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2OH) in 87% yield using tetrakistriphenylphosphinepalladium(0), but prepared 1,2-diethynylbenzene using the bistrimethylsilyl derivative.
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85035169908
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See e.g. Catalogue for 1995-6 Aldrich Chemical Company
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See e.g. Catalogue for 1995-6 Aldrich Chemical Company.
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17
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85035167166
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note
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We observed rapid volatilisation of 1,4-diethynylbenzene on the rotary evaporator at ca. 45°C bath temperature. Ref. 11 reports deprotection of this compound using toluene with quantitative recovery, but without details of the evaporation conditions.
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18
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19
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85035165010
-
-
Reactions of the alkynes described in this paper with decaborane derivatives will be described elsewhere
-
Reactions of the alkynes described in this paper with decaborane derivatives will be described elsewhere.
-
-
-
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20
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33845379479
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21
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85035169791
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note
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3 per mmole of catalyst) under dinitrogen at ca. 60°C.
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23
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84861168413
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