14689-79-3

Upstream product

• 551-16-6 6-Aminopenicillanic Acid 
• 90-02-8 salicylaldehyde 
• 21794-93-4 6-aminopenicillanic acid 
• 105-13-5 4-Methoxybenzyl alcohol 

Downstream Products

• 21008-47-9 6β-(2-hydroxy-benzylideneamino)-penicillanic acid methyl ester 
• 47547-28-4 6-aminopenicillanic acid diphenylmethyl ester 
• 87417-35-4 5-[(1R,5R)-6-((R)-1-Benzhydryloxycarbonyl-2-methyl-allyl)-7-oxo-4-thia-2,6-diaza-bicyclo[3.2.0]hept-2-en-3-yl]-2-tert-butoxycarbonylamino-pentanoic acid benzhydryl ester 
• 87417-35-4 (S)-5-[(1S,5S)-6-((R)-1-Benzhydryloxycarbonyl-2-methyl-allyl)-7-oxo-4-thia-2,6-diaza-bicyclo[3.2.0]hept-2-en-3-yl]-2-tert-butoxycarbonylamino-pentanoic acid benzhydryl ester 
• 87408-06-8 5-[(1R,5R)-6-((R)-1-Benzhydryloxycarbonyl-2-methyl-propyl)-7-oxo-4-thia-2,6-diaza-bicyclo[3.2.0]hept-2-en-3-yl]-2-tert-butoxycarbonylamino-pentanoic acid benzhydryl ester 
• 87408-06-8 (S)-5-[(1S,5S)-6-((R)-1-Benzhydryloxycarbonyl-2-methyl-propyl)-7-oxo-4-thia-2,6-diaza-bicyclo[3.2.0]hept-2-en-3-yl]-2-tert-butoxycarbonylamino-pentanoic acid benzhydryl ester 
• 87408-05-7 (2S,5R,6R)-6-(5-Benzhydryloxycarbonyl-5-tert-butoxycarbonylamino-pentanoylamino)-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester 
• 87408-05-7 iso-penicillin N 
• 87417-34-3 (2S,5R,6R)-6-(5-Benzhydryloxycarbonyl-5-tert-butoxycarbonylamino-pentanoylamino)-3,3-dimethyl-4,7-dioxo-4λ⁴-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester 
• 87417-34-3 benzhydryl N-δ--6-aminopenicillanate β-sulfoxide 
• 60750-63-2 N-salycilidene-6-aminopenicillanic acid, p-methoxy-benzyl ester 
• 87417-35-4 (S)-5-[(1R,5R)-6-((R)-1-Benzhydryloxycarbonyl-2-methyl-allyl)-7-oxo-4-thia-2,6-diaza-bicyclo[3.2.0]hept-2-en-3-yl]-2-tert-butoxycarbonylamino-pentanoic acid benzhydryl ester 
• 87408-06-8 (S)-5-[(1R,5R)-6-((R)-1-Benzhydryloxycarbonyl-2-methyl-propyl)-7-oxo-4-thia-2,6-diaza-bicyclo[3.2.0]hept-2-en-3-yl]-2-tert-butoxycarbonylamino-pentanoic acid benzhydryl ester 

Relevant academic research and scientific papers

CONCERNING THE INTERMEDIACY OF MONOCYCLIC β-LACTAMS IN PENICILLIN BIOSYNTHESIS: SYNTHESIS AND ATTEMPTED BIOCONVERSION OF SECO-ISOPENICILLIN N

The title compound (3a) was synthesized as its dimer by the skeletal rearrangement of protected isopenicillin N-sulfoxide, hydrogenation, hydrolysis of the thiazoline ring, oxidative dimerization and deprotection.The reductive conversion of the dimer to m

1-Oxides of Schiff bases of 6-aminopenicillanic acid

Compounds containing a cephem nucleus are prepared by heating a 1-oxide of a Schiff base of 6-aminopenicillanic acid. These cephem compounds are useful as intermediates in the preparation of physiologically active cephalosporins.