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Overcoming NMR line broadening of nitrogen containing compounds: A simple solution.
Ma, Junhe; Ye, Qingmei; Green, Rebecca A; Gurak, John; Ayers, Sloan; Huang, Yande; Miller, Scott A.
Affiliation
  • Ma J; Chemical Process Development, Bristol Myers Squibb Company, New Brunswick, New Jersey, USA.
  • Ye Q; Chemical Process Development, Bristol Myers Squibb Company, New Brunswick, New Jersey, USA.
  • Green RA; Chemical Process Development, Bristol Myers Squibb Company, New Brunswick, New Jersey, USA.
  • Gurak J; Chemical Process Development, Bristol Myers Squibb Company, New Brunswick, New Jersey, USA.
  • Ayers S; Chemical Process Development, Bristol Myers Squibb Company, New Brunswick, New Jersey, USA.
  • Huang Y; Chemical Process Development, Bristol Myers Squibb Company, New Brunswick, New Jersey, USA.
  • Miller SA; Chemical Process Development, Bristol Myers Squibb Company, New Brunswick, New Jersey, USA.
Magn Reson Chem ; 62(3): 198-207, 2024 Mar.
Article in En | MEDLINE | ID: mdl-38258438
ABSTRACT
This study presents a straightforward solution to the challenge of elucidating the structures of nitrogen containing compounds undergoing isomerization. When spectral line broadening occurs related to isomerization, be it prototropic tautomerism or bond rotations, this poses a significant obstacle to structural elucidation. By adding acids, we demonstrate a simple approach to overcome this issue and effectively sharpen NMR signals for acid stable prototropic tautomers as well as the conformational isomers containing a morpholine or piperazine ring.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Magn Reson Chem Journal subject: QUIMICA Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Magn Reson Chem Journal subject: QUIMICA Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Reino Unido