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Bis tetrahydrofuran

Scheme 8.2 Kishi s method for the construction of the bis(tetrahydrofuran) core of isolasalocid A. Scheme 8.2 Kishi s method for the construction of the bis(tetrahydrofuran) core of isolasalocid A.
These changes are more consistent with an /-effect, rather than an R-effect, on the B—C bond. That such diborylacetylenes have a diminished electron density at boron relative to alkyl- and vinylboranes is evident from their enhanced Lewis acidity bis(diethylboryl)acetylene (40) forms a bis(tetrahydrofuran) complex, as is evident from the1 B NMR spectrum37 (Eq. 11). Alkyl- and vinylboranes exhibit no such shifts in their11B signals in THF solution. [Pg.366]

The reductive coupling of guaiazulene, a fulvalene analog, with activated calcium in THF affords a 60 40 mixture of two isomers, 8,8 -147 (Figure 75) and 8,6 -(diguaiazulenide)bis(tetrahydrofuran)calcium, respectively. Thermolyses of each isomer revealed that the 8,8 -isomer is the thermodynamically preferred isomer, and it forms preferentially when the coupling is performed at 67 °C.342... [Pg.129]

The analogous triphenylzincate 60 and trimesitylzincate 61 were obtained by the treatment of zinc bromide bis(tetrahydrofuranate) with the respective Grignard reagents, as outlined in Scheme 48.1... [Pg.345]

More complex molecules can also be synthesized employing the Williamson procedure. Thus, on treatment with NaH, the mesylate 86 provides the tetrahydrofuran in excellent yield and stereo-control . In a similar manner, tosylate 87 undergoes the same reaction to lead to the bis-tetrahydrofuran <00EJO1889>. [Pg.148]

Stereoselective intramolecular oxymercuration of carbohydrate derivatives was proposed as the key reaction for efficient preparation of mono- and dihydroxylated unsymmetrical bis-tetrahydrofuran skeletons present in naturally occurring biologically active acetogenins. The trans- and. mz-selective intramolecular oxymercurations were explored in an enantioselective synthesis of the bis-tetrahydrofuran skeleton of mucoxin (Fig. 57).73... [Pg.250]

The explosive carbonylalkali-metals , previously formulated as monomeric compounds, are either dimeric acetylene derivatives of the general formula MOC=COM. or are trimers of the latter and formulated as salts of hexahydroxybenzene. Many true carbonylmetal complexes are air-sensitive and pyrophoric, not always immediately. Individually indexed compounds are Bis(dicarbonylcyclopentadienyliron)-bis(tetrahydrofuran)magnesium, 3835... [Pg.80]

Bis(cyclopentadienyl)phenylvanadium, 3705 Bis(cyclopentadienyl)titanimn, 3295 Bis(cyclopentadienyl)titanium selenate, 3293 Bis(cyclopentadienyl)zirconium, 3296 Bis(dicarbonylcyclopentadienyliron)-bis(tetrahydrofuran)magnesium, 3835... [Pg.303]

Bis(tetrahydrofurane)(meso-tetraphenylporphinato)iron(II) (bTHF FeTPP) is the only known six-coordinate high-spin Fe(II) complex. Its THF ligands are rather loosely bound. Crystals slowly lose THF when exposed to the atmosphere, while the iron is five-coordinate in a solution in benzene (Reed et al. 1980). The magnetic susceptibilty of bTHF FeTPP is temperature dependent (Lecomte et al. 1986) and the axial Fe—O bonds shrink on cooling from 1.35 A at ambient temperature to 1.29 A at nitrogen temperature. [Pg.231]

Nitrile lassen sich mittels Niobium(IV)-chlorid-Bis-tetrahydrofuran/Tributylstannan in Thiolan reduktiv zu vicinalen Diaminen kuppeln1. Die Ausbeuten sind dabei im allge-meinen etwas geringer als bei der vorgenannten, von N-Silyl-iminen ausgehenden Me-thode. [Pg.1129]

F. BIS(TETRAHYDROFURAN)-l,2-BIS(2-HYDROXY-3,5-BIS (fcrf-BUTYL)BENZYLIDENEIMINO)ETHANEALUMINUM TETRAPHENYLBORATE, [Al( BuSalen)(THF)2][BPh4]... [Pg.19]

TRIS(TRIMETHYLSILYL)SILYL LITHIUM TRIS(TETRAHYDROFURAN), LITHIUM TRIS(TRIMETHYLSILYL)SILYLTELLUROLATE BIS(TETRAHYDROFURAN), AND TRIS(TRIMETHYLSILYL)SILYLTELLUROL ... [Pg.162]

The systematic names for these compounds are lithium 1,1,1,3,3,3-hexamethyl-2-(trimethyl-silyl)-2-trisilanetellurolate-bis(tetrahydrofuran) and 1,1,1,3,3,3-hexamethyl-2-(trimethylsilyl)-2-trisilanetellurol. [Pg.162]

Lithium tris(trimethylsilyl)silyltellurolate bis(tetrahydrofuran) is a pale yellow, air-sensitive solid that is soluble in hydrocarbons, diethyl ether, and THF. The finely powdered solid oxidizes (sometimes pyrophorically) in air to give the dark green ditelluride (SiMe3)3SiTeTeSi(SiMe3)3.8 The lithium tellu-rolate is dimeric in the solid state as shown by X-ray crystallography10... [Pg.164]

Li02Si4TeC)7H43, Lithium, [l,l,l,3,3,3-hexamethyl-2-(trimethylsilyl)-2-trisilanetellurolato]bis(tetrahydrofuran)-, [152758-18-4], 31 164... [Pg.330]


See other pages where Bis tetrahydrofuran is mentioned: [Pg.283]    [Pg.305]    [Pg.305]    [Pg.490]    [Pg.12]    [Pg.1278]    [Pg.1015]    [Pg.190]    [Pg.894]    [Pg.150]    [Pg.516]    [Pg.250]    [Pg.218]    [Pg.245]    [Pg.245]    [Pg.230]    [Pg.233]    [Pg.234]    [Pg.152]    [Pg.1129]    [Pg.1130]    [Pg.421]    [Pg.8]    [Pg.9]    [Pg.164]    [Pg.325]   


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Benzene, o-bis tetrahydrofuran complex

Benzene, o-bis tetrahydrofuran complex crystal structure

Bis[tetrahydrofuran-2-ylmethyl

Copolymerization of Tetrahydrofuran with 3,3-Bis(chloromethyl) Oxetane

Tris(trimethylsilyl)silyltellurolate Bis(tetrahydrofuran)

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