𝔖 Bobbio Scriptorium
✦   LIBER   ✦

One-Pot Synthesis of Dispiro[oxindole-3,3′-pyrrolidines] by Three-Component [3+2] Cycloadditions of in situ -Generated Azomethine Ylides with 3-Benzylidene-2,3-dihydro-1 H -indol-2-ones

✍ Scribed by Matloubi Moghaddam, Firouz; Kiamehr, Mostafa; Reza Khodabakhshi, Mohammad; Jebeli Javan, Marjan; Fathi, Shaghayegh; Villinger, Alexander; Iaroshenko, Viktor O.; Langer, Peter

Book ID
121656258
Publisher
John Wiley and Sons
Year
2013
Tongue
German
Weight
393 KB
Volume
96
Category
Article
ISSN
0018-019X

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

One pot synthesis of novel dispiro[oxind
One pot synthesis of novel dispiro[oxindole-thiazolidinedione/thioxo-thiazolidinone/dihydro pyrazolone]-pyrrolidines via 1,3-dipolar cycloaddition reaction of azomethine ylides
✍ Shashikanth Ponnala; Devi Prasad Sahu; Rishi Kumar; Prakas R. Maulik 📂 Article 📅 2006 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 560 KB

## Abstract magnified image A series of novel dispiro[oxindole‐thiazolidinedione]pyrrolidine, dispiro[oxindole‐thioxothiazolidinone]‐pyrrolidine, dispiro[oxindole‐dihydro‐pyrazolone]pyrrolidine were synthesized by both regio‐ and stereo‐selective 1,3‐dipolar cycloaddition reaction of azomethine yl

On the Reactions of Furan-2,3-diones wit
On the Reactions of Furan-2,3-diones with Oxindole (=1,3-Dihydro-2H-indol-2-one) and Lawesson Reagent. Synthesis of New 1,3-Dihydro-2H-indol-2-ones, Bis-furanones, and Bis-pyrrolones
✍ Elif Korkusuz; İsmail Yıldırım 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 German ⚖ 235 KB

## Abstract Lactone analogues of 3‐substituted oxindoles (=1,3‐dihydro‐2__H__‐indol‐2‐ones) and nonbenzoid oxa‐analogous isoindigoid or nonbenzoid isoindigoid dyes were prepared by the reactions of furan‐2,3‐diones with oxindole and __Lawesson__ reagent (__Schemes 1__ and __3__), respectively. So,