NMR study on 9‐S and 9‐R oxirane derivatives of ascomycin
Kathrin Baumann, Klemens Högenauer, Gerhard Schulz, Andrea Steck
Abstract
Kathrin Baumann, Klemens Högenauer, Gerhard Schulz, Andrea Steck
Abstract
Abstract Structure elucidation of 9‐S and 9‐R oxirane derivatives of ascomycin, a 23‐membered immunomodulating macrolactam, was performed using NMR spectroscopy. The total 1H and 13C signal assignments required the gradient‐selected versions of COSY (gs‐COSY), heteronuclear multiple quantum‐correlation spectroscopy (gs‐HSQC), heteronuclear multiple‐bond correlation spectroscopy (gs‐HMBC), and nuclear Overhauser methods. The data sets then were used to examine the dependence of ketone–hemiketal and cis–trans amide equilibria on the substitution pattern and the absolute configuration of the chiral oxirane. Copyright © 2002 John Wiley & Sons, Ltd.
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Abstract Structure elucidation of 9‐S and 9‐R oxirane derivatives of ascomycin, a 23‐membered immunomodulating macrolactam, was performed using NMR spectroscopy. The total 1H and 13C signal assignments required the gradient‐selected versions of COSY (gs‐COSY), heteronuclear multiple quantum‐correlation spectroscopy (gs‐HSQC), heteronuclear multiple‐bond correlation spectroscopy (gs‐HMBC), and nuclear Overhauser methods. The data sets then were used to examine the dependence of ketone–hemiketal and cis–trans amide equilibria on the substitution pattern and the absolute configuration of the chiral oxirane. Copyright © 2002 John Wiley & Sons, Ltd.
Key concepts: Heteronuclear molecule, Chemistry, Heteronuclear single quantum coherence spectroscopy, Two-dimensional nuclear magnetic resonance spectroscopy, Stereochemistry, Nuclear Overhauser effect, Nuclear magnetic resonance spectroscopy, Amide