296774-86-2Relevant academic research and scientific papers
Scope and limitations in the use of N-(PhF)serine-derived cyclic sulfamidates for amino acid synthesis
Wei,Lubell
, p. 94 - 104 (2007/10/03)
Ring-opening of N-(PhF)serine-derived cyclic sulfamidate 17 was achieved with different nucleophiles (βketo esters, β-keto ketones, dimethyl malonate, nitroethane, sodium azide, imidazole, and potassium thiocyanate) to prepare a variety of amino acid anal
Racemization in the use of N-(9-(9-phenylfluorenyl))serine-derived cyclic sulfamidates in the synthesis of delta-keto alpha-amino carboxylates and prolines.
Wei,Lubell
, p. 2595 - 2598 (2007/10/03)
[reaction: see text]Ring opening of enantiopure N-(9-(9-phenylfluorenyl)serine-derived cyclic sulfamidates with beta-keto esters, beta-keto ketones, and dimethyl malonate gave a variety of gamma-substituted amino acid analogues in racemic form. Investigat
