Please use this identifier to cite or link to this item: https://doi.org/10.1021/cs300313j
DC FieldValue
dc.titleEnantioselective organocatalytic conjugate addition of nitroalkanes to electrophilic 2-iminochromenes
dc.contributor.authorLi, W.
dc.contributor.authorLiu, H.
dc.contributor.authorJiang, X.
dc.contributor.authorWang, J.
dc.date.accessioned2014-06-23T05:38:37Z
dc.date.available2014-06-23T05:38:37Z
dc.date.issued2012-08-03
dc.identifier.citationLi, W., Liu, H., Jiang, X., Wang, J. (2012-08-03). Enantioselective organocatalytic conjugate addition of nitroalkanes to electrophilic 2-iminochromenes. ACS Catalysis 2 (8) : 1535-1538. ScholarBank@NUS Repository. https://doi.org/10.1021/cs300313j
dc.identifier.issn21555435
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76105
dc.description.abstractWe disclose a new efficient enantioselective organocatalytic conjugate addition method for the preparation of 2-amino-4H-chromenes in high to excellent yields (75-95%) and with high to excellent enantioselectivities (86-97% ee). It is noteworthy that the 2-iminochromene was first disclosed as an active electrophile. © 2012 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/cs300313j
dc.sourceScopus
dc.subject2-amino-4H-chromenes
dc.subjectconjugate addition
dc.subjectnitroalkane
dc.subjectorganocatalysis
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/cs300313j
dc.description.sourcetitleACS Catalysis
dc.description.volume2
dc.description.issue8
dc.description.page1535-1538
dc.identifier.isiut000307257800002
Appears in Collections:Staff Publications

Show simple item record
Files in This Item:
There are no files associated with this item.

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.