A facile and efficient stereoselective synthesis of highly functionalised trisubstituted alkene derivatives of ferrocenealdehyde
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference41 articles.
1. Use of Weakly Coordinating Anions to Develop an Integrated Approach to the Tuning of ΔE1/2 Values by Medium Effects
2. The syntheses and catalytic applications of unsymmetrical ferrocene ligands
3. Structures and Electrocommunication between Ferrocenyl Groups in Osmium Cluster Complexes of 1,8-Bis(ferrocenyl)octatetrayne
4. Structures and Electrocommunication between Ferrocenyl Groups in Osmium Cluster Complexes of 1,8-Bis(ferrocenyl)octatetrayne
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1. Biphenyl 3- and 4- mono and 4, 4′-dicarbaldehyde as Electrophiles and Unusual Michael Acceptors in the Baylis-Hillman Reaction: Synthesis of Functionalized Biphenyl Derivatives;ChemistrySelect;2018-11-02
2. Bipyridine carbaldehydes as electrophiles in the Morita–Baylis–Hillman reaction: synthesis of highly functionalized bipyridyl ligands and a macrocycle;Tetrahedron Letters;2015-10
3. Development of a mild and efficient protocol for the protection and O-alkylation of allyl alcohols;RSC Adv.;2014
4. Synthesis of novel ferrocenyl N/O-heterocycles, chiral P,N-ligand and α-dehydro-β-amino acid derived short peptides from Morita–Baylis–Hillman adducts of ferrocenealdehyde;RSC Adv.;2014
5. An efficient copper catalyzed one-pot, four-component, and diastereoselective synthesis of highly functionalized ferrocenyl azetidinimines;Tetrahedron Letters;2013-06
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