A Mild and Efficient Method for the Syntheses and Regioselective Ring-Opening of Aziridines

Please use this identifier to cite or link to this item: http://hdl.handle.net/10995/102748

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. Зырянов, Г. В.
Issue Date:	2017
Publisher:	Georg Thieme Verlag
Citation:	A Mild and Efficient Method for the Syntheses and Regioselective Ring-Opening of Aziridines / N. C. Ghosal, S. Mahato, R. Chatterjee, et al. — DOI 10.1055/s-0036-1588809 // SynOpen. — 2017. — Vol. 1. — Iss. 1. — P. 15-23. — so-2017-d0008-op.
Abstract:	We have developed a new synthetic method for the synthesis of aziridines using Chloramine-T as an effective reagent in the presence of NH 2OH·HCl and NaIO 4. We found that the same combination of NH 2OH·HCl and NaIO 4is also very effective for nucleophilic ring opening of aziridines. Copyright © 2017 Georg Thieme Verlag Stuttgart · New York.
Keywords:	AMINOIODIDE AZIRIDINES DIFUNCTIONALIZATION IN SITU GENERATED IODINE ROOM TEMPERATURE
URI:	http://hdl.handle.net/10995/102748
Access:	info:eu-repo/semantics/openAccess
SCOPUS ID:	85049278770
PURE ID:	9077088
ISSN:	25099396
DOI:	10.1055/s-0036-1588809
Appears in Collections:	Научные публикации, проиндексированные в SCOPUS и WoS CC

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