895138-20-2

Upstream product

• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 19740-90-0 (Z)-9-oxabicyclo[6.1.0]non-4-ene 
• 895138-16-6 (1S,2S,6S)-(+)-9-[(R)-1-phenylethyl]-9-azabicyclo[4.2.1]nonan-2-ol 

Downstream Products

• 895138-22-4 (1S,6S)-3-allyl-9-[(R)-1-phenylethyl]-9-azabicyclo[4.2.1]nonan-2-one 
• 353461-15-1 tert-butyl (1S,6S)-2-oxo-9-azabicyclo[4.2.1]nonane-9-carboxylate 
• 895138-24-6 (1S,6S)-3-allyl-9-[(R)-1-phenylethyl]-9-azabicyclo[4.2.1]nonane-2-carbonitrile 
• 895138-27-9 (1S,6S)-9-[(R)-1-phenylethyl]-pyrido[3,4-b]homotropane 
• 895138-26-8 (1S,6S)-3-allyl-9-[(R)-1-phenylethyl]-9-azabicyclo[4.2.1]nonane-2-carbaldehyde 

Relevant academic research and scientific papers

A unified approach to the synthesis of both enantiomers of anatoxin-a and homoanatoxin-a cyanotoxins

Anatoxin-a and homoanatoxin-a are highly neurotoxic compounds produced by cyanobacteria, principally during surface water-blooms (SWBs). Owing to their powerful biological activity and unique structural characteristics, these natural alkaloids have been t

Synthesis and pharmacological characterization of nicotinic acetylcholine receptor properties of (+)- and (-)-pyrido-[3,4-b]homotropanes

(±)-Pyrido[3,4-b]homotropane [(±)-1] is a conformationally rigid analogue of nicotine (2) or nornicotine (3) that showed high affinity for nicotinic acetylcholine receptors. Even though the synthesis and potent activity of this highly interesting compound