𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of a novel series of 10-oxa-3-aza-tricyclo[5.2.1.01,5]dec-8-en-4-ones through an intramolecular Diels–Alder reaction

✍ Scribed by Karen L. Milkiewicz; Irina B. Neagu; Daniel J. Parks; Tianbao Lu

Publisher
Elsevier Science
Year
2003
Tongue
French
Weight
126 KB
Volume
44
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis

The synthesis of a novel series of 10-oxa-3-aza-tricyclo[5.2.1.0 1,5 ]dec-8-en-4-ones through the use of the intramolecular Diels-Alder reaction is presented. The use of this reaction allows for the synthesis of functionalized polycyclic systems in a stereocontrolled manner.

📜 SIMILAR VOLUMES

Asymmetric synthesis of methyl N-(1-phen
Asymmetric synthesis of methyl N-(1-phenylethyl)-3-aza-10-oxatricyclo[5.2.1.01,5]-4-oxo dec-8-en-6-carboxylate by an intramolecular Diels-Alder reaction
✍ J Zylber; A Tubul; P Brun 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 184 KB

The title compound can be obtained with up to five asymmetric centres of known absolute configuration by a diastereoselective intramolecular Diels-Alder reaction between optically active N-substituted fuffurylamines and maleic anhydride, in which the chirality is transferred from one stereocentre to