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Synthesis of some monocyclic analogues of mycophenolic acid via the Johnson ortho ester Claisen rearrangement by Ma Elena Meza-Aviña; Mario Ordoñez; Mario Fernández-Zertuche; Lourdes Rodríguez-Fragoso; Jorge Reyes-Esparza; Abril A. Martínez de los Ríos-Corsino is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
What is Synthesis of some monocyclic analogues of mycophenolic acid via the Johnson ortho ester Claisen rearrangement about?
The synthesis of some monocyclic analogues of mycophenolic acid in which the lactone ring has been eliminated, leaving the aromatic ring intact and the same oxygenated substituents flanking the hexenoic acid side chain with an (E)-geometry at the double bond, has been accomplished via the Johnson ortho ester Claisen rearrangement. The synthetic methodology reported here allows the preparation of mycophenolic acid analogues bearing alkyl substituents at the a-and b-positions on the side chain.
Who reads Synthesis of some monocyclic analogues of mycophenolic acid via the Johnson ortho ester Claisen rearrangement?
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- Ma Elena Meza-Aviña; Mario Ordoñez; Mario Fernández-Zertuche; Lourdes Rodríguez-Fragoso; Jorge Reyes-Esparza; Abril A. Martínez de los Ríos-Corsino
- Publisher
- Elsevier Science; Elsevier ; Elsevier Ltd.; Elsevier BV (ISSN 0968-0896)
- Published
- 2005
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)