𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The tandem Diels-Alder reaction of dimethyl acetylenedicarboxylate to bicyclopentadiene. A theoretical study of the molecular mechanisms

✍ Scribed by Luis R. Domingo; Manuel Arnó; Juan Andrés

Publisher
Elsevier Science
Year
1996
Tongue
French
Weight
174 KB
Volume
37
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Alternative Mechanistic Paths in the Het
Alternative Mechanistic Paths in the Hetero-Diels–Alder Reaction of α-Oxothiones: A Theoretical Study
✍ Laura Legnani; Carlotta Lunghi; Franca Marinone Albini; Cristina Nativi; Barbara 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 177 KB

## Abstract DFT calculations at the B3LYP/6‐311+G(d,p) level for the C, H, and O atoms and at the 6‐311+G(2df,p) level for the S atom were used to study the hetero‐Diels–Alder reactions between several α‐oxothiones and ethylene or methyl vinyl ether (MVE). All the transition states and the intermed

Towards an Understanding of the Polar Di
Towards an Understanding of the Polar Diels–Alder Reactions of Nitrosoalkenes with Enamines: A Theoretical Study
✍ Luis R. Domingo; M. Teresa Picher; Pau Arroyo 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 212 KB 👁 1 views

## Abstract The polar Diels–Alder reactions of nitrosoalkenes with enamines have been studied using DFT methods at the B3LYP/6‐31G\* level of theory. These Diels–Alder reactions are characterized by a nucleophilic attack of the enamine at the conjugated position of the nitrosoalkene with concomitan