121129-41-7Relevant academic research and scientific papers
Asymmetric Induction in the Diels-Alder Reactions of α-Hydroxy Acyl Nitrones
Kirby, Gordon W.,Nazeer, Muhammad
, p. 1397 - 1402 (2007/10/02)
The hydroxamic acids 7, derived from a series of α-hydroxy acids 5, have been oxidised with periodate to form transient, chiral acyl nitroso compounds 8, which were trapped in situ with cyclopentadiene and cyclohex-1,3-diene to give mixtures of diastereoi
ASYMMETRIC INDUCTION IN THE DIELS-ALDER REACTIONS OF α-HYDROXYACYLNITROSO COMPOUNDS
Kirby, Gordon W.,Nazeer, Muhammad
, p. 6173 - 6174 (2007/10/02)
Transient, chiral α-hydroxyacylnitroso compounds (2), able to form intramolecular hydrogen bonds, react stereoselectively with cyclopentadiene and cyclohexa-1,3-diene; the cycloadduct (6) of the latter diene and the nitroso derivative of (S)-mandelic acid
