136353-99-6

Upstream product

• 67-56-1 methanol 
• 69261-51-4 Isobutyryl-carbamic acid benzyl ester 
• 1149-26-4 (S)-N-(benzyloxycarbonyl)valine 

Downstream Products

• 136401-31-5 [(S)-2-Methyl-1-((S)-5-oxo-2,5-dihydro-furan-2-yl)-propyl]-carbamic acid benzyl ester 
• 136401-31-5 [(S)-2-Methyl-1-((R)-5-oxo-2,5-dihydro-furan-2-yl)-propyl]-carbamic acid benzyl ester 
• 147169-18-4 benzyl N-<1-((p-methylphenyl)sulfonyl)-2-methypropyl>carbamate 
• 130457-30-6 benzyl N-[1-(1,2,3-benzotriazol-1-yl)-2-methylpropyl]carbamate 

Relevant academic research and scientific papers

Non-Kolbe electrolysis of

Here, we report a standardized method for the synthesis of N-protected (1-methoxyalkyl)amines by the electrochemical decarboxylative α-methoxylation of α-amino acid derivatives using the commercially available, easy-to-use, compact ElectraSyn 2.0 setup. T

Catalyst-free Mannich-type reaction of 1-(N-acylamino)alkyltriphenylphosphonium salts with silyl enolates

A catalyst-free reaction of 1-(N-acylamino)alkyltriphenylphosphonium tetrafluoroborates with silyl enolates was developed to prepare β-amino carbonyl compounds. The reported method is a useful approach for the preparation of N-protected β-amino esters as