749926-98-5

Upstream product

• 26429-97-0 methyl (2E)-5-phenyl-2-pentenoate 
• 75553-23-0 (E)-5-phenyl-2-penten-1-ol 
• 104-53-0 3-phenyl-propionaldehyde 
• 160805-54-9 (E)-tert-butyldimethyl((5-phenylpent-2-en-1-yl)oxy)silane 

Downstream Products

• 749926-99-6 1-(tert-butyl-dimethyl-silanyl)-5-phenyl-pent-2-en-1-one 
• 749927-02-4 (2S,3R)-2-Amino-3-phenethyl-pent-4-enoic acid 
• 749927-12-6 (E)-(S)-1-(tert-Butyl-dimethyl-silanyl)-5-phenyl-pent-2-en-1-ol 
• 749927-03-5 (2S,3R)-2-tert-Butoxycarbonylamino-3-phenethyl-pent-4-enoic acid methyl ester 
• 749927-00-2 tert-butoxycarbonylamino-acetic acid 1-(tert-butyl-dimethyl-silanyl)-5-phenyl-pent-2-enyl ester 
• 749927-01-3 2-tert-butoxycarbonylamino-5-(tert-butyl-dimethyl-silanyl)-3-phenethyl-pent-4-enoic acid 

Relevant academic research and scientific papers

Synthesis of optically active β-alkyl aspartate via [3,3] sigmatropic rearrangement of α-acyloxytrialkylsilane

The synthesis of four types of optically active β-carbon-substituted analogs of threo-β-hydroxy aspartate (THA) and a β-carbon-substituted analog of threo-β-benzyloxy aspartate (TBOA), which are potent blockers of excitatory amino acid transporters in the