Stannane /ˈstæneɪn/ or tin hydride is an inorganic compound with the chemical formula SnH4. It is a colourless gas and the tin analogue of methane. Stannane...
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Organotin chemistry (redirect from Stannanes)
scientific study of the synthesis and properties of organotin compounds or stannanes, which are organometallic compounds containing tin–carbon bonds. The first...
24 KB (2,623 words) - 18:21, 19 September 2024
Stille reaction (section Stannane)
is widespread. In regards to limitations, both very bulky stannane reagents and stannanes with substitution on the α-carbon tend to react sluggishly...
47 KB (5,491 words) - 13:23, 22 February 2024
Fentin acetate (redirect from Stannane, acetoxytriphenyl-)
Fentin acetate Names IUPAC name (acetoxy)(triphenyl)stannane Other names Phentin acetate; Triphenyltin acetate; Triphenylstannyl acetate; Acetic acid tri(phenyl)stannyl...
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Organostannane addition (redirect from Allylic stannane addition)
number of acyclic transition states. (E)-Stannanes exhibit higher syn selectivity than the corresponding (Z)-stannanes. (3) In the presence of certain Lewis...
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Related alkanes Ethane Propane Butane Related compounds Silane Germane Stannane Plumbane Supplementary data page Methane (data page) Except where otherwise...
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alkynes, and all hydrocarbons silicon: silane germanium: germane tin: stannane lead: plumbane nitrogen: ammonia ("azane" when substituted), hydrazine...
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fluoroacetate Sodium pentachlorophenate Sodium selenate Sodium selenite Stannane, acetoxytriphenyl- Strychnine Strychnine sulfate Sulfotep Sulfoxide, 3-chloropropyl...
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germane GeH4 and digermane Ge2H6. They are germanium analogues of alkanes. Stannane SnH4, a strong reducing agent slowly decomposes at room temperature to...
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+4 oxidation states: tin(II) sulfide and tin(IV) sulfide (mosaic gold). Stannane (SnH 4), with tin in the +4 oxidation state, is unstable. Organotin hydrides...
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replaced by an aryl boronic acid and in the Stille reaction by an aryl stannane. The cycle also extends to the other group 10 element nickel for example...
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alkynes. The typical stannane is tributyltin hydride. The reaction mechanism is assumed to operate via oxidative addition of the stannane to give a stannyl...
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is unstable as compared to its lighter congeners silane, germane, and stannane. It cannot be made by methods used to synthesize GeH4 or SnH4. In 1999...
8 KB (723 words) - 09:44, 9 April 2024
−136 52 75-10-5 Difluorocarbamyl fluoride F2NCOF −52 −152.2 99 2368-32-3 Stannane SnH4 −51.8 −146 123 2406-52-2 Tetrafluoropropyne CF3C≡CF −50.39 112 20174-11-2...
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stable primary alkoxy stannane in solution. The reaction is then quenched irreversibly, with the less hindered primary alkoxy stannane reacting more rapidly...
29 KB (3,757 words) - 15:11, 13 February 2024
Retrieved 2021-04-21. TETRAVINYLTIN - ChemicalBook Tetravinylstannane at Encyclopedia of Reagents for Organic Synthesis Stannane, tetraethenyl at NIST WebBook...
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This biosynthesis can be mimicked in the laboratory by preparing allylic stannane from farnesol, termed Corey synthesis. There are diverse ways to synthesize...
16 KB (1,706 words) - 21:56, 3 September 2023
0564 Related compounds Related tetrahydride compounds Methane Germane Stannane Plumbane Related compounds Phenylsilane Vinylsilane Disilane Trisilane...
20 KB (2,208 words) - 16:40, 22 September 2024