ChemInform Abstract: Conformational Behavior on 2,2,3-Trisubstituted 1,2,3,4-Tetrahydroquinoline Alkaloids, Virantmycin, Benzastatins, and Their Congeners, Evaluated by Semi-Empirical Molecular Orbital Calculations.

Conformational behavior on 2,2,3-trisubs

Conformational behavior on 2,2,3-trisubstituted 1,2,3,4-tetrahydroquinoline alkaloids, virantmycin, benzastatins, and their congeners, evaluated by semi-empirical molecular orbital calculations

✍ Yoshiki Morimoto 📂 Article 📅 1998 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 412 KB

## Abstract The conformational behaviors on ring inversion between two half‐chair conformers a and b in physiologically active 2,2,3‐trisubstituted 1,2,3,4‐tetrahydroquinoline alkaloids, virantmycin (1), benzastatin C (6), benzastatin D (7), and their congeners 2–5, which were revealed by their nmr