38846-00-3

Upstream product

• 2568-65-2 N,N-dimethyl-3-phenyl-2-propyn-1-amine 
• 4392-24-9 Cinnamyl bromide 
• 536-74-3 phenylacetylene 

Downstream Products

• 75376-89-5 1-phenyl-NN,2-trimethyl-3-naphthylmethylamine 
• 75376-88-4 2-(Dimethylaminomethyl)-3-methyl-1-phenylnaphthalene 
• 75377-01-4 3a,4-dihydro-2,2-dimethyl-4-phenylbenzisoindolinium bromide 
• 92-94-4 [1,1';4',1'']terphenyl 
• 38846-06-9 3-(dimethylamino)-1,4-diphenylhex-5-en-1-yne 
• 38846-12-7 3-dimethylamino-1,6-diphenylhex-5-en-1-yne 
• 38846-06-9 3-dimethylamino-1,4-diphenylhex-5-en-1-yne 
• 38846-06-9 3-dimethylamino-1,4-diphenylhex-5-en-1-yne 
• 38846-12-7 3-dimethylamino-1,6-diphenylhex-5-en-1-yne 

Relevant academic research and scientific papers

Base Catalysed Rearrangements involving Ylide Intermediates. Part 1. The Rearrangements of Diallyl- and Allylpropynyl-ammonium Cations

The base catalysed rearrangements of diallylammonium cations and allylpropynylammonium cations are described.In most cases, the major product arises by a symmetry-allowed sigmatropic rearrangement of the intermediate ylide.The minor products can be regarded as being derived by homolysis of the ylide into a radical pair followed by recombination.