A mechanistic insight into the boron-catalysed direct amidation reaction. NMR spectra.

DOI: 10.14469/hpc/2247 Metadata

Created: 2017-03-15 10:28

Last modified: 2020-06-01 18:01

Author: Henry Rzepa

License: Creative Commons: Public Domain Dedication 1.0

Funding: (none given)

Co-author: Andrew Whiting
Co-author: Marco Sabatini
Co-author: Sergey Arkhipenko
Co-author: Tom Sheppard

Description

Complete NMR data for selected compounds.. Version 11 or higher of the Mestrenova software is required to process these files, available from http://mestrelab.com/software/mnova/download/ Download the .mnpub signature file and load it into MestreNova to view the spectra. To view datasets obtained here, Mestrenova need not be licensed.

Member of collection / collaboration

DOIDescription
10.14469/hpc/1620 A mechanistic insight into the boron-catalysed direct amidation reaction

Members

DOIDescription
10.14469/hpc/2366 11a. (benzylamino)bis(3,4,5-trifluorophenyl)-λ4-boraneyl 4-phenylbutanoate
10.14469/hpc/2371 9b. 2,2-bis(3,4,5-trifluorophenyl)-1,3,2λ4-oxazaborolidine - ethanolamine complex.
10.14469/hpc/2376 10a. N-benzyl-1-hydroxy-1,1-bis(3,4,5-trifluorophenyl)-λ4-boranaminium
10.14469/hpc/2367 16d. Two mols of phenylmethanamine + 2,4,6-triphenyl-1,3,5,2,4,6-trioxatriborinane
10.14469/hpc/2372 9b. hydroxybis(3,4,5-trifluorophenyl)borane
10.14469/hpc/2377 11b. (benzylamino)bis(3,4,5-trifluorophenyl)-λ4-boraneyl benzoate
10.14469/hpc/2380 16a. N-benzyl-2,4,6-tris(3,4,5-trifluorophenyl)-1,3,5,2λ4,4,6-trioxatriborinan-2-aminium
10.14469/hpc/2368 16c. 4 mols of phenylmethanamine + 2,4,6-triphenyl-1,3,5,2,4,6-trioxatriborinane
10.14469/hpc/2373 9c. 2,2-bis(2-chlorophenyl)-1,3,2λ4-oxazaborolidine - ethanolamine complex
10.14469/hpc/2378 11c. (benzylamino)diphenyl-λ4-boraneyl benzoate
10.14469/hpc/2381 17a. (1r,5r)-3,7-dibenzyl-1,5-bis(2-chlorophenyl)-2λ3,4,6,8λ3,9-pentaoxa-1λ4,5λ4-diborabicyclo[3.3.1]nona-2,7-diene
10.14469/hpc/2374 9c. bis(2-chlorophenyl)(hydroxy)borane
10.14469/hpc/2370 9a. 2,2-diphenyl-1,3,2λ4-oxazaborolidine
10.14469/hpc/2369 9a. 2,2-diphenyl-1,3,2λ4-oxazaborolidine - ethanolamine complex
10.14469/hpc/2375 10b. ((2-aminoethyl)-λ4-azaneyl)(hydroxy)bis(3,4,5-trifluorophenyl)borate
10.14469/hpc/2379 11d. (benzylamino)bis(2-chlorophenyl)-λ4-boraneyl 4-phenylbutanoate
10.14469/hpc/2382 17b. (1r,5r)-3,7-dibenzyl-1,5-bis(2-iodophenyl)-2λ3,4,6,8λ3,9-pentaoxa-1λ4,5λ4-diborabicyclo[3.3.1]nona-2,7-diene
10.14469/hpc/2753 Phenylacetic acid and benzylamine amidation catalysed by Borinic acid
10.14469/hpc/2754 Phenylacetic acid and benzylamine amidation catalysed by Boronic acid
10.14469/hpc/3285 (2-chlorophenyl)boronic acid
10.14469/hpc/3286 2-(benzylamino)-2-(2-chlorophenyl)-5-phenyl-1,3,2λ4-dioxaborolan-4-one
10.14469/hpc/3287 2-(benzylamino)-2,5-diphenyl-1,3,2λ4-dioxaborolan-4-one
10.14469/hpc/3288 2,4,6-tris(2-chlorophenyl)-1,3,5,2,4,6-trioxatriborinane
10.14469/hpc/3289 3,7-dibenzyl-1,5-bis(2-chlorophenyl)-2λ3,4,6λ3,8,9-pentaoxa-1λ4,5λ4-diborabicyclo[3.3.1]nona-2,6-diene
10.14469/hpc/2365 16b. 2-((2-aminoethyl)-λ4-azaneyl)-2,4,6-tris(3,4,5-trifluorophenyl)-1,3,5,2,4,6-trioxatriborinan-2-uide

Associated DOIs

Current dataset ...DOIDescription
isReferencedBy 10.14469/hpc/3702 Article: An Accessible Method for DFT Calculation of 11B NMR Shifts of Organoboron Compounds

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