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Synthesis of Pyridine-Fused Ring Systems from β-Chloroacroleins: A Comparison of Three Different Pathways.

✍ Scribed by Stephanie Hesse; Gilbert Kirsch

Book ID
101949477
Publisher
John Wiley and Sons
Year
2003
Weight
152 KB
Volume
34
Category
Article
ISSN
0931-7597

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✦ Synopsis

Abstract

For Abstract see ChemInform Abstract in Full Text.

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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 👁 1 views

## 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.
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## 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.