368448-97-9

Upstream product

• 368448-91-3 methyl (3R,4E,αS)-3-(N-benzyl-N-α-methylbenzylamino)-5-phenylpent-4-enoate 
• 170726-18-8 methyl (3S)-3-amino-5-phenylpentanoate 
• 158807-52-4 methyl (3S)-3-(N-tert-butoxycarbonylamino)-5-phenylpentanoate 
• 38447-05-1 (2E,4E)-methyl 5-phenylpenta-2,4-dienoate 
• 368448-95-7 methyl (3R,4E)-3-(N-tert-butoxycarbonylamino)-5-phenylpent-4-enoate 

Downstream Products

• 368448-99-1 (3R,4E)-3-amino-5-phenylpent-4-enoic acid 

Relevant academic research and scientific papers

In situ generation of N -Boc-protected alkenyl imines: Controlling the e / Z geometry of alkenyl moieties in the Mukaiyama-Mannich reaction

Readily available Boc-protected Z-alkenyl aminals could be used as Z-alkenyl and E-alkenyl imine precursors under acidic conditions. In the Mukaiyama-Mannich reaction of Z-alkenyl Boc-aminals, the E/Z geometry of the products was controlled by the catalys

Serine-threonine protein phosphatase inhibitors derived from nodularin: Role of the 2-methyl and 3-diene groups in the Adda residue and the effect of macrocyclic conformational restraint

In order to probe the effect upon macrocycle conformation and PP1cat enzyme inhibition of structural changes to nodularin, specific replacements for the Adda residue were introduced. Two new analogues, cyclo[-(3S,E)-3-phenylethenyl-3-aminopropa