𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Anionic Domino Process for the One-Pot, Diastereoselective Synthesis of Dihydropyranols from β-Nitroalcohols.

✍ Scribed by Roberto Ballini; Luciano Barboni; Dennis Fiorini; Alessandro Palmieri

Publisher
John Wiley and Sons
Year
2005
Weight
24 KB
Volume
36
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of Highly Substituted Cyclobut
Synthesis of Highly Substituted Cyclobutane Fused-Ring Systems from N-Vinyl β-Lactams through a One-Pot Domino Process
✍ Lawrence L. W. Cheung; Andrei K. Yudin 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 355 KB

## Abstract In this contribution, aminocyclobutanes, as well as eight‐membered enamide rings, have been made from __N__‐vinyl β‐lactams. The eight‐membered products have been formed by a [3,3]‐sigmatropic rearrangement, whereas the aminocyclobutanes have been derived from a domino [3,3]‐rearrangeme

ChemInform Abstract: Synthesis of Highly
ChemInform Abstract: Synthesis of Highly Substituted Cyclobutane Fused-Ring Systems from N-Vinyl β-Lactams Through a One-Pot Domino Process.
✍ Lawrence L. W. Cheung; Andrei K. Yudin 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 99 KB

## Abstract A domino [3.3]‐rearrangement/6π‐electrocyclization process furnishes highly substituted pyridine‐fused cyclobutane derivatives and thus provides an promising method for preparation of fused heterocycles.