𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Efficient Pyrrole Synthesis Using Double Nucleophilic Addition to α,β-Unsaturated Imines with Plural Nucleophiles.

✍ Scribed by Makoto Shimizu; Atsushi Takahashi; Shiho Kawai


Publisher
John Wiley and Sons
Year
2006
Weight
42 KB
Volume
37
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


A New Method for the Synthesis of Multis
✍ Atsushi Takahashi; Shiho Kawai; Iwao Hachiya; Makoto Shimizu 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 270 KB

## Abstract Double nucleophilic addition reactions of dialkoxy ketenesilyl acetals proceeded with α,β‐unsaturated imines to give 1,4‐ and 1,2‐double addition products, and their subsequent transformations afforded multisubstituted pyrroles in good yields. Application of this procedure to the synthe

An Efficient Synthesis of Achiral and Ch
✍ Francisco Palacios; Javier Vicario; Domitila Aparicio 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 25 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

An Efficient Synthesis of Achiral and Ch
✍ Francisco Palacios; Javier Vicario; Domitila Aparicio 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 156 KB

## Abstract A very simple and efficient synthesis of 3‐amino‐1,5‐dihydro‐2__H__‐pyrrol‐2‐ones is reported. These cyclic dehydro‐amino acid derivatives with a stereogenic center at the 5‐position were obtained by the addition of two equivalents of amine to β,γ‐unsaturated keto esters. These cyclic e