7.7
[]. Brian A Sparling, et al. SmI2-promoted Reformatsky-type coupling reactions in exceptionally hindered contexts. Org Lett. 28 Mar 2;(6):29-4.
[2]. D L Hallahan, et al. Synthesis and biological activity of an azido derivative of paclobutrazol, an inhibitor of gibberellin biosynthesis. Plant Physiol. 988 Dec;88(4):425-9.
[3]. E Salih, et al. Active-site peptides of acetylcholinesterase of Electrophorus electricus: labelling of His-44 by -bromo-[2-4C]pinacolone and Ser-2 by tritiated diisopropyl fluorophosphate. Biochim Biophys Acta. 994 Oct 9;28(2):324-3.
[4]. S G Cohen, et al. -Bromopinacolone, an active site-directed covalent inhibitor for acetylcholinesterase. J Biol Chem. 982 Dec ;257(23):487-92.
[5]. S G Cohen, et al. Reactions of -bromo-2-[4C]pinacolone with acetylcholinesterase from Torpedo nobiliana. Effects of 5-trimethylammonio-2-pentanone and diisopropyl fluorophosphate. Biochim Biophys Acta. 989 Aug 3;997(3):67-75.
H32-H35-H39-H335
P26-P264-P27-P27-P28-P32+P352-P34+P34-P35+P35+P338-P33-P362+P364-P43+P233-P45-P5
GHS7