𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A Facile Synthesis of a New Class of Eight-Membered Heterocycles from 1-Azabutadienes

✍ Scribed by Prof. Dr. José Barluenga; Dr. Miguel Tomás; Alfredo Ballesteros; Prof. Dr. Vicente Gotor; Prof. Dr. Carl Krüger; Yi-Hung Tsay

Publisher
John Wiley and Sons
Year
1986
Tongue
English
Weight
243 KB
Volume
25
Category
Article
ISSN
0044-8249

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of some new five membered hete
Synthesis of some new five membered heterocycles, a facile synthesis of oxazolidinones
✍ Ahmet Demirbas; Sule Ceylan; Neslihan Demirbas 📂 Article 📅 2007 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 558 KB

## Abstract magnified image The synthesis and structural properties of two kinds of thiosemicarbazide derivatives (**2a‐c** and **3a‐c**) and one kind of semicarbazide derivatives (**4a, 4b**) have been described. These compounds were synthesized by treating 2‐(4‐amino‐3‐alkyl‐5‐oxo‐4,5‐dihydro‐1_

ChemInform Abstract: Synthesis of Some N
ChemInform Abstract: Synthesis of Some New Five Membered Heterocycles. A Facile Synthesis of Oxazolidinones.
✍ Ahmet Dermirbas; Sule Ceylan; Neslihan Demirbas 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 43 KB 👁 1 views

## 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 of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Synthesis of a new class of spiro hetero
Synthesis of a new class of spiro heterocycles
✍ Venkatapuram Padmavathi; Kaveti Sudheer; Dandu Rangayapalle Chinna Venkata Subba 📂 Article 📅 2008 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 346 KB 👁 1 views

## Abstract magnified image A new class of spiro heterocycles __viz__., spiropyrazolidinediones, isoxazolidinediones, pyrimidinetriones or thioxopyrimidinediones are developed from methyl 3‐aryl‐2‐(__Z__‐arylethenenylsulfonyl)acrylate by double Michael addition reaction with dimethyl malonate foll