85738-05-2

Upstream product

• 122-78-1 phenylacetaldehyde 
• 135663-97-7 1-phenylbut-3-yn-2-ol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 85738-06-3 N-(1-benzylprop-2-ynyl)benzylamine 
• 85738-21-2 N,9α-dibenzyl-cis-8-azabicyclo<4.3.0>non-4-en-7-one 
• 85738-21-2 N,9α-dibenzyl-trans-8-azabicyclo<4.3.0>non-4-en-7-one 
• 85738-21-2 N,9β-dibenzyl-trans-8-azabicyclo<4.3.0>non-4-en-7-one 
• 85738-21-2 N,9β-dibenzyl-cis-8-azabicyclo<4.3.0>non-4-en-7-one 
• 85738-13-2 (E)-Penta-2,4-dienoic acid benzyl-(1-benzyl-allyl)-amide 
• 66050-07-5 (1RS, 6SR, 9RS)-N,9-dibenzyl-cis-8-azabicyclo<4.3.0>nonan-7-one 
• 66050-07-5 (1RS, 6RS, 9RS)-N,9-dibenzyl-8-azabicyclo<4.3.0>nonan-7-one 
• 66050-07-5 (1RS, 6RS, 9SR)-N,9-dibenzyl-8-azabicyclo<4.3.0>nonan-7-one 
• 66050-07-5 (1RS, 6SR, 9SR)-N,9-dibenzyl-8-azabicyclo<4.3.0>nonan-7-one 
• 85738-08-5 N-(1-benzylprop-2-enyl)benzylamine 
• 6431-57-8 1-Ethynylphenethylamin 

Relevant academic research and scientific papers

Catalytic Nucleophilic Fluorination of Secondary and Tertiary Propargylic Electrophiles with a Copper-N-Heterocyclic Carbene Complex

A catalytic method for the nucleophilic fluorination of propargylic electrophiles is described. Our protocol involves the use of a Cu(NHC) complex as the catalyst and is suitable for the preparation of secondary and tertiary propargylic fluorides without

The Synthesis of 9-Substituted N-Benzyl-8-azabicyclonon-4-en-7-ones by the Intramolecular Diels-Alder Reaction

The intramolecular thermal cyclisation of N-allyl-N-benzylpenta-2(E),4-dienamide in refluxing NN-dimethylformamide gives N-benzyl-cis- and trans-8-azabicyclonon-4-en-7-one; N-allyl-N-benzylhexa-2(E),4(E)-dienamide gives (1RS, 3RS, 6SR)-3-methyl- an