An efficient multicomponent and stereoselective synthesis of new spiro[indeno[1,2-b]quinoxaline-11,2′-pyrrolidine] derivatives
✍ Scribed by Mehdi Moemeni; Hamid Arvinnezhad; Saadi Samadi; Mahmood Tajbakhsh; Khosrow Jadidi; Hamid Reza Khavasi
- Book ID
- 102344213
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2011
- Tongue
- English
- Weight
- 277 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.685
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✦ Synopsis
Abstract
New spiro[indeno[1,2‐b]quinoxaline‐11,2′‐pyrrolidine] derivatives were prepared in high yield stereoselectively from an efficient multicomponent 1,3‐dipolar cycloaddition reaction between ninhydrin, phenylenediamine, sarcosine, and chalcones. The regiochemistry and stereochemistry of resultant cycloadducts have been determined by several 2D NMR spectroscopic techniques and X‐ray single crystal diffraction. J. Heterocyclic Chem., (2012).
📜 SIMILAR VOLUMES
Simple and improved conditions have been found for the synthesis of 3-pyrrolyl-indolinones and pyrrolyl-indeno[1,2-b]quinoxalines by coupling of 4-hydroxyproline with isatins and 11H-indeno[1,2-b]quinoxalin-11-ones using Keggin (H 3 PW 12 O 40 ) and Well-Dawson tungsten heteropolyacids (H 6 P 2 W 18