89088-15-3

Upstream product

• 72978-15-5 3-Brom-1-pyrrolin-2-carbonsaeure-methylester 
• 89088-14-2 N-(tert-Butoxycarbonyl)-L-phenyl-alanyltyramide 
• 51-67-2 tyrosamine 
• 3674-06-4 (tert-butoxycarbonyl)-L-phenylalanine N-hydroxysuccinimide ester 

Downstream Products

• 89088-16-4 Sodium 3-amino>ethyl>phenoxy>-1-pyrroline-2-carboxylate 
• 89088-33-5 (5S,8RS,9RS)-N^α,9-Ethylene-5-benzyl-N⁸-carbobenzoxy-1,2-dihydro-p-phencyclopeptine 
• 89088-29-9 p-Nitrophenyl N-Carbobenzoxy-trans-β-amino>ethyl>phenoxy>prolinate 
• 89088-32-4 3-{4-[2-(2-Amino-3-phenyl-propionylamino)-ethyl]-phenoxy}-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-(4-nitro-phenyl) ester; compound with trifluoro-acetic acid 
• 89088-17-5 trans-N-Carbobenzoxy-β-amino>ethyl>phenoxy>proline 
• 89088-28-8 (2S,3S)-3-{4-[2-((S)-2-tert-Butoxycarbonylamino-3-phenyl-propionylamino)-ethyl]-phenoxy}-1-[2-(2-dimethylamino-propionylamino)-3-methyl-butyryl]-pyrrolidine-2-carboxylic acid 
• 89088-28-8 (2R,3R)-3-{4-[2-((S)-2-tert-Butoxycarbonylamino-3-phenyl-propionylamino)-ethyl]-phenoxy}-1-[2-(2-dimethylamino-propionylamino)-3-methyl-butyryl]-pyrrolidine-2-carboxylic acid 
• 89105-91-9 trans-β-amino>ethyl>phenoxy>proline 
• 82784-33-6 Dihydromauritine A 
• 82837-87-4 (5S,8R,9R)-5-Benzyl-1,2-dihydro-N^α-(N,N-dimethyl-L-alanyl-L-valyl)-N^α,9-ethylene-p-phencyclopeptine 

Relevant academic research and scientific papers

Synthesis of Dihydromauritine A, a Reduced Cyclopeptide Alkaloid

The synthesis of the strained 14-membered cyclopeptide alkaloid derivative dihydromauritine A has been accomplished from L-proline via SN2 displacement and three amide bond forming steps.The nucleophilic displacement involved a β-bromopyrroline