169774-81-6Relevant articles and documents
Towards a versatile synthesis of kainoids II: Two methods for establishment of C-4 stereochemistry
Baldwin, Jack E.,Bamford, Samantha J.,Fryer, Andrew M.,Rudolph, Martin P. W.,Wood, Mark E.
, p. 5255 - 5272 (2007/10/03)
Benzylic lactone hydrogenolysis and enamide reduction were used to generate protected C-4 aryl substituted kainoid analogues which were deprotected to their corresponding free amino acids. X-ray crystographic data were obtained for the C-4 2-MeOPh- analogue.
A versatile approach to acromelic acid analogues
Baldwin, Jack E.
, p. 4869 - 4872 (2007/10/02)
A route to acromelic acid analogues and their corresponding C-4 epimers from trans-4-hydroxy-L-proline is described. The C-4 substituent was introduced by a Suzuki-type boronate coupling to a vinyl triflate.