• No results found

Correction to Pd-Catalyzed de Novo Assembly of Diversely Substituted Indole-Fused Polyheterocycles

N/A
N/A
Protected

Academic year: 2021

Share "Correction to Pd-Catalyzed de Novo Assembly of Diversely Substituted Indole-Fused Polyheterocycles"

Copied!
2
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

University of Groningen

Correction to Pd-Catalyzed de Novo Assembly of Diversely Substituted Indole-Fused

Polyheterocycles

Wang, Qian; Osipyan, Angelina; Konstantinidou, Markella; Butera, Roberto; Mgimpatsang,

Kumchok C; Shishkina, Svitlana V; Dömling, Alexander

Published in:

The Journal of Organic Chemistry

DOI:

10.1021/acs.joc.0c01202

IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from it. Please check the document version below.

Document Version

Publisher's PDF, also known as Version of record

Publication date: 2020

Link to publication in University of Groningen/UMCG research database

Citation for published version (APA):

Wang, Q., Osipyan, A., Konstantinidou, M., Butera, R., Mgimpatsang, K. C., Shishkina, S. V., & Dömling, A. (2020). Correction to Pd-Catalyzed de Novo Assembly of Diversely Substituted Indole-Fused

Polyheterocycles. The Journal of Organic Chemistry, 85(12), [8295]. https://doi.org/10.1021/acs.joc.0c01202

Copyright

Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons).

Take-down policy

If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim.

Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum.

(2)

Correction to Pd-Catalyzed de Novo Assembly of Diversely

Substituted Indole-Fused Polyheterocycles

Qian Wang, Angelina Osipyan, Markella Konstantinidou, Roberto Butera, Kumchok C. Mgimpatsang,

Svitlana V. Shishkina, and Alexander Dömling

*

J. Org. Chem. 2019, 84, (18), 12148−12156. DOI:10.1021/acs.joc.9b01258

Cite This:J. Org. Chem. 2020, 85, 8295−8295 Read Online

ACCESS

Metrics & More Article Recommendations

I

ncomplete grant information was provided in the original Acknowledgments.

ACKNOWLEDGMENTS

The project leading to this application has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie agreement No. 675555, No. 713482, and No. 754425. Q.W. acknowledges the China Scholarship Council for support.

Published: June 10, 2020

Addition/Correction pubs.acs.org/joc

© 2020 American Chemical Society 8295

https://dx.doi.org/10.1021/acs.joc.0c01202

J. Org. Chem. 2020, 85, 8295−8295

This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License, which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.

Downloaded via UNIV GRONINGEN on July 29, 2020 at 07:57:05 (UTC).

Referenties

GERELATEERDE DOCUMENTEN

Then, the solvent was removed under reduced pressure and the crude reaction mixture was purified by column chromatography (eluent: PE – EA [0 to 100% EtOAc in PE]).. For

With the optimized one-pot reaction conditions in hand, the scope of the “Ugi-4CR/cyclization” reaction was further investigated by reacting propargylamine with

A Ugi 4-component reaction with indole-2-carboxylic acid and an aniline followed by a Pd-catalyzed cyclization yields tetracyclic indoloquinolines in good to moderate

The reaction mixture was stirred at room temperature for 24 h to obtain intermediates A; then the solvent was removed and acetic anhydride [0.5 M] and 4N HCl in dioxane (1.0

After the completion of the reaction, the mixture was concentrated under reduced pressure and in the residue was added aryl chloride 6 (0.75 mmol), pyridine (1 ml) and the

The catalytic dyad (D35 and D 219) is represented by stick models. Oxygen atoms are colored in red and nitrogen atoms in blue. On the right, close-up view of the accommodation

Until recently, the design of PROTACs mostly considered the formation of the complex with the proteins as two binary interactions, in which the two warheads were optimized

were removed under reduced pressure and the crude was purified by column chromatography with DCM – MeOH – NH 3 (85 : 10: 5) to obtain the pure product. 13 C NMR has