160024-73-7Relevant academic research and scientific papers
Enantiospecific synthesis of 3-pyrrolines: A route to novel polyhydroxylated pyrrolidines
Burley, Ian,Hewson, Alan T.
, p. 7099 - 7102 (1994)
Enantiomer acetamido ketones are converted by an intramolecular Wittig reaction into enantiopure 3-pyrrolines; the product from (S)-serine provides access to novel polyhydroxylated pyrrolidines.
Allylboration of α-Amino Ketones
Pace, R. David,Kabalka, George W.
, p. 4838 - 4844 (2007/10/02)
A series of unsaturated α-amino alcohols were prepared via the allylboration of the corresponding N-protected α-amino ketones.The reactions are stereoselective, producing the syn isomers.The diastereoselectivity is not dramatically affected by the electro
