PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
12837097-2	2003	The 1-oxide 1a also reacted even with angle-strained dienophiles acenaphthylene and norbornene at its syn-pi-face to afford [4+2] adducts; in the latter case, norbornene reacted exclusively at its exo-pi-face.	2-norbornene	84-94	synemin	Homo sapiens	102-105	
12837097-2	2003	The 1-oxide 1a also reacted even with angle-strained dienophiles acenaphthylene and norbornene at its syn-pi-face to afford [4+2] adducts; in the latter case, norbornene reacted exclusively at its exo-pi-face.	2-norbornene	159-169	synemin	Homo sapiens	102-105	
12444634-9	2002	Our theoretical data correctly reproduce the experimental facial syn selectivity of norbornene and norbornadiene epoxidations and compare well with the experimental activation free energies of the peroxy acid epoxidation of all the olefins reported here.	2-norbornene	84-94	synemin	Homo sapiens	65-68