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ChemInform Abstract: Highly Stereoselective Synthesis of Spiropyrazolones.

โœ Scribed by Andrea-Nekane R. Alba; Alex Zea; Guillem Valero; Teresa Calbet; Merce Font-Bardia; Andrea Mazzanti; Albert Moyano; Ramon Rios

Publisher
John Wiley and Sons
Year
2011
Weight
31 KB
Volume
42
Category
Article
ISSN
0931-7597

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โœฆ Synopsis

Abstract

The title compounds are obtained through a Michaelโ€”Michaelโ€aldol reaction in good yields and with high diastereoโ€ and enantioselectivity.

๐Ÿ“œ SIMILAR VOLUMES

Highly Stereoselective Synthesis of Spir
Highly Stereoselective Synthesis of Spiropyrazolones
โœ Andrea-Nekane R. Alba; Alex Zea; Guillem Valero; Teresa Calbet; Merce Font-Bardรญ ๐Ÿ“‚ Article ๐Ÿ“… 2011 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 648 KB

## Abstract The synthesis of spiro compounds through a Michaelโ€“Michaelโ€“aldol reaction is reported. The reaction affords spiropyrazolone derivatives in good yields, in almost diastereoโ€ and enantiopure form, and is catalyzed by diphenylprolinol derivatives. The reaction showed strong nonlinear effec

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## 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 โ€œFull Textโ€ option. The original article is trackable v