500800-65-7

Upstream product

• 627079-33-8 2-aminooxy-3-phenyl-propionic acid tert-butyl ester 
• 380886-35-1 D-tert-butyl 2-phthalimid-N-oxy-4-methylpentanoate 
• 310404-45-6 (R)-4-methyl-2-phthalimidooxypentanoic acid 
• 500800-63-5 (S)-2-[(R)-2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yloxy)-4-methyl-pentanoylaminooxy]-3-phenyl-propionic acid tert-butyl ester 

Downstream Products

• 627079-37-2 (S)-2-[(R)-2-((R)-2-Benzyloxycarbonylamino-propionylaminooxy)-4-methyl-pentanoylaminooxy]-3-phenyl-propionic acid tert-butyl ester 
• 627079-36-1 (S)-2-[(R)-2-((S)-2-Benzyloxycarbonylamino-propionylaminooxy)-4-methyl-pentanoylaminooxy]-3-phenyl-propionic acid tert-butyl ester 
• 627079-35-0 (S)-2-[(R)-2-(2-Benzyloxycarbonylamino-acetylaminooxy)-4-methyl-pentanoylaminooxy]-3-phenyl-propionic acid tert-butyl ester 
• 500800-66-8 (S)-2-((R)-2-{(S)-2-[(R)-2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yloxy)-4-methyl-pentanoylaminooxy]-3-phenyl-propionylaminooxy}-4-methyl-pentanoylaminooxy)-3-phenyl-propionic acid tert-butyl ester 
• 500800-67-9 (S)-2-{(R)-2-[(S)-2-((R)-2-Aminooxy-4-methyl-pentanoylaminooxy)-3-phenyl-propionylaminooxy]-4-methyl-pentanoylaminooxy}-3-phenyl-propionic acid tert-butyl ester 
• 500800-68-0 (S)-2-[(R)-2-((S)-2-{(R)-2-[(S)-2-((R)-2-Aminooxy-4-methyl-pentanoylaminooxy)-3-phenyl-propionylaminooxy]-4-methyl-pentanoylaminooxy}-3-phenyl-propionylaminooxy)-4-methyl-pentanoylaminooxy]-3-phenyl-propionic acid tert-butyl ester 
• 500800-60-2 2-{2-[2-(2-{2-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-4-methyl-pentanoylaminooxy]-3-phenyl-propionylaminooxy}-4-methyl-pentanoylaminooxy)-3-phenyl-propionylaminooxy]-4-methyl-pentanoylaminooxy}-3-phenyl-propionic acid tert-butyl ester 

Relevant academic research and scientific papers

A Reverse Turn Structure Induced by a D,L-α-Aminoxy Acid Dimer

Our previous work revealed that two adjacent D-α-aminoxy acids could form two homochiral N-O turns, with the backbone folding into an extended helical structure (1.88-helix). Here, we report the conformational studies of linear peptides 3-6, wh

Cyclic hexapeptide of D,L-α-aminoxy acids as a selective receptor for chloride ion

Cyclic hexapeptide 2, prepared from linear hexapeptide 1 of alternating D- and L-α-aminoxy acids, was found to adopt a C3 symmetric and bracelet-like conformation with consecutive eight-membered-ring hydrogen bonds (N-O turns) in nonpolar solve