𝔖 Bobbio Scriptorium
✦   LIBER   ✦

First Total Synthesis of (±)-Strychnofoline via a Highly Selective Ring-Expansion Reaction

✍ Scribed by Lerchner, Andreas; Carreira, Erick M.


Book ID
120670991
Publisher
American Chemical Society
Year
2002
Tongue
English
Weight
63 KB
Volume
124
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthesis of (±)-Strychnofoline via a Hi
✍ Andreas Lerchner; Erick M. Carreira 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 502 KB

## Abstract Studies aimed at preparing (±)‐strychnofoline by total synthesis are detailed. The route described makes use of a recently developed MgI~2~‐mediated ring‐expansion reaction of spiro[cyclopropan‐1,3′‐oxindole] with a cyclic disubstituted aldimine. The ring‐expansion product was formed as