In order to develop a general synthesis of ADDA containing peptides, an asymmetric synthesis of the p-lactam 4 and initial investigations into its opening with aminoesters is described.
ChemInform Abstract: Towards an Asymmetric Synthesis of ADDA Conjugates.
β Scribed by D. J. CUNDY; A. C. DONOHUE; T. D. MCCARTHY
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Towards an Asymmetric Synthesis of ADDA Conjugates. -In order to develop a general synthesis of ADDA-containing peptides the synthesis of lactam (VII) via a optimized coupling of the aldehyde (II) with the sulfone (III) is detailed. Furthermore, initial investigations concerning ring opening of (VII) with the aminoester (VIII) are described. -(CUNDY, D.
π SIMILAR VOLUMES
An Asymmetric Synthesis of ADDA and ADDA-Glycine Dipeptide Using the Ξ²-Lactam Synthon Method. -The paper describes the use of lactam (X) in the synthesis of dipeptides such as (XIV). -(CUNDY,
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An Asymmetric Synthesis (-)-Epibatidine. -The title compound (X) is synthesized with a view to its biological activity and its low natural abundance. Key steps in this synthesis are the Pd-catalyzed desymmetrization of the dibenzoate (I) and the Pd-catalyzed cross coupling of the vinyl bromide (V)