Please use this identifier to cite or link to this item: http://hdl.handle.net/10995/74039
Title: A Mild and Efficient Method for the Syntheses and Regioselective Ring-Opening of Aziridines
Authors: Ghosal, N. C.
Mahato, S.
Chatterjee, R.
Santra, S.
Zyryanov, G. V.
Majee, A.
Issue Date: 2017
Publisher: Thieme Publishing Group
Citation: A Mild and Efficient Method for the Syntheses and Regioselective Ring-Opening of Aziridines / N. C. Ghosal, S. Mahato, R. Chatterjee // Synopen. — 2017. — Vol. 1. — Iss. 1. — P. 15-23.
Abstract: We have developed a new synthetic method for the synthesis of aziridines using Chloramine-T as an effective reagent in the presence of NH2OH center dot HCl and NaIO4. We found that the same combination of NH2OH center dot HCl and NaIO4 is also very effective for nucleophilic ring opening of aziridines.
URI: http://hdl.handle.net/10995/74039
metadata.dc.rights: cc-by
WOS ID: WOS:000457758900006
PURE ID: 9077088
ISSN: 2509-9396
DOI: 10.1055/s-0036-1588809
metadata.dc.description.sponsorship: This research was funded by the Russian Science Foundation, grant number 18-19-00090.
Appears in Collections:Научные публикации, проиндексированные в SCOPUS и WoS CC

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