749261-84-5

Upstream product

• 275808-71-4 (R)-3-Hydroxy-7-methyl-oct-6-enoic acid methoxy-methyl-amide 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 36255-44-4 3-bromopropanal dimethyl acetal 
• 881660-85-1 (1S)-4-nitrobenzoic acid 1-[(2S)-2-azido-5,5-dimethoxypentyl]-5-methylhex-4-enyl ester 
• 881660-84-0 (1R)-propionic acid 1-[(2R)-2-hydroxy-5,5-dimethoxypentyl]-5-methylhex-4-enyl ester 
• 881660-83-9 (R)-6-Hydroxy-1,1-dimethoxy-10-methyl-undec-9-en-4-one 
• 725724-04-9 (R)-3-benzyloxybutyl p-toluenesulfonate 
• 116757-62-1 (R)-3-O-benzyl-1,3-butanediol 
• 881660-87-3 4-Nitro-benzoic acid (E)-(1S,7R)-1-((S)-2-azido-5,5-dimethoxy-pentyl)-7-benzyloxy-oct-4-enyl ester 
• 881660-86-2 4-Nitro-benzoic acid (1S,3S)-3-azido-6,6-dimethoxy-1-(3-oxo-propyl)-hexyl ester 
• 749261-52-7 (1R)-propionic acid 1-[(2S)-2-azido-5,5-dimethoxypentyl]-5-methylhex-4-enyl ester 
• 749261-55-0 5-[(3R)-3-benzyloxybutane-1-sulfonyl]-1-phenyl-1H-tetrazole 

Relevant academic research and scientific papers

Evolution of a strategy for the synthesis of structurally complex batzelladine alkaloids. Enantioselective total synthesis of the proposed structure of batzelladine F and structural revision

Stereoselective synthesis of octahydro-5,6,6a-triazaacenaphthalenes 29 and 34 having the anti-relationship of the angular hydrogens flanking the pyrrolidine nitrogen confirmed suspicions that the relative configuration of the left-hand tricyclic guanidine

Inhibition of HIV-1 envelope-mediated fusion by synthetic batzelladine analogues

Marine natural products that feature polycyclic guanidine motifs, such as crambescidins and batzelladines, are known to have antiviral activities toward some viruses including HSV and HIV. In this study we evaluated a synthetic library containing 28 batze