89063-96-7

Upstream product

• 4556-23-4 pyridine-4-thiol 
• 89063-94-5 4-nitrobenzyl (2R,5R,6R)-3,7-dioxo-6-(1-methoxy-1-methylethyl)-1-azabicyclo<3.2.0>heptane-2-carboxylate 
• 86541-17-5 (6R)-2,2-dimethyl-3-oxa-1-azabicyclo<4.2.0>octan-8-one 
• 89063-93-4 4-nitrobenzyl (2R,3R)-2-diazo-4-<3-(1-methoxy-1-methylethyl)-4-oxoazetidin-2-yl>-3-oxobutanoate 
• 89063-91-2 (2R,3R)-2-<3-(1-methoxy-1-methylethyl)-4-oxoazetidin-2-yl>acetic acid 
• 89001-88-7 (6R,7S)-2,2-dimethyl-7-(1-methoxy-1-methylethyl)-1-aza-3-oxabicyclo<4.2.0.>octan-8-one 
• 89063-92-3 4-nitrobenzyl (2R,3R)-4-<3-(1-methoxy-1-methylethyl)-4-oxoazetidin-2-yl>-3-oxobutanoate 
• 7087-68-5 N-ethyl-N,N-diisopropylamine 

Relevant academic research and scientific papers

1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid derivatives

Compounds of the formula [I] STR1 in which R1 is hydroxy, a protected hydroxy or lower alkoxy group, R2 is carboxy or an easily eliminable esterified carboxy group and R3 is pyridyl, and pharmaceutically acceptable salts t

SYNTHETIC STUDIES ON CARBAPENEM ANTIBIOTICS FROM PENICILLINS. VI. SYNTHESES OF OPTICALLY ACTIVE O-METHYLCARPETIMYCIN AND O-METHYL-6-EPICARPETIMYCIN

The syntheses of the optically active O-methylcarpetimycin 2a and O-methyl-6-epicarpetimycin 2b were achieved by a route involving one-pot syntheses of 5a and 5b from 3.