Relevant bibliographies by topics / Article 8

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  1. Journal articles

Academic literature on the topic 'Article 8'

Author: Grafiati
Published: 4 June 2021
Last updated: 12 June 2025

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Journal articles on the topic "Article 8"

1

Zolten, Avram J., Kathryn Schlich, Michael P. Mozzoni, Yousef A. Fahoum, and John J. Chelonis. "Article 8." Archives of Physical Medicine and Rehabilitation 84, no. 10 (2003): E2. http://dx.doi.org/10.1016/j.apmr.2003.08.009.

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2

Nakase-Richardson, Risa, Stuart Yablon, and Mark Sherer. "Article 8." Archives of Physical Medicine and Rehabilitation 86, no. 10 (2005): e3. http://dx.doi.org/10.1016/j.apmr.2005.08.013.

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3

Stineman, M., A. E. Kurz, D. Kelleher, and B. Kennedy. "Article 8." Archives of Physical Medicine and Rehabilitation 87, no. 10 (2006): e3. http://dx.doi.org/10.1016/j.apmr.2006.07.011.

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4

Moreham, N. A. "VIOLATING ARTICLE 8." Cambridge Law Journal 66, no. 1 (2007): 35–37. http://dx.doi.org/10.1017/s0008197307000323.

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5

Tambuyzer, Erik. "Confusion over Article 8." EMBO reports 6, no. 8 (2005): 690. http://dx.doi.org/10.1038/sj.embor.7400485.

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6

Bandyopadhyay, Subir, and Mithilesh K. Pathak. "(158) Proposal to add a new article under Article 8." TAXON 59, no. 4 (2010): 1292. http://dx.doi.org/10.1002/tax.594038.

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7

Singh, Sarabjit. "Immigration and Article 8 Family Life." Judicial Review 15, no. 4 (2010): 377–81. http://dx.doi.org/10.5235/108546810794046412.

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8

Liddy, Jane. "Article 8: the pace of change." Northern Ireland Legal Quarterly 51, no. 3 (2020): 397–416. http://dx.doi.org/10.53386/nilq.v51i3.629.

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9

Refvik, Mitchell D., and Adrian L. Schwan. "Article." Canadian Journal of Chemistry 76, no. 2 (1998): 213–20. http://dx.doi.org/10.1139/v97-228.

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Abstract:
Lithium (E)-1-hexenesulfenate (5a) was treated with a number of TMS-X (TMS = trimethylsilyl) reagents to afford N,N-bis(trimethylsilyl)-(E)-1-hexenesulfenamide (7a) and (or) di((E)-1 hexenyl) disulfide (8), usually in low yield. The cleanest reactions, those from use of TMS-Cl (to afford 7a) and TMS-CN (which yields 8) were analyzed by variable temperature NMR. It was found that the low-temperature silylation reaction using TMS-Cl affords 7a and thiosulfinate 12 as initial products. Warming the mixture coerces the decomposition of 12. Treatment of 5a with TMS-CN also yields thiosulfinate 12 which is reduced to disulfide 8 as the temperature warms, possibly by action of cyanide ion. Evidence is presented that allows a confident structural assignment of the transient thiosulfinate 12, and mechanisms are suggested for the formation of 12. The study also led to the NMR observation of (E)-1-hexenesulfenate (5a).Key words: sulfenate, thiosulfinate, variable temperature NMR (VT NMR), silylation.
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10

Lambert, Suzanne, and Andrea Lindsay-Strugo. "Focus on Article 8 ECHR: Recent Developments." Judicial Review 13, no. 1 (2008): 29–40. http://dx.doi.org/10.1080/10854681.2008.11426542.

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