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In Search of New Approaches to Asymmetric Conjugate Addition: Screening Studies on the Use of [Zn(bpy*)X(R)] Reagents and α,β-Unsaturated Amide Michael Acceptors
Alexander J. Blake, Daniela Giunta, Jonathan Shannon, Maurizio Solinas, Francesca Walzer and Simon Woodward*
School of Chemistry, The University of Nottingham, University Park, Nottingham NG7 2RD, United Kingdom
Crossref Cited-by Linking
- Chen Guan-Jhen, Zeng Shi-Xian, Lee Cheng-Hsun, Chang Yu-Lun, Chang Chun-Juei, Ding Shangwu, Chen Hsuan-Ying, Wu Kuo-Hui, Chang I-Jy: Synthesis of zinc complexes bearing pyridine derivatives and their application of ε-caprolactone and L-Lactide polymerization. Polymer 2020, 194, 122374. <https://doi.org/10.1016/j.polymer.2020.122374>
- Allenbaugh Rachel J., Zachary Jonathon R., Williams Joseph R., Shaw Angela L., Bryson Jeffrey D., Underwood A. Nicole, O'Donnell Erin E.: Mechanochemical synthesis of zinc and palladium complexes of dialkyl 2,2′-bipyridine-4,4′-dicarboxylate and analysis of solid-state reaction kinetics. Inorganica Chimica Acta 2018, 477, 102. <https://doi.org/10.1016/j.ica.2018.03.004>
- Anderson James C., Campbell Ian B., Campos Sebastien, Shannon Jonathan, Tocher Derek A.: Stereoselective synthesis of 1,2-diamine containing indolines by a conjugate addition nitro-mannich reaction. Org. Biomol. Chem. 2015, 13, 170. <https://doi.org/10.1039/C4OB01793E>
- Esmhosseini Majid: (2,2′-Bipyridine-κ2N,N′)dibromido(dimethyl sulfoxide-κO)zinc(II). Acta Crystallogr E Struct Rep Online 2010, 66, m677. <https://doi.org/10.1107/S1600536810017551>
- Blake Alexander J., Giunta Daniela, Shannon Jonathan, Solinas Maurizio, Walzer Francesca, Woodward Simon: ChemInform Abstract: In Search of New Approaches to Asymmetric Conjugate Addition: Screening Studies on the Use of [Zn(bpy*)X(R)] Reagents and α,β‐Unsaturated Amide Michael Acceptors. ChemInform 2008, 39. <https://doi.org/10.1002/chin.200802048>
- Biswas Kallolmay, Woodward Simon: Stereoselective 1,4-addition of Grignard reagents to α,β-enamides using a combined chiral auxiliary-catalyst approach. Tet Asymm 2008, 19, 1702. <https://doi.org/10.1016/j.tetasy.2008.06.017>
