PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
3445286-0	1986	Stereoselective reduction of C-2 substituted steroid C-3 ketones with lithium tris-(R,S-1,2-dimethylpropyl)-borohydride and sodium borohydride.	Ketones	57-64	complement C2	Homo sapiens	29-32	
1499340-2	1992	Thiamin pyrophosphate catalyzes various decarboxylation and transfer reactions involving ketone groups because the thiazolium ring with its positively charged N atom can, on the loss of a proton from the adjacent C-2, generate a ylid which adds to carbonyl groups to produce a substrate ylid.	Ketones	89-95	complement C2	Homo sapiens	213-216	
31823472-0	2020	C-1 Oxidation/C-2 Reduction Isomerization of Unprotected Aldoses Induced by Light/Ketone.	Ketones	82-88	complement C2	Homo sapiens	14-17	
19582307-2	2009	The reductive hydroxyalkylation of nitrone 10 with ketones and aromatic aldehydes is highly diastereoselective in establishing the C-2 chiral center of the pyrrolidine ring.	Ketones	51-58	complement C2	Homo sapiens	131-134	
27736082-0	2016	Electronic Nature of Ketone Directing Group as a Key To Control C-2 vs C-4 Alkenylation of Indoles.	Ketones	21-27	complement C2	Homo sapiens	64-67	
27736082-1	2016	A novel mode of achieving site selectivity between C-2 and C-4 positions in the indole framework by altering the property of the ketone directing group is disclosed.	Ketones	129-135	complement C2	Homo sapiens	51-54	
25493619-1	2014	Bis(isonitrile) iron(II) complexes bearing a C2-symmetric N2P2 macrocyclic ligand, which are easily prepared from the corresponding bis(acetonitrile) analogue, catalyze the asymmetric transfer hydrogenation (ATH) of a broad scope of ketones in excellent yields (up to 98%) and with high enantioselectivity (up to 91% ee).	Ketones	233-240	complement C2	Homo sapiens	45-81	
15476708-2	2004	Whereas C-2- and 4-ulopyranosyl compounds (C-2- and C-4-ulosides) can be converted to cyclopentenones under base conditions through beta-elimination and ring contraction, base-initiated beta-elimination of C-glycosyl 2"-aldehydes and 2"-ketones results in the formation of acyclic alpha,beta-unsaturated aldehydes or ketones.	Ketones	237-244	complement C2	Homo sapiens	8-18	
15476708-2	2004	Whereas C-2- and 4-ulopyranosyl compounds (C-2- and C-4-ulosides) can be converted to cyclopentenones under base conditions through beta-elimination and ring contraction, base-initiated beta-elimination of C-glycosyl 2"-aldehydes and 2"-ketones results in the formation of acyclic alpha,beta-unsaturated aldehydes or ketones.	Ketones	237-244	complement C2	Homo sapiens	8-11