PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
21359299-2	2011	These new primary-tertiary diamine-Bronsted acid conjugates bifunctional organocatalysts efficiently catalyzes the asymmetric direct syn selective cross-aldol reaction of different protected hydroxyacetone with various aldehydes in high yield (94%) and high enantioselectivity (up to 97% ee of syn) and dr of 91 : 9 (syn/anti) under mild reaction conditions.	diamine-bronsted acid	27-48	synemin	Homo sapiens	133-136
18215050-1	2008	We present herein simple primary-tertiary diamine-Bronsted acid conjugates that catalyze both syn- and anti-aldol reactions of dihydroxyacetones (DHAs) with high diastereoselectivities and enantioselectivities.	diamine-bronsted acid	42-63	synemin	Homo sapiens	94-97
21359299-2	2011	These new primary-tertiary diamine-Bronsted acid conjugates bifunctional organocatalysts efficiently catalyzes the asymmetric direct syn selective cross-aldol reaction of different protected hydroxyacetone with various aldehydes in high yield (94%) and high enantioselectivity (up to 97% ee of syn) and dr of 91 : 9 (syn/anti) under mild reaction conditions.	diamine-bronsted acid	27-48	synemin	Homo sapiens	294-297
21359299-2	2011	These new primary-tertiary diamine-Bronsted acid conjugates bifunctional organocatalysts efficiently catalyzes the asymmetric direct syn selective cross-aldol reaction of different protected hydroxyacetone with various aldehydes in high yield (94%) and high enantioselectivity (up to 97% ee of syn) and dr of 91 : 9 (syn/anti) under mild reaction conditions.	diamine-bronsted acid	27-48	synemin	Homo sapiens	294-297
20521772-2	2010	To achieve this end, chiral primary amines have been explored and the primary-tertiary diamine-Bronsted acid salts are found to promote the cross-aldol reactions of aldehydes with high activity and syn selectivity.	diamine-bronsted acid	87-108	synemin	Homo sapiens	198-201