Structural and conformational analysis by1H NMR and13C NMR of a new angiotensin I converting enzyme inhibitor, thetert-butylamine salt of (2S)-2-[(1S)-1-carbethoxybutylamino]-1-oxopropyl-(2S, 3aS, 7aS) perhydroindole-2-carboxylic acid (perindopril)-Reference-Cited by-同舟云学术

Structural and conformational analysis by1H NMR and13C NMR of a new angiotensin I converting enzyme inhibitor, thetert-butylamine salt of (2S)-2-[(1S)-1-carbethoxybutylamino]-1-oxopropyl-(2S, 3aS, 7aS) perhydroindole-2-carboxylic acid (perindopril)

Published:1988-04 Issue:4 Volume:26 Page:296-302
ISSN:0749-1581
Container-title:Magnetic Resonance in Chemistry
language:en
Short-container-title:Magn. Reson. Chem.

Author:

Platzer N.,Bouchet J. P.,Volland J. P.

Publisher

Wiley

Subject

General Materials Science,General Chemistry

Reference33 articles.

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4. Synthesis and structure activity relationships of potent new angiotensin converting enzyme inhibitors containing saturated bicyclic amino acids

5. and J. Chem. Soc., Perkin Trans. 1 155 (1984).

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