𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Reactions of Glutaconic and Homophthalic Anhydrides with Imidates, Imidoyl Chlorides, and 1-Chloroisoquinoline

✍ Scribed by Stanoeva, Elena ;Haimova, Marietta ;Ognyanov, Vassil


Publisher
John Wiley and Sons
Year
1984
Tongue
English
Weight
303 KB
Volume
1984
Category
Article
ISSN
0947-3440

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Glutaconic anhydride (9) reacts with N‐substituted benzimidoyl chlorides 3 to give the corresponding (Z)‐3‐[(amino)(phenyl)methylene]pyrandiones 12, whereas with 1‐chloroisoquinoline (4) the benzo[a]quinolizinone 13 is obtained. The reactions of α‐methylhomophthalic anhydride (10) with 3 and the imidate 7 lead to the 1 (2__H__)‐isoquinolinones 14 and 19, respectively, and with 4 to the 13‐methyldibenzo[a,g]quinolizinone 15. The interaction of homophthalic anhydrides 1a, b with 3 aiming at the preparation of α‐condensation products is investigated.


📜 SIMILAR VOLUMES


Reactions of phosphoric anhydride with a
✍ Eva A. Oberlander; John C. Tebby 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 140 KB 👁 2 views

Acyclic secondary amides such as benzanilides 1a-g, acetanilides 2a-d, and benzamide 1h undergo selfcondensation in the presence of phosphoric anhydride to produce, in one step, N-substituted aroyl benzamidines 3a-g, acyl acetamidines 4a-d, and imide 5, respectively. Mechanistic evidence is presente

ChemInform Abstract: Reaction of Acyl Ch
✍ I. BOSCH; A. GONZALEZ; F. URPI; J. VILARRASA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

Reaction of Acyl Chlorides and Carboxylic Anhydrides with Phosphazenes. -The reaction of acyl chlorides or carboxylic acid anhydrides (I) and ( IV) with the phosphazenes (II) is systematically investigated. The distribution of the products (V) and (VI) depends on the solvent, temperature and reactio

Reactions of Imidoyl Isoselenocyanates w
✍ YuehuiDong Zhou; Anthony Linden; Heinz Heimgartner 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 German ⚖ 324 KB

## Abstract The reaction of __N__‐phenylimidoyl isoselenocyanates **1** with 2‐amino‐1,3‐thiazoles **10** in acetone proceeded smoothly at room temperature to give 4__H__‐1,3‐thiazolo[3,2‐__a__] [1,3,5]triazine‐4‐selones **13** in fair yields (__Scheme 2__). Under the same conditions, **1** and 2‐a