Sulfonylhalogenidy (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sulfonylhalogenidy" in Czech language version.

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Magdolna Hargittai; István Hargittai. On the molecular structure of methane sulfonyl chloride as studied by electron diffraction. The Journal of Chemical Physics. 1973, s. 2513. DOI 10.1063/1.1680366. Bibcode 1973JChPh..59.2513H.
H. J. Lehmler. Synthesis of environmentally relevant fluorinated surfactants—a review. Chemosphere. 2005, s. 1471–1496. DOI 10.1016/j.chemosphere.2004.11.078. PMID 15694468. Bibcode 2005Chmsp..58.1471L.
Arjun Narayanan; Lyn H. Jones. Sulfonyl fluorides as privileged warheads in chemical biology. Chemical Science. 2015, s. 2650–2659. DOI 10.1039/C5SC00408J. PMID 28706662.
α-Haloalkanesulfonyl Bromides in Organic Synthesis. 5. Versatile Reagents for the Synthesis of Conjugated Polyenes, Enones and 1,3-Oxathiole 1,1-Dioxides. Journal of the American Chemical Society. 1986, s. 4568–4580. DOI 10.1021/ja00275a051.
W.-Y. Huang; L.-Q. Hu. The chemistry of perfluoroalkanesulfonyl iodides. Journal of Fluorine Chemistry. 1989, s. 25–44. DOI 10.1016/S0022-1139(00)84369-9.
V. Percec; C. Grigoras. Arenesulfonyl iodides: The third universal class of functional initiators for the metal-catalyzed living radical polymerization of methacrylates and styrenes. Journal of Polymer Science Part A: Polymer Chemistry. 2005, s. 3920–3931. DOI 10.1002/pola.20860. Bibcode 2005JPoSA..43.3920P.

Magdolna Hargittai; István Hargittai. On the molecular structure of methane sulfonyl chloride as studied by electron diffraction. The Journal of Chemical Physics. 1973, s. 2513. DOI 10.1063/1.1680366. Bibcode 1973JChPh..59.2513H.
H. J. Lehmler. Synthesis of environmentally relevant fluorinated surfactants—a review. Chemosphere. 2005, s. 1471–1496. DOI 10.1016/j.chemosphere.2004.11.078. PMID 15694468. Bibcode 2005Chmsp..58.1471L.
V. Percec; C. Grigoras. Arenesulfonyl iodides: The third universal class of functional initiators for the metal-catalyzed living radical polymerization of methacrylates and styrenes. Journal of Polymer Science Part A: Polymer Chemistry. 2005, s. 3920–3931. DOI 10.1002/pola.20860. Bibcode 2005JPoSA..43.3920P.

H. J. Lehmler. Synthesis of environmentally relevant fluorinated surfactants—a review. Chemosphere. 2005, s. 1471–1496. DOI 10.1016/j.chemosphere.2004.11.078. PMID 15694468. Bibcode 2005Chmsp..58.1471L.
Arjun Narayanan; Lyn H. Jones. Sulfonyl fluorides as privileged warheads in chemical biology. Chemical Science. 2015, s. 2650–2659. DOI 10.1039/C5SC00408J. PMID 28706662.

ADAMS, Roger; MARVEL, C. S.; CLARKE, H. T.; BABCOCK, G. S.; MURRAY, T. F. Benzenesulfonyl chloride. Org. Synth.. 1921, s. 21. Dostupné online. ; Coll. Vol.. S. 84.
BLOCK, E.; ASLAM, M. A General Synthetic Method for the Preparation of Conjugated Dienes from Olefins using Bromomethanesulfonyl Bromide: 1,2-Dimethylenecyclohexane. Org. Synth.. 1993. Dostupné online. ; Coll. Vol.. S. 212.