38015-96-2

Upstream product

• 38015-83-7 2,2,2-trichloroethyl (1S,3S,5R,6R,2'S)-6-(2'-bromo-2'-phenylacetamido)-2,2-dimethylpenam-3-carboxylate, 1-oxide 
• 39879-59-9 2,2,2-trichloroethyl (1S,3S,5R,6R)-6-phenylacetamido-2,2-dimethylpenam-3-carboxylate, 1-oxide 
• 38015-90-6 2,2,2-trichloroethyl (1S,3S,5R,6R,2'R)-6-(2'-azido-2'-phenylacetamido)-2,2-dimethylpenam-3-carboxylate, 1-oxide 

Downstream Products

• 52749-46-9 6β-((R)-2-amino-2-phenyl-acetylamino)-penicillanic acid 2,2,2-trichloro-ethyl ester 
• 38016-00-1 2,2,2-trichloroethyl (1S,3S,5R,6R,2'R)-6-(2'-phenyl-2'-<2,2,2-trichloroethoxycarbonylamino>acetamido)-2,2-dimethylpenam-3-carboxylate 
• 1261-18-3 D-ampicillin hydrogen naphthalene-2-sulphonate 
• 38015-98-4 2,2,2-trichloroethyl (1S,3S,5R,6R,2'R)-6-(2'-phenyl-2'-<2,2,2-trichloroethoxycarbonylamino>acetamido)-2,2-dimethylpenam-3-carboxylate, 1-oxide 

Relevant academic research and scientific papers

Synthesis of functionalized penicillins and cephalosporins by photo-initiated bromination. A novel route to ampicillin and cephalexin from penicillin G

Potoinitiated bromination of the 1S-oxide ester 9, available in two stages from penicillin G6, gave the diastereometic bromides 10a and 10b. Both isomers have been utilized in further transformations to give the established antibiotics ampicillin 7 and cephalexin 8.