Conformational Pseudopolymorphism and Solid-State CPMAS NMR Studies for Determination of Solvent-Dependent Solution-State Conformational Preferences for (−)-Scopolamine Hydrobromide/Hydrochloride Salts-Reference-Cited by-同舟云学术

Conformational Pseudopolymorphism and Solid-State CPMAS NMR Studies for Determination of Solvent-Dependent Solution-State Conformational Preferences for (−)-Scopolamine Hydrobromide/Hydrochloride Salts

Published:1999-11-23 Issue:25 Volume:64 Page:9217-9224
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Glaser Robert¹,Shiftan Dror¹,Drouin Marc²

Affiliation:

1. Department of Chemistry, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel

2. Département de Chimie, Université de Sherbrooke, Québec, Canada J1K 2R1

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9912956

Reference36 articles.

1. The Merck Index, 12th ed.; Budavari, S., Ed.; Merck: Rahway, NJ, 1996; p 1444 and references therein.

2. 632. The stereochemistry of the tropane alkaloids. Part XIV. The absolute configuration of (–)-tropic acid, hyoscyamine, and hyoscine

3. Stereochemistry of the N-methyl group in salts of tropane alkaloids

4. Spectral reassignment and structure elucidation of scopolamine free base through two-dimensional NMR techniques

5. NMR and molecular mechanics studies on the solution-state conformation of (−)-scopolamine free base

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