ChemInform Abstract: A <sup>15</sup>NMR Study of the Acid‐Base and Tautomeric Equilibria of 4‐Substituted Imidazoles and Its Relevance to the Catalytic Mechanism of α‐Lytic Protease (z.B. von Histamin oder Imidazol‐4‐essigsäure; pH‐Abhängigkeit).

Roberts, John D.; Yu, Chengbin; Flanagan, C.; Birdseye, Teresa R.

doi:10.1002/chin.198243093

Chemischer Informationsdienst

1982

DOI: 10.1002/chin.198243093

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ChemInform Abstract: A ¹⁵NMR Study of the Acid‐Base and Tautomeric Equilibria of 4‐Substituted Imidazoles and Its Relevance to the Catalytic Mechanism of α‐Lytic Protease (z.B. von Histamin oder Imidazol‐4‐essigsäure; pH‐Abhängigkeit).

John D. Roberts¹,

Chengbin Yu²,

C. Flanagan³

et al.

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ChemInform Abstract: A ¹⁵NMR Study of the Acid‐Base and Tautomeric Equilibria of 4‐Substituted Imidazoles and Its Relevance to the Catalytic Mechanism of α‐Lytic Protease (z.B. von Histamin oder Imidazol‐4‐essigsäure; pH‐Abhängigkeit).

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ChemInform Abstract: A 15NMR Study of the Acid‐Base and Tautomeric Equilibria of 4‐Substituted Imidazoles and Its Relevance to the Catalytic Mechanism of α‐Lytic Protease (z.B. von Histamin oder Imidazol‐4‐essigsäure; pH‐Abhängigkeit).

Cited by 0 publications

References 1 publication

No citations

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About

ChemInform Abstract: A ¹⁵NMR Study of the Acid‐Base and Tautomeric Equilibria of 4‐Substituted Imidazoles and Its Relevance to the Catalytic Mechanism of α‐Lytic Protease (z.B. von Histamin oder Imidazol‐4‐essigsäure; pH‐Abhängigkeit).