PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
29323365-3	2018	In contrast, reaction of 1a with [Ir2Cl2(COD)2] (COD = 1,5-cyclo-octadiene) affords the complex [IrCl(COD){kappa2-P,P"-H2C(NCH2PPh2)2C10H6}], thermolysis of which affords cyclo-octene and the pincer-NHC complex [IrCl{kappa3-C,P,P"-C(NCH2PPh2)2C10H6}].	1,5-cyclooctadiene	55-74	COD2	Homo sapiens	41-46	
29441396-2	2018	Reaction of (PPh2)2BMes with Ni(COD)2 or Pt(COD)Me2 (COD = 1,5-cyclooctadiene) results in gradual COD displacement to give [eta3-P,B,P-(PPh2)2BMes]Ni(COD) (3) or [eta3-P,B,P-(PPh2)2BMes]Pt(CH3)2 (6).	1,5-cyclooctadiene	59-77	COD2	Homo sapiens	32-37	
29116776-3	2017	We report detailed mechanistic analysis of the hydrogenolysis of diaryl ethers catalyzed by the combination of Ni(COD)2 (COD = 1,5-cyclooctadiene) and an N-heterocyclic carbene (NHC).	1,5-cyclooctadiene	127-145	COD2	Homo sapiens	111-119	
29149562-1	2017	In the presence of a catalytic amount of Ni(cod)2 (cod = 1,5-cyclooctadiene) and PCy3 (Cy = cyclohexyl), the cross-tetramerization of tetrafluoroethylene (TFE), alkynes, and ethylene occurred in a highly selective manner to afford a variety of 1,3-dienes with a 3,3,4,4-tetrafluorobutyl chain.	1,5-cyclooctadiene	57-75	COD2	Homo sapiens	41-49	
26226412-5	2015	These complexes were synthesized in higher yields from the reaction of with Ni(COD)2, where COD = 1,5-cyclooctadiene.	1,5-cyclooctadiene	98-116	COD2	Homo sapiens	79-84	
27629250-1	2016	Various aryl-, alkenyl-, and/or alkyllithium species reacted smoothly with aryl and/or benzyl ethers with cleavage of the inert C-O bond to afford cross-coupled products, catalyzed by commercially available [Ni(cod)2 ] (cod=1,5-cyclooctadiene) catalysts with N-heterocyclic carbene (NHC) ligands.	1,5-cyclooctadiene	224-242	COD2	Homo sapiens	211-216	
26952589-2	2016	Treatment of the homoleptic, 8-coordinate M(NP)4 monometallic precursors with Ni(COD)2 (COD = 1,5-cyclooctadiene) yielded the heterobimetallic complexes (kappa(2)-NP)M(mu2-NP)3Ni (M = Ti, Zr, Hf).	1,5-cyclooctadiene	94-112	COD2	Homo sapiens	81-86	
25693968-2	2015	Reported herein is that 1,4-dilithio-1,3-butadienes reacted with [Ni(cod)2] (cod = 1,5-cyclooctadiene) to deliver dilithionickeloles.	1,5-cyclooctadiene	83-101	COD2	Homo sapiens	69-74	
24526274-4	2014	In these media, spontaneous decomposition of Ni(COD)2 (COD = 1,5-cyclooctadiene) in the absence of H2 occurred giving small NPs (<=4 nm) with narrow size distributions.	1,5-cyclooctadiene	61-79	COD2	Homo sapiens	45-53	
17441112-1	2006	In the 1,4-addition of phenylboronic acid to alpha,beta-unsaturated ketones, [Rh(OH)(cod)]2 has a much higher catalytic activity than [Rh(OH)(binap)]2 (cod = 1,5-cyclooctadiene, binap = 2,2"-bis(diphenylphosphanyl)-1,1"-binaphthyl).	1,5-cyclooctadiene	158-176	COD2	Homo sapiens	85-91	
30521318-1	2018	In the presence of a catalytic amount of Ni(cod)2 (cod = 1,5-cyclooctadiene) and PCy3 (Cy = cyclohexyl), the cross-tetramerization of tetrafluoroethylene (TFE), ethylene, alkynes, and aldehydes leads to a variety of fluorine-containing enone derivatives.	1,5-cyclooctadiene	57-75	COD2	Homo sapiens	41-49	
34180473-2	2021	In the case of Ni(COD)2 (COD = 1,5-cyclooctadiene), a dianionic sandwich-like cluster (Ni{Ge9(Hyp)3}2)2- (1) was obtained, in line with a simple ligand substitution reaction of COD by (Ge9(Hyp)3)-.	1,5-cyclooctadiene	31-49	COD2	Homo sapiens	15-23	
31576866-1	2019	The reaction of the phosphine functionalized chlorogermylene 1 with Ni(COD)2 (COD = 1,5-cyclooctadiene) afforded the bis-chlorogermylene ligated nickel(0) complex 2 in high yield.	1,5-cyclooctadiene	86-102	COD2	Homo sapiens	71-76	
30816389-3	2019	When reduction is performed in the presence of 1,5-cyclooctadiene (COD), [Ni(COD)2] is obtained.	1,5-cyclooctadiene	47-65	COD2	Homo sapiens	77-82	
30500210-6	2019	When 3 was allowed to react with Ni(cod)2 (cod = 1,5-cyclooctadiene), the unique {[SiII(Xant)SiII]GeI}2NiII complex with a three-membered ring Ge2Ni-metallacycle was obtained via reductive coupling of two Ge0 atoms on the Ni center.	1,5-cyclooctadiene	49-67	COD2	Homo sapiens	33-41