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Reserpine analogues: III. Alkoxy-β-phenylethylamine derivatives

✍ Scribed by T. Kralt; W. J. Asma; H. D. Moed

Book ID
104586316
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
451 KB
Volume
80
Category
Article
ISSN
0165-0513

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✦ Synopsis

Abstract

The synthesis of a series of compounds resembling in some respects the reserpine alkaloid and containing a β‐phenylethylamine configuration substituted at the phenyl group with alkoxyl groups is described.

📜 SIMILAR VOLUMES

Reserpine analogues IV. Hydroxy-β-phenyl
Reserpine analogues IV. Hydroxy-β-phenylethylamine derivatives
✍ T. Kralt; W. J. Asma; H. D. Moed 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 496 KB

## Abstract The synthesis of a series of compounds resembling in some respects the reserpine alkaloid and containing a β‐phenylethylamine configuration substituted at the phenylgroup with hydroxyl groups is described.

Reserpine analogues: I. β-Indolylethylam
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## Abstract The synthesis of a series of compounds resembling in some respects the alkaloid reserpine is described. The compounds are β‐indolylethylamine (tryptamine) derivatives.

Assignment of 15N-NMR resonances of vita
Assignment of 15N-NMR resonances of vitamin B12 analogues by 2D-[15N, 1H] long-range correlation: Fully [15N]-labelled Co-β-cyano-5-hydroxybenzimidazoylcobamide (factor III) and derivatives
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## Abstract The ^15^N‐NMR spectra of vitamin B~12~ analogues obtained in fully ^15^N‐labelled form have been measured by direct and inverse (^15^N, ^1^H) correlated spectroscopy. All resonances, except those of the NH~2~ groups, have been assigned to individual N‐atoms. The influences on δ (N) are