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Triethyl germane

The THF-containing complexes formed between trinitrobenzene and the lithium or potassium salts of trimethyl-, triethyl- or triphenyl-germanate, -silanate or -stannate decompose explosively on heating, though trinitrobenzene-potassium trimethyl-stannate decomposes explosively at ambient temperature. [Pg.686]

This route is named after our hero, the brilliant German chemist, Karl Ziegler. He found that triethyl aluminum could, under the right conditions, be used as a kind of seed for growing hydrocarbon chains. These chains can be manipulated to yield either straight-chain primary olefins or, in the application for this chapter, linear, straight-chain primary alcohols. (The olefins, referred to as alpha olefins because the double bond occurs in next to the last carbon, are covered in Chapter 21, Alpha Olefins.)... [Pg.217]

Treatment of a solution of bromotrilluoromethane and chloiotriethylgcrmane in dichloro-methane with tris(dicthylamino)phosphane at — 60 C and heating the mixture to 20-22 C leads to formation of triethyl(trifluoromclhyl)germane (52-66% bp 147 C) and the corresponding phosphonium salt. ... [Pg.405]

TRI-(l-AZIRIDINYL)-p-BENZOQUINONE 2,3,5-TRIETHYLE.NEIM1NO-1,4-BENZOQUINONE TRIETHYLENIMINOBENZOQUINONE TRISAETHYL-ENBVDNOBENZOCHINON (GERMAN) 2,3,5-TRIS-(AZIRIDINO)-l,4-BENZOQUINONE 2,3,5-TRIS(l-AZIRIDINO)-p-BENZOQUINONE TRIS(AZIRIDINYL)-p-BENZOQUINONE 2,3,5-TRIS(l-AZIRIDINYL)-p-BENZOQUINONE 2,3,5-TRIS(AZIRIDINYL)-l,4-... [Pg.1399]

SYNS APHOXIDE APO 1-AZIRIDINYL PHOSPHINE OXIDE (TRIS) (DOT) CBC 906288 ENT 24,915 IMPERON FIXER T NSC 9717 l,l, l"-PHOSPHINYL-IDYNETRISAZIRIDINE PHOSPHORIC ACID TRIETHYLENE IMIDE PHOSPHORIC ACID TRIETHYL-ENEIMINE (DOT) SK-3818 TEF TEPA TRIA-ETHYLENPHOSPHORSAEUREAMID (GERMAN) TRIAZIRIDINOPHOSPHINE OXIDE TRI(AZIRIDIN-YL)PHOSPHINE OXIDE TRI(-l-AZIRIDINYL)PHOSPH-INE OXIDE NN A" -TRI-1>ETHANEDIYL PHOSPHORIC TRIMIDE TRIETHYLENEPHOS-PHOROTRIAMIDE TRIS(1-AZIRIDINE)PHOSPHINE OXIDE TRIS(N-ETHYLENE)PHOSPHOROTRI. MID-ATE... [Pg.1399]

Dicyclohexyl percarbonate converted bis[triethylgermyl] tellurium to triethyl(cyclohex-yloxy)germane. ... [Pg.20]

A comparative study of the chelation of 2-deoxy-D-ribose with boric, germanic, telluric, and arsenious acids using potentiometry has shown that only 1 1 complexes are formed. Values of the chelation constants were compared with those of the pentoses. A similar study on mannitol and glucose with boric acid demonstrated that the former was about 740 times more effective a complexant than glucose, but that the conclusions were complicated by the degree of association of boric acid in solution. Reactions at the anomeric centre of mannofuranose have been carried out by means of the 2,3 5,6-ethylboronate (1) formed by treatment of D-mannose with limited triethyl boroxine. By the same means D-lyxose gave the 2,3-blocked lyxofuranose (2) also useful for... [Pg.138]

Triethyl(benzylthio)germane. Benzyl(triethylgermyl)-suljide. Triethyl(phenylmethyl)germane... [Pg.26]

See other pages where Triethyl germane is mentioned: [Pg.107]    [Pg.769]    [Pg.408]    [Pg.467]    [Pg.33]    [Pg.445]    [Pg.31]    [Pg.300]    [Pg.107]    [Pg.769]    [Pg.408]    [Pg.467]    [Pg.33]    [Pg.445]    [Pg.31]    [Pg.300]    [Pg.19]    [Pg.304]    [Pg.23]    [Pg.25]    [Pg.33]    [Pg.15]    [Pg.23]    [Pg.25]    [Pg.33]    [Pg.424]    [Pg.831]    [Pg.1391]    [Pg.428]    [Pg.307]    [Pg.405]    [Pg.428]    [Pg.43]    [Pg.1127]    [Pg.169]    [Pg.21]    [Pg.27]   
See also in sourсe #XX -- [ Pg.467 ]



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2.4.5- Triethyl

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