Teitl: Data underpinning "N-Cyanation of Secondary Amines using Trichloroacetonitrile"


Dyfyniad
Ayres JN, Ling KB, Morrill LC (2016). Data underpinning "N-Cyanation of Secondary Amines using Trichloroacetonitrile". Cardiff University. https://doi.org/10.17035/d.2016.0011295237



Hawliau Mynediad: Gall data fod ar gael yn rhad ac am ddim yn amodol ar briodoli

Dull Mynediad: I anfon cais i gael y data hwn, ebostiwch opendata@caerdydd.ac.uk


Crewyr y Set Ddata o Brifysgol Caerdydd


Manylion y Set Ddata

Cyhoeddwr: Cardiff University

Dyddiad (y flwyddyn) pryd y daeth y data ar gael i'r cyhoedd: 2016

Fformat y data: .txt, .inmr, .info, .par, .xml, .pdf, .temp, .back, .jpg, .ispd

Meddalwedd ofynnol: An appropriate NMR processing software is require for raw NMR data files.

Amcangyfrif o gyfanswm maint storio'r set ddata: Llai na 100 megabeit

Nifer y ffeiliau yn y set ddata: 1608

DOI : 10.17035/d.2016.0011295237

DOI URL: http://doi.org/10.17035/d.2016.0011295237

Related URL: http://blogs.cardiff.ac.uk/themorrillgroup/


Disgrifiad

A one-pot N-cyanation of secondary amines has been developed using trichloroacetonitrile as an inexpensive cyano source. A diverse range of cyclic and acyclic secondary amines can be readily transformed into the corresponding cyanamides in good isolated yields, with the method successfully utilised in the final synthetic step of a biologically-active rolipram-derived cyanamide. This approach exhibits distinct selectivity when compared to the use of highly toxic cyanogen bromide.

Herein we include all underpinning data for this publication, including:

1H, 19F and 13C NMR raw data files
IR spectra
HRMS spectra

Research results based upon these data are published at http://10.1021/acs.orglett.6b02775


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Diweddarwyd y tro diwethaf ar 2022-29-04 am 14:42