886355-68-6

Upstream product

• 96-32-2 bromoacetic acid methyl ester 
• 198021-44-2 (3S,4R)-1-[bis(trimethylsilyl)methyl]-4-methyl-3-[(4S,5R)-4,5-diphenyl-2-oxo-oxazolidin-3-yl]-azetidin-2-one 
• 100-39-0 benzyl bromide 
• 813440-34-5 (3R,4R)-3-benzyl-1-[bis(trimethylsilyl)methyl]-4-methyl-3-[(4S,5R)-4,5-diphenyl-2-oxo-oxazolidin-3-yl]-azetidin-2-one 
• 813440-43-6 (3R,4R)-3-benzyl-1-[bis(trimethylsilyl)methyl]-3-(tert-butoxycarbonylamino)-4-methylazetidin-2-one 

Relevant academic research and scientific papers

Synthesis of type II β-turn surrogate dipeptides based on syn-α-amino-α,β-dialkyl-β-lactams

(Chemical equation presented) The achiral bis(trimethylsilyl)methyl group acts as an efficient stereochemical determinant of the α-alkylation reaction in β-branched α-phenyloxazolidinyl- or α- diphenyloxazolidinyl-β-lactams and provides the first stereoco