752251-07-3

Upstream product

• 752251-06-2 (S)-3-amino-6,7-bis(OBn)-1,1-dimethyl-1,2,3,4-tetrahydroquinolin-1-ium L-ser(OBn)-D-ser (OBn)-BocL-thr(OBn) 
• 59-92-7 levodopa 
• 15260-10-3 N-Boc-O-benzyl-L-threonine 
• 84907-81-3 (2R)-3-benzyloxy-2-aminopropanoic acid methyl ester 
• 67389-47-3 (R)-3-benzyloxy-2-tert-butoxycarbonyl-amino-propionic acid methyl ester 
• 862695-37-2 4-((S)-2-Amino-3-dimethylamino-propyl)-benzene-1,2-diol 
• 752251-02-8 (S)-[2-(3,4-dihydroxy-phenyl)-1-dimethylcarbamoyl-ethyl]-carbamic acid tert-butyl ester 
• 752251-05-1 (2S,3S)-6,7-bis-benzyloxy-3-(3-benzyloxy-2-tert-butoxycarbonylaminopropionylamino)-1,1-dimethyl-1,2,3,4-tetrahydroquinolinium 
• 752251-19-7 (S)-3-((S)-2-Amino-3-benzyloxy-propionylamino)-6,7-bis-benzyloxy-1,1-dimethyl-1,2,3,4-tetrahydro-quinolinium 
• 752251-00-6 (2S,3S)-3-(3-benzyloxy-2-tert-butoxycarbonylamino-propionylamino)-6,7-dihydroxy-1,1-dimethyl-1,2,3,4-tetrahydro-quinolinium 
• 752251-04-0 (S,S)-{2-benzyloxy-1-[1-(3,4-dihydroxy-benzyl)-2-dimethylamino-ethylcarbamoyl]-ethyl}-carbamic acid tert-butyl ester 
• 752251-20-0 (2R)-3-benzyloxy-2-((2S)-3-benzyloxy-2-tert-butoxycarbonylamino-butyrylamino)propionic acid 
• 752251-21-1 (2R)-3-benzyloxy-2-((2S)-3-benzyloxy-2-tert-butoxycarbonylamino-butyrylamino)propionic acid methyl ester 

Relevant academic research and scientific papers

Allelopathic Activity of the Iron Chelator Anachelin?–?A Molecular Hybrid with a Dual Mode of Action

One of the compounds suggested to be responsible for the cyanobacterial dominance over competing green algae is identified. Evidence is provided on the molecular, chemical level that the iron chelator anachelin from the cyanobacterium Anabaena cylindrica promotes both the growth of cyanobacteria and reduces the growth of competing chlorophytes. These results illustrate a molecular strategy of addressing two challenges (nutrient availability and algal competition) by one molecule. Such strategies could be implied in harmful algal blooms in marine and freshwater environments.

A biomimetic route to the peptide alkaloid anachelin

A postulated biogenesis forms the basis for a synthetic route to the natural product anachelin H (1). Key steps include a tellurium-mediated, oxidative aza annulation and a Claisen condensation under mild conditions. Experiments with a model substrate ind