PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
30443158-2	2004	An ester-derived titanium enolate mediated syn-aldol reaction was employed to generate the stereocenters C-5 and C-6.	Esters	3-8	complement C6	Homo sapiens	113-116	
25736157-3	2015	The reaction occurs most likely through an initial intramolecular amino-amide interaction, followed by an N- to O-acyl transfer of the side chain from C-4 to the C-6 position to form an ester intermediate (5), detectable by NMR, and subsequent hydrolysis.	Esters	186-191	complement C6	Homo sapiens	162-165	
12128171-2	2002	The esters synthesized (1 and 2) link AZT, by a succinyl linker, to the C-3 position of glucose and to C-6 of galactose.	Esters	4-10	complement C6	Homo sapiens	103-106	
9680411-2	1998	Glycosylation of the derived acceptor with reactive groups only at C-6 with an ortho ester of d-mannose proceeded smoothly in dichloromethane in the presence of trimethylsilyl trifluoromethanesulfonate, and the degree of branching was up to 0.6.	Esters	85-90	complement C6	Homo sapiens	67-70	
15760187-3	2005	Indolizine 6, containing an ester group at C-6, was reductively alkylated to give dihydroindolizines 8 and 9 possessing a quaternary carbon center in good yield.	Esters	28-33	complement C6	Homo sapiens	43-46	
24076198-5	2013	The conjugation of GA onto chitosan probably occurred between amine (C-2), hydroxyl groups (C-3 and C-6) of chitosan and carboxyl groups of GA, forming amide and ester linkages, respectively.	Esters	162-167	complement C6	Homo sapiens	100-103	
22530559-1	2012	Chiral 2-piperidinone compounds with various C-6 substituents were successfully synthesized via a Pd-catalyzed asymmetric 6-endo cyclization of dienamides, which were evidently activated by both N-p-toluenesulfonyl and C-3 ester substituents.	Esters	223-228	complement C6	Homo sapiens	45-48	
22229781-3	2012	Even more remarkably, in contrast with the C-6 regioselectivity of other reactions of cellulose and its derivatives, this deacylation shows substantial selectivity for the removal of the acyl groups from the esters of the secondary alcohols at C-2 and C-3, affording cellulose-6-O-esters with high regioselectivity by a simple one-step process employing no protective groups.	Esters	208-214	complement C6	Homo sapiens	43-46