Synthesis of densely functionalized pyrrolidinone templates by an intramolecular oxo-Diels-Alder reaction was written by Murray, William V.;Mishra, Pranab K.;Sun, Sengen;Maden, Amy. And the article was included in Tetrahedron Letters in 2002.Related Products of 87694-53-9 This article mentions the following:
Preparation of densely functionalized pyrrolidinone templates, is a challenge for synthetic chemists. These templates are important building blocks for novel conformationally constrained natural products or for library generation of highly functionalized bi or polycyclic compounds Trienes, e.g. I, undergo facile stereoselective intramol. Diels Alder reactions to generate densely functionalized cis fused pyrrolidinone templates, e.g. II. These reactions allow for directed remote hydroxylation with complete control of stereochem. In the experiment, the researchers used many compounds, for example, (S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate (cas: 87694-53-9Related Products of 87694-53-9).
(S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate (cas: 87694-53-9) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Related Products of 87694-53-9
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics