Organic sulfide (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Organic sulfide" in English language version.

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books.google.com

Hellwinkel, Dieter (2012-12-06). Systematic Nomenclature of Organic Chemistry: A Directory to Comprehension and Application of its Basic Principles (1 ed.). Springer Science & Business Media. p. 131. ISBN 978-3-64256765-0. p. 131: Individual species of the genus thioether can again most uniformly be named as ...sulfane and ...sulfanyl derivatives, respectively (formerly: ...sulfides and ...thio derivatives, respectively). [...] Cyclic sulfides (thioethers) are treated as heterocycles, in the same way as their ether counterparts. Polysulfides substituted at both ends are named substitutively as ...polysulfanes (formerly: ...polysulfides). (230 pages)
Stewart, Charles D. (2006). Weapons of mass casualties and terrorism response handbook. Boston: Jones and Bartlett. p. 47. ISBN 0-7637-2425-4.

doi.org

Iijima, T.; Tsuchiy, S.; Kimura, M. (1977). "The Molecular Structure of Dimethyl Sulfide". Bull. Chem. Soc. Jpn. 50 (10): 2564. doi:10.1246/bcsj.50.2564.
Chauhan, Pankaj; Mahajan, Suruchi; Enders, Dieter (2014). "Organocatalytic Carbon–Sulfur Bond-Forming Reactions". Chemical Reviews. 114 (18): 8807–8864. doi:10.1021/cr500235v. PMID 25144663.
D. Landini; F. Rolla (1978). "Sulfide Synthesis In Preparation Of Dialkyl And Alkyl Aryl Sulfides: Neopentyl Phenyl Sulfide". Org. Synth. 58: 143. doi:10.15227/orgsyn.058.0143.
Hoyle, Charles E.; Bowman, Christopher N. (2010-02-22). "Thiol-Ene Click Chemistry". Angewandte Chemie International Edition. 49 (9): 1540–1573. doi:10.1002/anie.200903924. PMID 20166107.
Richter, Andreas M.; Engels, Volkmar; Beye, Norbert; Fanghänel, Egon (1989) [26 April 1989]. "Organische Elektronenleiter und Vorstufen IX: Zur Darstellung von Hexa-natrium-benzenhexathiolat aus Hexakis-benzylthio-benzen" [Organic electron-conductive materials and precursors IX: On synthesis of hexasodium benzenehexathiolate from hexakis(benzylthio)benzene]. Zeitschrift für Chemie (in German). 29 (12): 444. doi:10.1002/zfch.19890291206. Thioethergruppen können mit Alkali- bzw. Erdalkalimetallen in flüssigem Ammoniak oder in Aminen reduktiv entalkyliert werden. Orientierende Versuche ergaben, daß bei den Hexakisalkylthio-benzenen in flüssigem Ammoniak mit Natrium nicht nur die Alkyl-S-, sondern auch die Aryl-S-Bindung gebrochen wird. [Thioethers can be reductively dealkylated with alkali (resp. earth-alkali) metals in liquid ammonia or amines. Exploratory investigations revealed that not only the alkyl-S but also the aryl-S bonds cleave for hexakis(alkylthio)benzenes in liquid ammonia with sodium.]{{cite journal}}: CS1 maint: multiple names: authors list (link)

loc.gov

lccn.loc.gov

Brendsma & Arens 1967, p. 596. Brendsma, L.; Arens, J. F. (1967). "The chemistry of thioethers; differences and analogies with ethers". In Patai, Saul (ed.). The Chemistry of the Ether Linkage. The Chemistry of Functional Groups. London: Interscience / William Clowes and Sons. pp. 555–559. LCCN 66-30401.
Brendsma & Arens 1967, p. 601. Brendsma, L.; Arens, J. F. (1967). "The chemistry of thioethers; differences and analogies with ethers". In Patai, Saul (ed.). The Chemistry of the Ether Linkage. The Chemistry of Functional Groups. London: Interscience / William Clowes and Sons. pp. 555–559. LCCN 66-30401.
Brendsma & Arens 1967, p. 587. Brendsma, L.; Arens, J. F. (1967). "The chemistry of thioethers; differences and analogies with ethers". In Patai, Saul (ed.). The Chemistry of the Ether Linkage. The Chemistry of Functional Groups. London: Interscience / William Clowes and Sons. pp. 555–559. LCCN 66-30401.
Brendsma & Arens 1967, pp. 576–578. Brendsma, L.; Arens, J. F. (1967). "The chemistry of thioethers; differences and analogies with ethers". In Patai, Saul (ed.). The Chemistry of the Ether Linkage. The Chemistry of Functional Groups. London: Interscience / William Clowes and Sons. pp. 555–559. LCCN 66-30401.
Brendsma & Arens 1967, p. 581. Brendsma, L.; Arens, J. F. (1967). "The chemistry of thioethers; differences and analogies with ethers". In Patai, Saul (ed.). The Chemistry of the Ether Linkage. The Chemistry of Functional Groups. London: Interscience / William Clowes and Sons. pp. 555–559. LCCN 66-30401.
Brendsma & Arens 1967, pp. 555–559. Brendsma, L.; Arens, J. F. (1967). "The chemistry of thioethers; differences and analogies with ethers". In Patai, Saul (ed.). The Chemistry of the Ether Linkage. The Chemistry of Functional Groups. London: Interscience / William Clowes and Sons. pp. 555–559. LCCN 66-30401.

nih.gov

pubmed.ncbi.nlm.nih.gov

Chauhan, Pankaj; Mahajan, Suruchi; Enders, Dieter (2014). "Organocatalytic Carbon–Sulfur Bond-Forming Reactions". Chemical Reviews. 114 (18): 8807–8864. doi:10.1021/cr500235v. PMID 25144663.
Hoyle, Charles E.; Bowman, Christopher N. (2010-02-22). "Thiol-Ene Click Chemistry". Angewandte Chemie International Edition. 49 (9): 1540–1573. doi:10.1002/anie.200903924. PMID 20166107.