From Wikipedia, the free encyclopedia
(Redirected from Thiadiazole)

In chemistry thiadiazoles are a sub-family of azole compounds, with the name thiadiazole originating from the Hantzsch–Widman nomenclature. Structurally, they are five-membered heterocyclic compounds containing one sulfur and two nitrogen atoms. They are aromatic ring by virtue of their two double bonds and the sulfur lone pair. Four possible structures exist depending on the relative positions of the heteroatoms; these forms do not interconvert and hence are structural isomers and not tautomers. The compounds themselves are rarely synthesized and possess no particular application, however, compounds bearing them as a structural motif are fairly common in pharmacology. 1,3,4-thiadiazole is the most common, appearing in such medications as cephazolin and acetazolamide. [1] [2] [3]

References

  1. ^ Hu, Yang; Li, Cui-Yun; Wang, Xiao-Ming; Yang, Yong-Hua; Zhu, Hai-Liang (2014). "1,3,4-Thiadiazole: Synthesis, Reactions, and Applications in Medicinal, Agricultural, and Materials Chemistry". Chemical Reviews. 114 (10): 5572–5610. doi: 10.1021/cr400131u. ISSN  0009-2665. PMID  24716666.
  2. ^ Jain, Abhishek Kumar; Sharma, Simant; Vaidya, Ankur; Ravichandran, Veerasamy; Agrawal, Ram Kishore (2013). "1,3,4-Thiadiazole and its Derivatives: A Review on Recent Progress in Biological Activities". Chemical Biology & Drug Design. 81 (5): 557–576. doi: 10.1111/cbdd.12125. ISSN  1747-0277. PMID  23452185. Open access icon
  3. ^ Wim Dehaen; Vasiliy A. Bakulev; Edward C. Taylor; Jonathan A. Ellman (27 April 2004). The Chemistry of Heterocyclic Compounds, The Chemistry of 1,2,3-Thiadiazoles. John Wiley & Sons. pp. 5–. ISBN  978-0-471-65691-3.
From Wikipedia, the free encyclopedia
(Redirected from Thiadiazole)

In chemistry thiadiazoles are a sub-family of azole compounds, with the name thiadiazole originating from the Hantzsch–Widman nomenclature. Structurally, they are five-membered heterocyclic compounds containing one sulfur and two nitrogen atoms. They are aromatic ring by virtue of their two double bonds and the sulfur lone pair. Four possible structures exist depending on the relative positions of the heteroatoms; these forms do not interconvert and hence are structural isomers and not tautomers. The compounds themselves are rarely synthesized and possess no particular application, however, compounds bearing them as a structural motif are fairly common in pharmacology. 1,3,4-thiadiazole is the most common, appearing in such medications as cephazolin and acetazolamide. [1] [2] [3]

References

  1. ^ Hu, Yang; Li, Cui-Yun; Wang, Xiao-Ming; Yang, Yong-Hua; Zhu, Hai-Liang (2014). "1,3,4-Thiadiazole: Synthesis, Reactions, and Applications in Medicinal, Agricultural, and Materials Chemistry". Chemical Reviews. 114 (10): 5572–5610. doi: 10.1021/cr400131u. ISSN  0009-2665. PMID  24716666.
  2. ^ Jain, Abhishek Kumar; Sharma, Simant; Vaidya, Ankur; Ravichandran, Veerasamy; Agrawal, Ram Kishore (2013). "1,3,4-Thiadiazole and its Derivatives: A Review on Recent Progress in Biological Activities". Chemical Biology & Drug Design. 81 (5): 557–576. doi: 10.1111/cbdd.12125. ISSN  1747-0277. PMID  23452185. Open access icon
  3. ^ Wim Dehaen; Vasiliy A. Bakulev; Edward C. Taylor; Jonathan A. Ellman (27 April 2004). The Chemistry of Heterocyclic Compounds, The Chemistry of 1,2,3-Thiadiazoles. John Wiley & Sons. pp. 5–. ISBN  978-0-471-65691-3.

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