286949-15-3

Upstream product

• 100-39-0 benzyl bromide 
• 286949-40-4 [1-(2-benzyloxy-ethyl)-allyl]-carbamic acid tert-butyl ester 
• 286949-39-1 1-(1,1-dimethylethoxy)-N-(1-(2-hydroxyethyl)-2-propenyl)methanamide 
• 286949-14-2 (S)-1-(2-Benzyloxy-ethyl)-allylamine 
• 286949-41-5 [(S)-1-(2-Benzyloxy-ethyl)-allyl]-cyclopentylidene-amine 
• 1730-25-2 allylmagnesium bromide 

Downstream Products

• 286949-33-5 (1-Allyl-cyclopentyl)-[(S)-1-(2-benzyloxy-ethyl)-allyl]-carbamic acid methyl ester 

Relevant academic research and scientific papers

An imine addition/ring-closing metathesis approach to the spirocyclic core of halichlorine and pinnaic acid.

[reaction: see text] An approach to the spirocyclic core of halichlorine and pinnaic acid has been designed around an imine allylation/ring-closing metathesis sequence. This sequence has been used to generate several azabicylo[n.5] model systems. A newly