Relevant bibliographies by topics / Photoorganocatalysi

Academic literature on the topic 'Photoorganocatalysi'

Author: Grafiati
Published: 1 April 2023

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Contents

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Photoorganocatalysi.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Photoorganocatalysi"

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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.
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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.
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Books on the topic "Photoorganocatalysi"

1

Fagnoni, Maurizio, Stefano Protti, and Davide Ravelli. Photoorganocatalysis in Organic Synthesis. WORLD SCIENTIFIC (EUROPE), 2018. http://dx.doi.org/10.1142/q0180.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Fagnoni, Maurizio, Stefano Protti, and Davide Ravelli. Photoorganocatalysis in Organic Synthesis. World Scientific Publishing Co Pte Ltd, 2019.

Find full text
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Photoorganocatalysi"

1

Anselmo, Manuel, Andrea Basso, and Lisa Moni. "Photoorganocatalysis in Flow." In Photoorganocatalysis in Organic Synthesis, 519–58. WORLD SCIENTIFIC (EUROPE), 2019. http://dx.doi.org/10.1142/9781786346056_0012.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Gigmes, Didier, Frédéric Dumur, Nicolas Zivic, Ségolène Villotte, Jason C. Morris, Jacques Lalevée, and Aude Héloïse Bonardi. "Photoorganocatalysts for Polymerization." In Photoorganocatalysis in Organic Synthesis, 471–518. WORLD SCIENTIFIC (EUROPE), 2019. http://dx.doi.org/10.1142/9781786346056_0011.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Kamijo, Shin. "Ketones and Aldehydes." In Photoorganocatalysis in Organic Synthesis, 1–37. WORLD SCIENTIFIC (EUROPE), 2019. http://dx.doi.org/10.1142/9781786346056_0001.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Itoh, Akichika. "Quinones." In Photoorganocatalysis in Organic Synthesis, 39–70. WORLD SCIENTIFIC (EUROPE), 2019. http://dx.doi.org/10.1142/9781786346056_0002.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Protti, Stefano, and Davide Ravelli. "Aromatics and Cyanoaromatics." In Photoorganocatalysis in Organic Synthesis, 71–111. WORLD SCIENTIFIC (EUROPE), 2019. http://dx.doi.org/10.1142/9781786346056_0003.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Goliszewska, Katarzyna, Katarzyna Orłowska, and Dorota Gryko. "Sulfur Heterocycles." In Photoorganocatalysis in Organic Synthesis, 113–81. WORLD SCIENTIFIC (EUROPE), 2019. http://dx.doi.org/10.1142/9781786346056_0004.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Bonesi, Sergio M., and Al Postigo. "Oxygen Heterocycles: Pyrylium Salts." In Photoorganocatalysis in Organic Synthesis, 183–242. WORLD SCIENTIFIC (EUROPE), 2019. http://dx.doi.org/10.1142/9781786346056_0005.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Xiao, Wen-Jing, Xiao-Qiang Hu, and Jia-Rong Chen. "Oxygen Heterocycles: Eosin Derivatives." In Photoorganocatalysis in Organic Synthesis, 243–86. WORLD SCIENTIFIC (EUROPE), 2019. http://dx.doi.org/10.1142/9781786346056_0006.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Leonori, Daniele, and Fabio Juliá. "Oxygen Heterocycles: Fluorescein, Rhodamines, Rose Bengal." In Photoorganocatalysis in Organic Synthesis, 287–315. WORLD SCIENTIFIC (EUROPE), 2019. http://dx.doi.org/10.1142/9781786346056_0007.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

García, Hermenegildo, and Sonia Remiro-Buenamañana. "Nitrogen Heterocycles: Porphyrins." In Photoorganocatalysis in Organic Synthesis, 317–57. WORLD SCIENTIFIC (EUROPE), 2019. http://dx.doi.org/10.1142/9781786346056_0008.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Photoorganocatalysi' for particular source types:
Journal articles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography