PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
26435899-7	2015	We demonstrate an efficient procedure for the preparation of anti and syn beta(2,3)-amino acids with alkyl side chains, from alpha-amino acids in reasonable yields.	Amino Acids	125-142	synemin	Homo sapiens	70-73	
25867051-2	2015	The method utilizes simple alpha-amino acids to deliver syn- and anti- selective isoindolinones with remarkably high enantioselectivity (up to >99% ee) in good to excellent yields and diastereomeric ratios.	Amino Acids	27-44	synemin	Homo sapiens	56-59	
11856002-3	2002	Oxidation of the metal carbene moiety followed by basic hydrolysis of the esters afforded enantiomerically highly enriched syn,exo-3,4,5-trisubstituted prolines, whereas acidic hydrolysis of the same functional groups proceeded with epimerization at the alpha-amino acid center leading to anti,exo-3,4,5-trisubstituted prolines of very high enantiomeric purity as well.	Amino Acids	254-270	synemin	Homo sapiens	123-126	
28763205-3	2017	Subsequent in situ enantioselective [2,3]-sigmatropic rearrangement catalyzed by the isothiourea benzotetramisole forms syn-alpha-amino acid derivatives with high diastereo- and enantioselectivity.	Amino Acids	124-140	synemin	Homo sapiens	120-123