659747-12-3

Upstream product

• 1025826-61-2 C₁₅H₂₄N₄O₇ 
• 659747-10-1 Boc₂-Asp(OBn)-OMe 
• 176755-21-8 N-bis-(tert-butoxycarbonyl)aspartic acid α-methyl ester 
• 80963-12-8 4-benzyl 1-methyl N-(tert-butoxycarbonyl)-L-aspartate 
• 7536-58-5 BOC-L-aspartic acid 4-benzyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 61040-22-0 N^β-benzyloxycarbonyl-N^α-Boc-(S)-β-aminoalanine methyl ester 
• 65710-57-8 3-{[(benzyloxy)carbonyl]amino}-N-(tert-butoxycarbonyl)-L-alanine 
• 87768-65-8 N-β-Z-L-diaminopropionic acid methyl ester 

Relevant academic research and scientific papers

An Efficient Synthesis of a Probe for Protein Function: 2,3-Diaminopropionic Acid with Orthogonal Protecting Groups

(Matrix presented) An efficient and cost-effective synthesis of N(α)-Boc2-N(β)-Cbz-2,3-diaminopropionic acid is reported. The synthesis starts from commercially available N(α)-Boc-Asp(OBn)-OH and employs a Curtius rearrangement to establish the β-nitrogen. Proper protection of the α-nitrogen is essential for the success of the Curtius rearrangement.