Chemical Reagents

(R)-tert-Butyl 3-phenylpiperazine-1-carboxylate.

(R)-tert-butyl 4-aminobutan-2-ylcarbamate.

(R)-Tetrahydro-3-furoic acid

(R，S)-2-Isobutyl-3-(boc-amino)propanoic acid.

(R，S)-2-Isobutyl-3-(boc-amino)propanoic acid.

Application ( R , S )-AM1241 has been used as a cannabinoid CB2 agonist: to study its inhibitory effect on bone cancer-induced pain and bone loss to study the effect of its interaction with 17&#946estradiol on proliferation activity in primary

Application ( R , S )-AM1241 has been used as a cannabinoid CB2 agonist: to study its inhibitory effect on bone cancer-induced pain and bone loss to study the effect of its interaction with 17&#946estradiol on proliferation activity in primary

Application The following hydroxamic acid catalyst was shown by Bode and coworkers to assist in the kinetic resolution of cyclic amines through acylation of one enantiomer, which can be controlled using either the ( R or S )- or ( S or R )-Bode

Application Enantioselective allylic substitution, enantioselective 1,3-dipolar cycloaddition.

Application Enantioselective allylic substitution, enantioselective 1,3-dipolar cycloaddition.

Application ( S )-(+)-1,2-Propanediol can be used as a reactant to synthesize: Optically active chiral ( S )-1, 2-propanediol derivatives using mesogenic carboxylic acids via esterification in the presence of dimethylaminopyridine (DMAP) as a

Application ( S )-(+)-1,2-Propanediol can be used as a reactant to synthesize: Optically active chiral ( S )-1, 2-propanediol derivatives using mesogenic carboxylic acids via esterification in the presence of dimethylaminopyridine (DMAP) as a