Teitl: Manganese-Catalyzed N-Alkylation of Sulfonamides Using Alcohols


Dyfyniad
Reed-Berendt BG, Morrill LC (2019). Manganese-Catalyzed N-Alkylation of Sulfonamides Using Alcohols. Cardiff University. http://doi.org/10.17035/d.2019.0069100566



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: 2019

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

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

Amcangyfrif o gyfanswm maint storio'r set ddata: Llai nag 1 gigabeit

Nifer y ffeiliau yn y set ddata: 2773

DOI : 10.17035/d.2019.0069100566

DOI URL: http://doi.org/10.17035/d.2019.0069100566

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


Disgrifiad

An efficient manganese-catalyzed N-alkylation of sulfonamides has been developed. This borrowing hydrogen approach employs a well-defined and bench stable Mn(I) PNP pincer precatalyst, allowing benzylic and simple primary aliphatic alcohols to be employed as alkylating agents. A diverse range of aryl and alkyl sulfonamides undergoes mono-N-alkylation in excellent isolated yields (32 examples, 85% average yield).

Analysis of reaction products from this methodology resulted in the following data:

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

IR spectra

High-Resolution Mass Spectrography spectra.

Research results based upon these data are published at http://doi.org/10.1021/acs.joc.9b00203


Meysydd Ymchwil

Prosiectau Cysylltiedig

Diweddarwyd y tro diwethaf ar 2019-02-07 am 11:10