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Accelerating stereoselective radical cross-couplings
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemistry, Organic chemistry.ORCID iD: 0009-0006-2467-5338
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemistry.ORCID iD: 0000-0002-8296-7455
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemistry, Organic chemistry.ORCID iD: 0000-0002-6089-5454
2025 (English)In: Nature Chemistry, ISSN 1755-4330, E-ISSN 1755-4349, Vol. 17, no 1, p. 8-10Article in journal (Refereed) Published
Abstract [en]

Aminoalcohols are vital motifs in chemical synthesis; however, traditional synthetic technologies relying on polar disconnections have various limitations. Now, such motifs can be expediently accessed by leveraging a radical-based approach, enabling the stereoselective preparation of an array of valuable building blocks.

Place, publisher, year, edition, pages
Springer Nature , 2025. Vol. 17, no 1, p. 8-10
National Category
Basic Medicine
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URN: urn:nbn:se:kth:diva-358776DOI: 10.1038/s41557-024-01702-xISI: 001392976900006PubMedID: 39775218Scopus ID: 2-s2.0-85214574875OAI: oai:DiVA.org:kth-358776DiVA, id: diva2:1929781
Note

QC 20250121

Available from: 2025-01-21 Created: 2025-01-21 Last updated: 2025-01-21Bibliographically approved

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Alvey, Gregory R.Avetian, David L.Kärkäs, Markus D.

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