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Description
  • The reactions of selected triterpenic oxo compounds with Lawesson's reagent were investigated. We examined sulfurization of some oxygen compounds and for these reactions several hindered ketones, one aldehyde, α-hydroxyketones, esters, or anhydrides were chosen. We synthesized 15 new sulfur derivatives, including thioketone 16, dimeric sulfides 17-19, and thiaderivatives 20-22. We also observed unusual transformations, which afforded oxathiaphosphinines 23a, 23b, and dithiaphospholanes 24. The prepared compounds failed to demonstrate any significant cytotoxic activit
  • The reactions of selected triterpenic oxo compounds with Lawesson's reagent were investigated. We examined sulfurization of some oxygen compounds and for these reactions several hindered ketones, one aldehyde, α-hydroxyketones, esters, or anhydrides were chosen. We synthesized 15 new sulfur derivatives, including thioketone 16, dimeric sulfides 17-19, and thiaderivatives 20-22. We also observed unusual transformations, which afforded oxathiaphosphinines 23a, 23b, and dithiaphospholanes 24. The prepared compounds failed to demonstrate any significant cytotoxic activit (en)
Title
  • Reaction of lupane and oleanane triterpenoids with Lawesson's reagent
  • Reaction of lupane and oleanane triterpenoids with Lawesson's reagent (en)
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  • Reaction of lupane and oleanane triterpenoids with Lawesson's reagent
  • Reaction of lupane and oleanane triterpenoids with Lawesson's reagent (en)
skos:notation
  • RIV/00216208:11310/08:00011602!RIV12-GA0-11310___
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  • P(FT-TA/027), P(GA301/03/1570), P(GP203/05/P025), Z(AV0Z40550506), Z(MSM0021620857), Z(MSM6198959216)
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  • 17
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  • 391538
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  • RIV/00216208:11310/08:00011602
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  • Sulfur; Ketones; Lawesson's reagent; Terpenoids (en)
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  • US - Spojené státy americké
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  • [0C522C24F110]
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  • Tetrahedron
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  • 64
http://linked.open...iv/tvurceVysledku
  • Císařová, Ivana
  • Kvasnica, Miroslav
  • Šarek, Jan
  • Rudovská, Iva
http://linked.open...ain/vavai/riv/wos
  • 000254930400012
http://linked.open...n/vavai/riv/zamer
issn
  • 0040-4020
number of pages
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  • 10.1016/j.tet.2008.02.023
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  • 11310
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