## 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.
One-pot Regioselective Synthesis of Novel 1- N -Methyl-spiro[2,3′]oxindole-spiro[3,3″]-1″- N -arylpyrrolidine-2″,5″-dione-4-arylpyrrolidines through Multicomponent 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylide
✍ Scribed by Kaur, Anjandeep; Kaur, Manpreet; Singh, Baldev
- Book ID
- 121882739
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2014
- Tongue
- English
- Weight
- 627 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0022-152X
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## Abstract magnified image 2‐Arylidene‐1,3‐indanediones undergo a regioselective 1,3‐dipolar cycloaddition reaction with the azomethine ylide derived from isatin and sarcosine by decarboxylative route affording a series of 1‐N‐methyl — spiro[2.3′“]oxindole‐spiro[3.2”]indane‐1“,3”‐diones‐4‐aryl py
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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