The vicinal difluoro motif: The synthesis and conformation of erythro- and threo- diastereoisomers of 1,2-difluorodiphenylethanes, 2,3-difluorosuccinic acids and their derivatives-Reference-Cited by-同舟云学术

The vicinal difluoro motif: The synthesis and conformation of erythro- and threo- diastereoisomers of 1,2-difluorodiphenylethanes, 2,3-difluorosuccinic acids and their derivatives

Published:2006-10-02 Issue: Volume:2 Page:
ISSN:1860-5397
Container-title:Beilstein Journal of Organic Chemistry
language:en
Short-container-title:Beilstein J. Org. Chem.

Author:

O'Hagan David,Rzepa Henry S,Schüler Martin,Slawin Alexandra M Z

Publisher

Beilstein Institut

Subject

Organic Chemistry

Link

https://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-2-19.pdf

Reference31 articles.

1. Contribution to the Study of the Gauche Effect. The Complete Structure of the Anti Rotamer of 1,2-Difluoroethane

2. Conformation in 2,3-difluorobutanes

3. The fluorine gauche effect. Langmuir isotherms report the relative conformational stability of (±)-erythro- and (±)-threo-9,10-difluorostearic acidsElectronic supplementary information (ESI) available: characterisation of compounds 4, 5, 7–9, 11–13. See http://www.rsc.org/suppdata/cc/b2/b202891c/

4. The Polar Fluorination of Propenylbenzene

5. Reactions of Olefins with Xenon Fluorides

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