Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-019-10940-4
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dc.titlePractical access to axially chiral sulfonamides and biaryl amino phenols via organocatalytic atroposelective N-alkylation
dc.contributor.authorLu, S.
dc.contributor.authorNg, S.V.H.
dc.contributor.authorLovato, K.
dc.contributor.authorOng, J.-Y.
dc.contributor.authorPoh, S.B.
dc.contributor.authorNg, X.Q.
dc.contributor.authorKürti, L.
dc.contributor.authorZhao, Y.
dc.date.accessioned2021-12-09T02:57:24Z
dc.date.available2021-12-09T02:57:24Z
dc.date.issued2019
dc.identifier.citationLu, S., Ng, S.V.H., Lovato, K., Ong, J.-Y., Poh, S.B., Ng, X.Q., Kürti, L., Zhao, Y. (2019). Practical access to axially chiral sulfonamides and biaryl amino phenols via organocatalytic atroposelective N-alkylation. Nature Communications 10 (1) : 3061. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-019-10940-4
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/209889
dc.description.abstractThe importance of axial chirality in enantioselective synthesis has been widely recognized for decades. The practical access to certain structures such as biaryl amino phenols known as NOBINs in enantiopure form, however, still remains a challenge. In drug delivery, the incorporation of axially chiral molecules in systematic screening has also received a great deal of interest in recent years, which calls for innovation and practical synthesis of structurally different axially chiral entities. Herein we present an operationally simple catalytic N-alkylation of sulfonamides using commercially available chiral amine catalysts to deliver two important classes of axially chiral compounds: structurally diverse NOBIN analogs as well as axially chiral N-aryl sulfonamides in excellent enantiopurity. Structurally related chiral sulfonamide has shown great potential in drug molecules but enantioselective synthesis of them has never been accomplished before. The practical catalytic procedures of our methods also bode well for their wide application in enantioselective synthesis. © 2019, The Author(s).
dc.publisherNature Publishing Group
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2019
dc.typeArticle
dc.contributor.departmentDEPT OF CHEMISTRY
dc.description.doi10.1038/s41467-019-10940-4
dc.description.sourcetitleNature Communications
dc.description.volume10
dc.description.issue1
dc.description.page3061
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