A Copper‐Catalyzed Interrupted Domino Reaction for the Synthesis of Fused Triazolyl Benzothiadiazine‐1‐oxides
| dc.contributor.author | Hommelsheim, Renè | |
| dc.contributor.author | Bausch, Sandra | |
| dc.contributor.author | Selvakumar, Arjuna | |
| dc.contributor.author | Amer, Mostafa M. | |
| dc.contributor.author | Truong, Khai-Nghi | |
| dc.contributor.author | Rissanen, Kari | |
| dc.contributor.author | Bolm, Carsten | |
| dc.date.accessioned | 2023-03-14T07:18:38Z | |
| dc.date.available | 2023-03-14T07:18:38Z | |
| dc.date.issued | 2023 | |
| dc.identifier.citation | Hommelsheim, R., Bausch, S., Selvakumar, A., Amer, M. M., Truong, K.-N., Rissanen, K., & Bolm, C. (2023). A Copper‐Catalyzed Interrupted Domino Reaction for the Synthesis of Fused Triazolyl Benzothiadiazine‐1‐oxides. <i>Chemistry: A European Journal</i>, <i>29</i>(13), Article e202203729. <a href="https://doi.org/10.1002/chem.202203729" target="_blank">https://doi.org/10.1002/chem.202203729</a> | |
| dc.identifier.other | CONVID_164441954 | |
| dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/85999 | |
| dc.description.abstract | Copper(I)-catalyzed domino reactions of 2-azido sulfoximines with 1-iodoalkynes yield fused triazolyl-containing benzothiadiazine-1-oxides. The protocol features the synthesis of two fused heterocyclic rings in one step with good to excellent yields and a broad functional group tolerance. Detailed mechanistic investigations indicate that a copper π-complex initiates a cycloaddition and oxidative C–N coupling reaction sequence. The results suggest an interrupted domino process involving an iodinated triazole as a key intermediate. | en |
| dc.format.mimetype | application/pdf | |
| dc.language.iso | eng | |
| dc.publisher | Wiley-VCH Verlag | |
| dc.relation.ispartofseries | Chemistry: A European Journal | |
| dc.rights | CC BY 4.0 | |
| dc.title | A Copper‐Catalyzed Interrupted Domino Reaction for the Synthesis of Fused Triazolyl Benzothiadiazine‐1‐oxides | |
| dc.type | research article | |
| dc.identifier.urn | URN:NBN:fi:jyu-202303142153 | |
| dc.contributor.laitos | Kemian laitos | fi |
| dc.contributor.laitos | Department of Chemistry | en |
| dc.contributor.oppiaine | Orgaaninen kemia | fi |
| dc.contributor.oppiaine | Organic Chemistry | en |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
| dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
| dc.description.reviewstatus | peerReviewed | |
| dc.relation.issn | 0947-6539 | |
| dc.relation.numberinseries | 13 | |
| dc.relation.volume | 29 | |
| dc.type.version | publishedVersion | |
| dc.rights.copyright | © 2022 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH | |
| dc.rights.accesslevel | openAccess | fi |
| dc.type.publication | article | |
| dc.subject.yso | katalyysi | |
| dc.subject.yso | kemiallinen synteesi | |
| dc.subject.yso | heterosykliset yhdisteet | |
| dc.subject.yso | kupari | |
| dc.format.content | fulltext | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p8704 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p8468 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p38837 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p19074 | |
| dc.rights.url | https://creativecommons.org/licenses/by/4.0/ | |
| dc.relation.doi | 10.1002/chem.202203729 | |
| jyx.fundinginformation | R.H. gratefully acknowledges support by the Fonds der Chemischen Industrie e.V. (Kekulé scholarship) and by the Friedrich-Ebert-Stiftung (Promotionsförderung). M. M. Amer thanks the Leibniz-Gemeinschaft for financial support (project PHARMSA K136/2018), and we acknowledge the Alexander von Humboldt Foundation for support of K.R. (AvH research award). The authors thank Mrs. Susanne Pohlmann for her support in synthetic work, Christian Schumacher for his help in the preparation of X-ray samples and fruitful discussion, Victoria Pfennig for critical proofreading, and Dr. Christoph Räuber (all RWTH Aachen University) for mechanistic NMR studies. | |
| dc.type.okm | A1 |
Files in this item
This item appears in the following Collection(s)
Except where otherwise noted, this item's license is described as CC BY 4.0