Stereomutation of Conformational Enantiomers of 9-Isopropyl-9-formylfluorene and Related Acyl Derivatives-Reference-Cited by-同舟云学术

Stereomutation of Conformational Enantiomers of 9-Isopropyl-9-formylfluorene and Related Acyl Derivatives

Published:2008-07-22 Issue:16 Volume:73 Page:6382-6385
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Casarini Daniele¹,Lunazzi Lodovico¹,Mazzanti Andrea¹

Affiliation:

1. Department of Chemistry, University of Basilicata, via N. Sauro 85, Potenza 85100, Italy, and Department of Organic Chemistry “A. Mangini”, University of Bologna, Viale Risorgimento 4, Bologna 40136, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo8008897

Reference31 articles.

1. Oki, M.Applications of Dynamic NMR Spectroscopy to Organic Chemistry; VCH Publisher: Deerfield Beach, FL, 1985, 211

2. Rotational isomerism in fluorene derivatives. XX. Conformational equilibria of 9-substituted 9-(o-methylthiomethylphenyl)- and 9-substituted 9-(o-methylsulfinylmethylphenyl)fluorenes

4. Structure-activity relationship studies in the field of calcium(II) antagonists. Effect of modifications at the tetrasubstituted carbon of verapamil-like compounds

5. As often observed in conformational processes, the free energy of activation was found independent of temperature within the errors, indicating a negligible value of ΔS≠. See, for instance:

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