Monodisperse oligo(para-phenyleneethynylene)s (oligo-protective groups for the acetylene moieties. The polar HOM group shows a strong impact on the chromatographic PPEs) were synthesized by a divergent-convergent synthesis starting behaviour of the products and makes the isolation of pure compounds
Hydrazinolysis of Dde: Complete orthogonality with Aloc protecting groups
β Scribed by Barbara Rohwedder; Yvan Mutti; Pascal Dumy; Manfred Mutter
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 199 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Hydrazinolysis of Dde group is troublesome in the presence of Aloc protected peptides. We elucidate that reduction of the Aloc double bond occurs both in solution and on solid support preventing the subsequent Aloc deprotection and resulting in mixtures difficult to purify. We report here that addition of allyl alcohol as scavenger circumvents this side reaction and provides a complete orthogonality between Dde and Aloc in solution and solid phase peptide synthesis.
π SIMILAR VOLUMES
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The synthesis of first-and second-generation dendrons with defined ratios of orthogonally protected amine groups in the periphery ((benzyloxy)carbonyl (Cbz) and (tert-butoxy)carbonyl (Boc) protection) and the degree to which they can be selectively removed are described. The reaction conditions requ