286949-31-3

Upstream product

• 79-22-1 methyl chloroformate 
• 286949-25-5 allyl-(1-allyl-cyclohexyl)-amine 
• 108-94-1 cyclohexanone 
• 6115-03-3 N-Cyclohexylideneallylamine 
• 1670-99-1 1-((methoxycarbonyl)amino)cyclohexane-1-carboxylic acid 
• 286949-37-9 allyl-(4-tert-butyl-cyclohexylidene)-amine 
• 1730-25-2 allylmagnesium bromide 
• 76403-35-5 methyl (1-prop-2-en-1-ylcyclohexyl)carbamate 
• 106-95-6 allyl bromide 
• 2756-85-6 1-aminocyclohexane carboxylic acid 

Relevant academic research and scientific papers

Synthesis of alkaloid analogues from α-amino acids by one-pot radical decarboxylation/alkylation

A mild, one-pot methodology to obtain α-substituted nitrogen heterocycles from commercial amino acids is reported. This versatile procedure has been applied to the synthesis of different alkaloid analogues in good to excellent yields. Wiley-VCH Verlag GmbH & Co. KGaA, 2005.

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