Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/155331
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dc.contributor.authorXie, Peizhongen_US
dc.contributor.authorSun, Zuolianen_US
dc.contributor.authorLi, Shuangshuangen_US
dc.contributor.authorCai, Xinyingen_US
dc.contributor.authorQiu, Juen_US
dc.contributor.authorFu, Weishanen_US
dc.contributor.authorGao, Cuiqingen_US
dc.contributor.authorWu, Shishengen_US
dc.contributor.authorYang, Xiaoboen_US
dc.contributor.authorLoh, Teck-Pengen_US
dc.date.accessioned2022-03-18T06:07:27Z-
dc.date.available2022-03-18T06:07:27Z-
dc.date.issued2020-
dc.identifier.citationXie, P., Sun, Z., Li, S., Cai, X., Qiu, J., Fu, W., Gao, C., Wu, S., Yang, X. & Loh, T. (2020). Reciprocal-activation strategy for allylic sulfination with unactivated allylic alcohols. Organic Letters, 22(12), 4893-4897. https://dx.doi.org/10.1021/acs.orglett.0c01747en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttps://hdl.handle.net/10356/155331-
dc.description.abstractA reciprocal-activation strategy for allylic sulfination with unactivated allylic alcohols was developed. In this reaction, the hydrogen bond interaction between allylic alcohols and sulfinic acids allowed for reciprocal activation, which enabled a dehydrative cross-coupling process to occur under mild reaction conditions. This reaction worked in an environmentally friendly manner, yielding water as the only byproduct. A variety of allylic sulfones could be obtained in good to excellent yields with wide functional group tolerance. In gram scale reactions, allylic sulfones could be conveniently isolated in high yield by filtration.en_US
dc.description.sponsorshipMinistry of Education (MOE)en_US
dc.language.isoenen_US
dc.relation2016-T1-002-043en_US
dc.relationRG111/16en_US
dc.relation.ispartofOrganic Lettersen_US
dc.rights© 2020 American Chemical Society. All rights reserved.en_US
dc.subjectScience::Chemistryen_US
dc.titleReciprocal-activation strategy for allylic sulfination with unactivated allylic alcoholsen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doi10.1021/acs.orglett.0c01747-
dc.identifier.pmid32496788-
dc.identifier.scopus2-s2.0-85086584379-
dc.identifier.issue12en_US
dc.identifier.volume22en_US
dc.identifier.spage4893en_US
dc.identifier.epage4897en_US
dc.subject.keywordsReciprocal-Activation Strategyen_US
dc.subject.keywordsAllylic Sulfinationen_US
dc.description.acknowledgementThe authors gratefully acknowledge the financial support from the National Natural Science Foundation of China (21702108), the Natural Science Foundation of Jiangsu Province, China (BK20160977), the Six Talent Peaks Project gsu Province (YY-033), Grant MOE2016-T1-002-043 (RG111/16) from the Ministry of Education of Singapore, and Nanjing Tech University (39837101).en_US
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item.fulltextNo Fulltext-
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