Thiourea, A convenient reagent for the reductive cleavage of olefin ozonolysis products☆
References (29)
- et al.
Org. Synthesis
(1961) - et al.
Synthesis
(1974) - et al.
Perfumer and Flavorist
(1979) Chem. Rev.
(1958)- et al.
J. Am. Chem. Soc.
(1943) - et al.
J. Am. Chem. Soc.
(1952) - et al.
J. Org. Chem.
(1961)
J. Org. Chem.
(1960)
J. Org. Chem.
(1968)
et al.Helv. Chim. Acta
(1967)
Tetrahedron Letters
(1966)
Cited by (57)
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2022, Journal of Molecular LiquidsCitation Excerpt :Also, thiourea is used for vulcanization accelerator, auxiliary agent for all types of copy paper, silver gelatin photographic print and solution in Sn (II) for copper printed. Among its chemical reactions are kurnakov reaction, silver polishing, a precursor to heterocycles, source of sulphide and reluctant[177–180]. Its most important uses are used as a precursor in the preparation of the heterocyclic compound.
Alkene ozonolysis
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Antibiotic long-chain and α,β-unsaturated aldehydes from the culture of the marine fungus Cladosporium sp.
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MRC Communication No. 34.
Copyright © 1982 Published by Elsevier Ltd.