17136-56-0

Upstream product

• 5854-97-7 D,L-2-Benzoylamino-3--propionsaeure 
• 42492-83-1 C₂₃H₂₁N₃O₄ 
• 52245-18-8 DL-2-Amino-3-(N-tosyl-N-2,4,6-trimethylbenzyloxy)-aminopropionsaeure 
• 87333-22-0 3-chloro-2-acetylamino-propionic acid methylester 

Downstream Products

• 5854-95-5 D,L-Alanosin 
• 5854-97-7 D,L-2-Benzoylamino-3--propionsaeure 
• 5854-93-3 Alanosine 

Relevant academic research and scientific papers

Biosynthesis of the N–N-Bond-Containing Compound l-Alanosine

The formation of a N?N bond is a unique biochemical transformation, and nature employs diverse biosynthetic strategies to activate nitrogen for bond formation. Among molecules that contain a N?N bond, biosynthetic routes to diazeniumdiolates remain enigma

Process for producing N-alkylhydroxylamines

A novel process for producing an N-alkylhydroxylamine of the formula (I) wherein R represents an alkyl group which may be substituted with least one substituent, which comprises reacting an N-mesyl-O-(p-alkoxybenzyl)hydroxylamine or an N-mesyl-O-(2,4,6-trialkylbenzyl)hydroxylamine with an alkyl halide of the formula (III) wherein R is as defined above and X represents a halogen atom, under a basic condition to produce the corresponding N-alkyl-N-mesyl-O-(p-alkoxybenzyl)hydroxylamine or N-alkyl-N-mesyl-O-(2,4,6-trialkylbenzyl)hydroxylamine, and treating the resulting compound with a solution of a phenol compound, and novel N-alkyl-N-mesyl-O-(p-alkoxybenzyl)hydroxyl amines and N-alkyl-N-mesyl-O-(2,4,6-trialkylbenzyl)hydroxylamines which are useful as intermediates in the above process.