PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
16149811-1	2005	[reactions: see text] The glycosylation with trichloroacetimidates derived from different glycopyranoses bearing a nonparticipating group at C-2 was explored in different ionic liquids as solvents.	trichloroacetamide	45-66	complement C2	Homo sapiens	141-144	
31830633-4	2020	On the other hand beta-stereoselectivity of rhamnosyl trichloroacetimidate donors protected with O-picoloyl groups at remote positions (C-2 and C-3) has been investigated while the glycosylation reactions of 2-O-picoloyl group substituted l-rhamnosyl donor displays predominant beta-stereoselectivity.	trichloroacetamide	44-74	complement C2	Homo sapiens	136-147	
16122263-5	2005	Here, we report the gram-scale syntheses of both types of epitopes by an approach that utilizes glucosyl trichloroacetimidate donor 2 to first create a beta-glucopyranoside linkage and then epimerizes the C-2 center via an oxidation-reduction sequence that provides an efficient multigram scale route to the beta-mannopyranosides 5, 8, and 15.	trichloroacetamide	105-125	complement C2	Homo sapiens	205-208	
12204620-4	2002	The alpha-(1-->3)-linkage was formed in considerable amount with galactose mono- and disaccharide trichloroacetimidate donors with C-2 neighboring group participation.	trichloroacetamide	101-121	complement C2	Homo sapiens	134-137