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Photoredox-Enabled Decarboxylative Synthesis of Unnatural α-Amino Acids
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemistry, Organic chemistry.ORCID iD: 0000-0002-7249-7437
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemistry, Organic chemistry.ORCID iD: 0000-0002-6089-5454
2022 (English)In: Synlett: Accounts and Rapid Communications in Synthetic Organic Chemistry, ISSN 0936-5214, E-ISSN 1437-2096, Vol. 33, no 2, p. 109-115Article in journal (Refereed) Published
Abstract [en]

Recently, development of general synthetic routes to unnatural α-amino acids has gained significant momentum, driven by the high demand for such building blocks in fundamental research within molecular and structural biology, as well as for development of new pharmaceuticals. Herein, we highlight the recent progress in employing photoredox-mediated synthetic methods for accessing unnatural α-amino acids with a focus on various decarboxylative radical-based strategies. 

Place, publisher, year, edition, pages
Georg Thieme Verlag KG , 2022. Vol. 33, no 2, p. 109-115
Keywords [en]
amino acids, decarboxylation, photoredox catalysis, radicals
National Category
Organic Chemistry
Identifiers
URN: urn:nbn:se:kth:diva-310139DOI: 10.1055/a-1499-8679ISI: 000664712000001Scopus ID: 2-s2.0-85108881946OAI: oai:DiVA.org:kth-310139DiVA, id: diva2:1647705
Note

QC 20220328

Available from: 2022-03-28 Created: 2022-03-28 Last updated: 2022-06-25Bibliographically approved

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Shatskiy, AndreyKärkäs, Markus D.

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