Näytä suppeat kuvailutiedot

dc.contributor.authorYedigenov, Mussa
dc.contributor.authorAmire, Niyaz
dc.contributor.authorAbdirassil, Aizat
dc.contributor.authorMulikova, Tomiris
dc.contributor.authorBegenov, Azamat
dc.contributor.authorKiesilä, Anniina
dc.contributor.authorPeshkov, Anatoly A.
dc.contributor.authorPeshkov, Vsevolod A.
dc.contributor.authorUtepbergenov, Darkhan
dc.date.accessioned2024-03-20T12:16:31Z
dc.date.available2024-03-20T12:16:31Z
dc.date.issued2024
dc.identifier.citationYedigenov, M., Amire, N., Abdirassil, A., Mulikova, T., Begenov, A., Kiesilä, A., Peshkov, A. A., Peshkov, V. A., & Utepbergenov, D. (2024). Glyoxalase-based toolbox for the enantioselective synthesis of α-hydroxy carboxylic acids. <i>Organic and Biomolecular Chemistry</i>, <i>Advance Article</i>. <a href="https://doi.org/10.1039/D3OB02098C" target="_blank">https://doi.org/10.1039/D3OB02098C</a>
dc.identifier.otherCONVID_207171021
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/93987
dc.description.abstractWe report highly enantioselective synthesis of L-α-hydroxy carboxylic acids (L-αHCAs) via enzymatic intramolecular Cannizzaro reaction of (hetero)aryl glyoxals in the presence of glutathione-independent human glyoxalase DJ-1. Combined with the optimized synthesis of D-αHCAs using glyoxalases I and II, this approach offers a general, scalable and operationally simple access to both enantiomers of α-hydroxy acids in moderate to excellent yields with uniformly high enantioselectivity.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherRoyal Society of Chemistry
dc.relation.ispartofseriesOrganic and Biomolecular Chemistry
dc.rightsIn Copyright
dc.subject.otherglyoksalaasi
dc.subject.otherglyoxalase
dc.titleGlyoxalase-based toolbox for the enantioselective synthesis of α-hydroxy carboxylic acids
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202403202526
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn1477-0520
dc.relation.volumeAdvance Article
dc.type.versionacceptedVersion
dc.rights.copyright© 2024 Royal Society of Chemistry
dc.rights.accesslevelembargoedAccessfi
dc.subject.ysoorgaaninen kemia
dc.subject.ysosynteesi
dc.subject.ysoentsyymit
dc.subject.ysokarboksyylihapot
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p11902
jyx.subject.urihttp://www.yso.fi/onto/yso/p8467
jyx.subject.urihttp://www.yso.fi/onto/yso/p4769
jyx.subject.urihttp://www.yso.fi/onto/yso/p27282
dc.rights.urlhttp://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi10.1039/D3OB02098C
jyx.fundinginformationThis work was supported by Nazarbayev University CRP grant 091019CRP2121 to D. U. and FDCRGP grant 11022021FD2903 to V. P.
dc.type.okmA1


Aineistoon kuuluvat tiedostot

Thumbnail

Aineisto kuuluu seuraaviin kokoelmiin

Näytä suppeat kuvailutiedot

In Copyright
Ellei muuten mainita, aineiston lisenssi on In Copyright