188990-06-9Relevant academic research and scientific papers
A bromoarene based approach to phenylalanine analogues Hic and Nic
Gibson, Susan E.,Jones, Jerome O.,McCague, Ray,Tozer, Matthew J.,Whitcombe, Nicole J.
, p. 954 - 956 (2007/10/03)
A Heck reaction system incorporating Ph4PCl and using bromoarenes as substrates has enabled the syntheses of the conformationally constrained phenylalanine analogues Hic and Nic to be dramatically shortened thus facilitating the production of significant quantities of these amino acids.
Synthesis of conformationally constrained phenylalanine analogues via 7-, 8- and 9-endo Heck cyclisations
Gibson, Susan E.,Guillo, Nathalie,Middleton, Richard J.,Thuilliez, Audrey,Tozer, Matthew J.
, p. 447 - 455 (2007/10/03)
The novel conformationally constrained phenylalanine analogues 2,3,4,5-tetrahydro-1H-3-benzazepine-2-carboxylic acid (Sic) 1, 1,2,3,4,5,6-hexahydro-3-benzazocine-2-carboxylic acid (Hic) 2 and 2,3,4,5,6,7-hexahydro-1H-3-benzazonine-2-carboxylic acid (Nic)
