PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
18688343-1	2008	Benzylic zinc reagents prepared by direct insertion of zinc to benzylic chlorides in the presence of LiCl undergo smooth cross-coupling reactions with aromatic chlorides, bromides and tosylates using Ni(acac)(2) and PPh(3) as a catalyst system.	Bromides	171-179	caveolin 1	Homo sapiens	216-222	
18604829-3	2008	In particular, the cross-coupling reactions of the benzylic zinc chlorides with aromatic chlorides, bromides, and tosylates in the presence of [Ni(acac)(2)] (acac=acetylacetonate) and PPh(3) proceeded in good to excellent yields to give the corresponding diaryl and heterodiaryl methanes.	Bromides	100-108	caveolin 1	Homo sapiens	184-190	
10836067-2	1999	A more general Pd(0)-catalyst/ligand system has been developed to activate bromides: palladium(II) acetate (Pd(OAc)2) is activated with triphenylphosphine (PPh3) or tri-o-tolylphosphine (P(o-tol)3) (1:2 molar ratio of Pd:phosphine).	Bromides	75-83	caveolin 1	Homo sapiens	156-160	
31904056-0	2020	Hydride, chloride, and bromide show similar electronic effects in the Au9(PPh3)83+ nanocluster.	Bromides	23-30	caveolin 1	Homo sapiens	74-78	
31904056-2	2020	We present electronic absorption spectra of precisely mass-selected Au9(PPh3)83+ clusters featuring a surface hydride, chloride, or bromide.	Bromides	132-139	caveolin 1	Homo sapiens	72-76