80662-87-9

Upstream product

• 108-24-7 acetic anhydride 
• 25070-76-2 benzyl diallylcarbamate 
• 34637-22-4 3-[(N-benzyloxycarbonyl)amino]propanol 
• 75-36-5 acetyl chloride 
• 627-18-9 1-bromo-3-propanol 
• 69261-50-3 N-(benzyloxycarbonyl)acetamide 
• 621-84-1 O-benzyl carbamate 

Relevant academic research and scientific papers

Benzyl Acetylcarbamate Potassium Salt (BENAC-K): A Simple Nucleophilic N -Acetamide Equivalent

Benzyl acetylcarbamate potassium salt (BENAC-K) has been developed as a simple nucleophilic acetamide equivalent. A broad variety of alkyl halides were converted into benzyloxycarbonyl-protected N -alkylacetamides in high yields by simple treatment with an almost equimolar (1.1 equiv) amount of BENAC-K in a polar solvent.

N-acyl acidic amino acid diamide derivative, a salt thereof, and an anti-ulcer agent containing the same

This invention relates to a novel N-acyl acidic amino acid diamide derivative represented by the general formula or a salt thereof: STR1 wherein each of R1, R2, R3 and R4, which may be the same or different, rep

Hydroboration-Carbon Monoxide Insertion of Bis-Olefinic Amine Derivatives. Synthesis of δ-Coniceine, Pyrrolizidine, (+/-)-Heliotridane, and (+/-)-Pseudoheliotridane

The hydroboration-carbon monoxide insertion of several bis-olefinic derivatives has provided facile preparations of N-(carbomethoxy)-5-azacyclooctanone (6), N-(carbobenzyloxy)-5-azacyclooctanone (9), and N-(carbobenzyloxy)-5-cyclononanone (18).Of the hydroboration protocols examined, thexylborane-cyanidation proved to be the most useful.Reductive ring closure of 9 and of 18 gave 26 and 27, respectively.Methylation of 9 followed by reduction afforded 29 and 30.