Comparison of Dynamic HPLC and Dynamic NMR in the Study of Conformational Stereodynamics: Case of the Enantiomers of a Hindered Secondary Phosphine Oxide1-Reference-Cited by-同舟云学术

Comparison of Dynamic HPLC and Dynamic NMR in the Study of Conformational Stereodynamics: Case of the Enantiomers of a Hindered Secondary Phosphine Oxide1

Published:2000-04-29 Issue:19 Volume:122 Page:4776-4780
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Gasparrini F.¹,Lunazzi L.¹,Mazzanti A.¹,Pierini M.¹,Pietrusiewicz K. M.¹,Villani C.¹

Affiliation:

1. Contribution from the Dipartimento di Studi di Chimica e Tecnologia delle Sostanze Biologicamente Attive, Università “La Sapienza”, P.ale Aldo Moro, 5 Roma, 00185 Italy, Department of Organic Chemistry “A. Mangini”, University of Bologna, Risorgimento 4, Bologna, 40136 Italy, Department of Organic Chemistry, Maria Curie-Sklodowska University, Lublin and Institute of Organic Chemistry, Polish Academy of Sciences, Warsaw, Poland, and Dipartimento Scienze del Farmaco, Università “G. D'Annunzio”, via dei...

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9941779

Reference13 articles.

1. Organic Stereochemistry and Conformational Analysis from Enantioselective Chromatography and Dynamic Nuclear Magnetic Resonance Measurements

2. Conformational studies by dynamic NMR. 50. Atropisomerism in hindered naphthyl sulfoxides: structure, stereodynamics, and chiral resolution

3. Conformational Assignment, Absolute Configuration, and Chiral Separation of All the Stereoisomers Created by the Combined Presence of Stereogenic Centers and Stereogenic Conformational Axes in a Highly Hindered 1,5-Naphthyl Sulfoxide

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