## Abstract Intermolecular tandem‐Michael/Michael addition reactions of alkyne acceptors and CH‐acidic compounds such as 1,3‐cyclohexanedione (**2a**) and dimedone (**2b**) under L‐proline catalysis furnished four new products **1a**–**d** with __C__~2~ axial chirality. (© Wiley‐VCH Verlag GmbH & C
Synthesis and Characterization of Hyperbranched Poly(β-ketoester) by the Michael Addition
✍ Scribed by Yang-Bae Kim; Hyun Kyoung Kim; Haruo Nishida; Takeshi Endo
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 95 KB
- Volume
- 289
- Category
- Article
- ISSN
- 1438-7492
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✦ Synopsis
Abstract
Summary: A novel hyperbranched poly(β‐ketoester) was synthesized from 2‐(acetoacetoxy)ethyl acrylate by the Michael addition in the presence of 1,8‐diazabicyclo[5.4.0]undec‐7‐ene (DBU) as catalyst. ^1^H NMR integration experiments revealed that the degree of branching in the poly(β‐ketoester) was remarkably high at a level of 82.9%. The number‐average molecular weight of the polymer was between 2 100 and 12 000 and increased with reaction temperature and conversion.
Synthesis of hyperbranched polymer by Michael addition of AAEA.
magnified imageSynthesis of hyperbranched polymer by Michael addition of AAEA.
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## 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 of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## 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