1021/jo400769u.

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19

Lefebvre, Quentin, Norbert Hoffmann y Magnus Rueping. "Photoorganocatalysed and visible light photoredox catalysed trifluoromethylation of olefins and (hetero)aromatics in batch and continuous flow". Chemical Communications 52, n.º 12 (2016): 2493–96. http://dx.doi.org/10.1039/c5cc09881e.

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Trifluoromethylation of olefins and (hetero)aromatics with sodium triflinate as CF3source and readily accessible benzophenone derivatives as photosensitisers has been developed in batch and flow.
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20

Unkel, Lisa‐Natascha, Simon Malcherek, Eva Schendera, Frank Hoffmann, Julia Rehbein y Malte Brasholz. "Photoorganocatalytic Aerobic Oxidative Amine Dehydrogenation/Super Acid‐Mediated Pictet‐Spengler Cyclization: Synthesis of cis ‐1,3‐Diaryl Tetrahydroisoquinolines". Advanced Synthesis & Catalysis 361, n.º 12 (23 de abril de 2019): 2870–76. http://dx.doi.org/10.1002/adsc.201900165.

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21

"Biomimetic Photoorganocatalytic Chlorination of Arenes". Synfacts 12, n.º 06 (17 de mayo de 2016): 0638. http://dx.doi.org/10.1055/s-0035-1562139.

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22

"Photoorganocatalytic Radical Reaction of Cinnamaldehydes and Olefins". Synfacts 14, n.º 11 (18 de octubre de 2018): 1191. http://dx.doi.org/10.1055/s-0037-1611046.

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23

"Enantioselective Photoorganocatalytic Synthesis of 1,4-Dicarbonyl Compounds". Synfacts 15, n.º 02 (18 de enero de 2019): 0199. http://dx.doi.org/10.1055/s-0037-1612031.

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24

"Enantioselective Photoorganocatalytic Formal α-Alkylation of Aldehydes". Synfacts 13, n.º 08 (18 de julio de 2017): 0869. http://dx.doi.org/10.1055/s-0036-1590697.

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25

Abbasova, Gulu y Ajdar Medjidov. "One-pot synthesis of the new Hydroxamic acid and its complexes with metals". Letters in Organic Chemistry 19 (11 de enero de 2022). http://dx.doi.org/10.2174/1570178619666220111121743.

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Abstract: A one-pot conversion of 2-hydroxy-1-naphthoic aldehyde to hydroxamic acid was described. An efficient photoorganocatalytic method of synthesis was developed. The obtained hydroxamic acid was identified by various physicochemical methods such as IR, UV- and NMR-spectroscopy. Solid colored complexes of copper (II) and iron (II), respectively, green and brown colours with the obtained hydroxamic acid were synthesized in ethanol medium for the first time. The molar ratio of ligand and metal in the complex was 2:1. Their structures were established using IR, UV- spectroscopy and thermogravimetric analysis.
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26

Papadopoulos, Giorgos N. y Christoforos G. Kokotos. "ChemInform Abstract: Photoorganocatalytic One-Pot Synthesis of Hydroxamic Acids from Aldehydes." ChemInform 47, n.º 39 (septiembre de 2016). http://dx.doi.org/10.1002/chin.201639063.

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