dc.contributor.author | Thomas, Annu Anna | |
dc.contributor.author | Nagamalla, Someshwar | |
dc.contributor.author | Sathyamoorthi, Shyam | |
dc.date.accessioned | 2021-12-22T20:24:01Z | |
dc.date.available | 2021-12-22T20:24:01Z | |
dc.date.issued | 2020-07-21 | |
dc.identifier.citation | Thomas, A. A., Nagamalla, S., & Sathyamoorthi, S. (2020). Salient features of the aza-Wacker cyclization reaction. Chemical science, 11(31), 8073–8088. https://doi.org/10.1039/d0sc02554b | en_US |
dc.identifier.uri | http://hdl.handle.net/1808/32305 | |
dc.description.abstract | The intramolecular aza-Wacker reaction has unparalleled potential for the site-selective amination of olefins, but it is perhaps underappreciated relative to other alkene oxidations. The first part of this review makes the distinction between classical and tethered aza-Wacker cyclization reactions and summarizes examples of the latter. The second portion focuses on developments in asymmetric aza-Wacker cyclization technology. The final part of the review summarizes applications of all classes of aza-Wacker cyclization reactions to natural product assembly. | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.rights | © The Royal Society of Chemistry 2020. This work is licensed under a Creative Commons Attribution 4.0 International License. | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | en_US |
dc.title | Salient features of the aza-Wacker cyclization reaction | en_US |
dc.type | Article | en_US |
kusw.kuauthor | Thomas, Annu Anna | |
kusw.kuauthor | Nagamalla, Someshwar | |
kusw.kuauthor | Sathyamoorthi, Shyam | |
kusw.kudepartment | Medicinal Chemistry | en_US |
dc.identifier.doi | 10.1039/d0sc02554b | en_US |
dc.identifier.orcid | https://orcid.org/ 0000-0003-4705-7349 | en_US |
kusw.oaversion | Scholarly/refereed, publisher version | en_US |
kusw.oapolicy | This item meets KU Open Access policy criteria. | en_US |
dc.identifier.pmid | PMC8163389 | en_US |
dc.rights.accessrights | openAccess | en_US |