PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 18931770-1 2008 The three-component coupling of benzynes with terminal alkynes and activated alkenes in the presence of CuI, PCy(3) and CsF in a 1:1 mixture of CH(3)CN and THF at 50 degrees C for 5 h gave 1-alkyl-2-alkynylbenzenes in good to moderate yields. tetrahydrofuran 156-159 colony stimulating factor 2 Homo sapiens 120-123 18399650-1 2008 Treatment of 1-bromo-2,2-dichloro-3-trimethylsilylcyclopropane with CsF in THF refluxing temperature gave chlorocyclopropenyl cation (1), which reacted with various nucleophiles to generate 3-monosubstituted 1-chlorocyclopropenes. tetrahydrofuran 75-78 colony stimulating factor 2 Homo sapiens 68-71 11327904-6 2001 Reaction of 2 with the disiloxane (CF(2)CH(2)OSiMe(3))(2), in the presence of catalytic amounts of CsF in THF at 90 degrees C, resulted in the formation of the dispiro compound [(CF(2)CH(2)O)(2)PN](2)[4-t-BuC(6)H(4)(O)SN] (4). tetrahydrofuran 106-109 colony stimulating factor 2 Homo sapiens 99-102 11304158-5 2001 In the presence of catalytic amounts of CsF in THF, the bridged compound 3 was converted to the spirocyclic compound 2 while the 1,3-ansa compound 6 under similar conditions transformed into the monospiro-substituted compound CH2(CH2O)2 (PN)(F2PN)3 (7). tetrahydrofuran 47-50 colony stimulating factor 2 Homo sapiens 40-43 11198851-4 2000 The ansa isomers 3a and 3b are transformed into the spiro compound 6 in the presence of catalytic amounts of CsF at room temperature in THF, while 4a and 4b are transformed into the spiro compound [PhCH2P(S)(CH2O)2PN](F2PN)2 (7) under similar conditions. tetrahydrofuran 136-139 colony stimulating factor 2 Homo sapiens 109-112 18963717-1 1984 The solubilities of LiF, NaF, KF, RbF and CsF in acetonitrile, acetone, tetrahydrofuran, dimethylformamide, benzene and cyclohexane have been determined with and without a crown ether (usually 0.1 M 18-crown-6) present. tetrahydrofuran 72-87 colony stimulating factor 2 Homo sapiens 42-45