130834-34-3Relevant academic research and scientific papers
Conjugate addition of radicals generated from diacyloxyiodobenzenes to dehydroamino acid derivatives; a synthesis of diaminopimelic acid analogues
Sutherland, Andrew,Vederas, John C.
, p. 224 - 225 (2002)
Radical decomposition of bis((2S)-N-benzyloxycarbonyl-2-aminopentan-5-carboxy-1-methyl ester)iodobenzene followed by decarboxylation and subsequent conjugate addition with a series of selectively protected dehydroamino acids leads to new analogues of diam
Diastereoselective Radical Addition to Derivatives of Dehydroalanine and of Dehydrolactic Acid
Beckwith, Athelstan L. J.,Chai, Christina L. L.
, p. 1087 - 1088 (2007/10/02)
The cyclic methylene compounds (1)-(3) undergo diastereoselective free radical addition when treated with alkylmercury hydride or alkyl iodide/tributylstannane to give products useful for the enantioselective synthesis of α-amino and α-hydroxy acids.
