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Journal articles on the topic 'Photoorganocatalysi'

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Author: Grafiati
Published: 1 April 2023

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1

Schiza, Andriana, Nikoleta Spiliopoulou, Adelajda Shahu, and Christoforos G. Kokotos. "Combining organocatalysis with photoorganocatalysis: photocatalytic hydroacylation of asymmetric organocatalytic Michael addition products." New Journal of Chemistry 42, no. 23 (2018): 18844–49. http://dx.doi.org/10.1039/c8nj04274h.

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2

Ravelli, Davide, Maurizio Fagnoni, and Angelo Albini. "Photoorganocatalysis. What for?" Chem. Soc. Rev. 42, no. 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, and Christoforos G. Kokotos. "Photoorganocatalytic synthesis of lactones via a selective C–H activation–alkylation of alcohols." Green Chemistry 19, no. 18 (2017): 4451–56. http://dx.doi.org/10.1039/c7gc01903c.

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4

Jia, Jiaqi, Quentin Lefebvre, and Magnus Rueping. "Reductive coupling of imines with redox-active esters by visible light photoredox organocatalysis." Organic Chemistry Frontiers 7, no. 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, and Angelo Albini. "ChemInform Abstract: Photoorganocatalysis. What for?" ChemInform 44, no. 18 (April 11, 2013): no. http://dx.doi.org/10.1002/chin.201318242.

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6

Ciszewski, Łukasz W., Sabina Smoleń, and Dorota Gryko. "Photoorganocatalytic α-oxyamination of aldehydes." Arkivoc 2017, no. 2 (September 20, 2016): 251–59. http://dx.doi.org/10.3998/ark.5550190.p009.769.

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7

Ravelli, Davide, and Maurizio Fagnoni. "Aromatic Aldehydes as Energy-Transfer Photoorganocatalysts." ChemCatChem 7, no. 5 (February 6, 2015): 735–37. http://dx.doi.org/10.1002/cctc.201403024.

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8

Kokotos, Christoforos, Ioanna Sideri, and Errika Voutyritsa. "Green Photoorganocatalytic Synthesis of Phenols from Arylboronic Acids." Synlett 29, no. 10 (November 24, 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, and Maurizio Fagnoni. "ChemInform Abstract: Aromatic Aldehydes as Energy-Transfer Photoorganocatalysts." ChemInform 46, no. 19 (April 23, 2015): no. http://dx.doi.org/10.1002/chin.201519312.

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10

Barata-Vallejo, Sebastián, Damian E. Yerien, Beatriz Lantano, and Al Postigo. "Transition Metal-free Photoorganocatalytic Fluoroalkylation Reactions of Organic Compounds." Current Organic Chemistry 20, no. 27 (October 28, 2016): 2838–47. http://dx.doi.org/10.2174/1385272820666160614080432.

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11

Papadopoulos, Giorgos N., and Christoforos G. Kokotos. "Photoorganocatalytic One-Pot Synthesis of Hydroxamic Acids from Aldehydes." Chemistry - A European Journal 22, no. 20 (April 1, 2016): 6964–67. http://dx.doi.org/10.1002/chem.201600333.

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12

Kokotos, Christoforos, Errika Voutyritsa, Nikolaos Nikitas, Mary Apostolopoulou, and Anna Gerogiannopoulou. "Photoorganocatalytic Atom Transfer Radical Addition of Bromoacetonitrile to Aliphatic Olefins." Synthesis 50, no. 17 (May 29, 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, and Christoforos G. Kokotos. "Photoorganocatalytic Hydroacylation of Dialkyl Azodicarboxylates by Utilising Activated Ketones as Photocatalysts." Chemistry – A European Journal 20, no. 42 (September 3, 2014): 13811–14. http://dx.doi.org/10.1002/chem.201403275.

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14

Papadopoulos, Giorgos N., Dimitris Limnios, and Christoforos G. Kokotos. "ChemInform Abstract: Photoorganocatalytic Hydroacylation of Dialkyl Azodicarboxylates by Utilising Activated Ketones as Photocatalysts." ChemInform 46, no. 13 (March 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, and Pierre Audebert. "s-Tetrazine: Robust and Green Photoorganocatalyst for Aerobic Oxidation of N,N-Disubstituted Hydroxylamines to Nitrones." Synlett 33, no. 02 (November 9, 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., and Christoforos G. Kokotos. "One-Pot Amide Bond Formation from Aldehydes and Amines via a Photoorganocatalytic Activation of Aldehydes." Journal of Organic Chemistry 81, no. 16 (June 3, 2016): 7023–28. http://dx.doi.org/10.1021/acs.joc.6b00488.

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17

Sideri, Ioanna K., Errika Voutyritsa, and 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, no. 25 (2018): 4596–614. http://dx.doi.org/10.1039/c8ob00725j.

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18

Huang, Ling, Jianzhang Zhao, Song Guo, Caishun Zhang, and Jie Ma. "Bodipy Derivatives as Organic Triplet Photosensitizers for Aerobic Photoorganocatalytic Oxidative Coupling of Amines and Photooxidation of Dihydroxylnaphthalenes." Journal of Organic Chemistry 78, no. 11 (May 23, 2013): 5627–37. http://dx.doi.org/10.1021/jo400769u.

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19

Lefebvre, Quentin, Norbert Hoffmann, and Magnus Rueping. "Photoorganocatalysed and visible light photoredox catalysed trifluoromethylation of olefins and (hetero)aromatics in batch and continuous flow." Chemical Communications 52, no. 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, and Malte Brasholz. "Photoorganocatalytic Aerobic Oxidative Amine Dehydrogenation/Super Acid‐Mediated Pictet‐Spengler Cyclization: Synthesis of cis ‐1,3‐Diaryl Tetrahydroisoquinolines." Advanced Synthesis & Catalysis 361, no. 12 (April 23, 2019): 2870–76. http://dx.doi.org/10.1002/adsc.201900165.

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21

"Biomimetic Photoorganocatalytic Chlorination of Arenes." Synfacts 12, no. 06 (May 17, 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, no. 11 (October 18, 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, no. 02 (January 18, 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, no. 08 (July 18, 2017): 0869. http://dx.doi.org/10.1055/s-0036-1590697.

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25

Abbasova, Gulu, and Ajdar Medjidov. "One-pot synthesis of the new Hydroxamic acid and its complexes with metals." Letters in Organic Chemistry 19 (January 11, 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., and Christoforos G. Kokotos. "ChemInform Abstract: Photoorganocatalytic One-Pot Synthesis of Hydroxamic Acids from Aldehydes." ChemInform 47, no. 39 (September 2016). http://dx.doi.org/10.1002/chin.201639063.

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