p??Nitrobenzyloxycarbonyl (pNZ) as a Temporary Nα??Protecting Group in Orthogonal Solid??Phase Peptide Synthesis–Avoiding Diketopiperazine and Aspartimide …
A Isidro??Llobet, J Guasch??Camell…
Index: Isidro-Llobet, Albert; Guasch-Camell, Judit; Alvarez, Mercedes; Albericio, Fernando European Journal of Organic Chemistry, 2005 , # 14 p. 3031 - 3039
Full Text: HTML
Citation Number: 22
Abstract
Abstract p-Nitrobenzyloxycarbonyl (pNZ) was used as a temporary protecting group for α- amino functionalities in solid-phase peptide synthesis. The corresponding derivatives are readily synthesized solids that perform well on solid phase. The pNZ moiety is orthogonal with the most common protecting groups used in peptide chemistry, and is removed under neutral conditions in the presence of catalytic amounts of acid. The use of pNZ derivatives ...
Related Articles:
[Carpenter; Gish Journal of the American Chemical Society, 1952 , vol. 74, p. 3818,3819]
[Carpenter; Gish Journal of the American Chemical Society, 1952 , vol. 74, p. 3818,3819]
[Blaha,K.; Rudinger,J. Collection of Czechoslovak Chemical Communications, 1965 , vol. 30, p. 585 - 598]