Rujukan Sulfida (organik)

  1. ↑ Cremlyn, R. J. (1996). An Introduction to Organosulfur Chemistry. Chichester: John Wiley and Sons. ISBN 0-471-95512-4.
  2. ↑ 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.
  3. ↑ Chauhan, Pankaj; Mahajan, Suruchi; Enders, Dieter (2014). "Organocatalytic Carbon–Sulfur Bond-Forming Reactions". Chemical Reviews. 114 (18): 8807–8864. doi:10.1021/cr500235v.
  4. ↑ D. Landini And 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.
  5. ↑ Hoyle, Charles E.; Bowman, Christopher N. (22 February 2010). "Thiol-Ene Click Chemistry". Angewandte Chemie International Edition. 49 (9): 1540–1573. doi:10.1002/anie.200903924. PMID 20166107.
  6. ↑ Stewart, Charles D. (2006). Weapons of mass casualties and terrorism response handbook. Boston: Jones and Bartlett. m/s. 47. ISBN 0-7637-2425-4.
  7. Hellwinkel, Dieter (2012-12-06). Systematic Nomenclature of Organic Chemistry: A Directory to Comprehension and Application of its Basic Principles (ed. 1). Springer Science & Business Media. m/s. 131. ISBN 978-3-64256765-0. m/s. 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)