Synlett 2013; 24(6): 733-736
DOI: 10.1055/s-0032-1318314
letter
© Georg Thieme Verlag Stuttgart · New York

Facile Synthesis of N-(9-Fluorenylmethyloxycarbonyl)-3-amino-3-(4,5-dimethoxy-2-nitrophenyl)propionic Acid as a Photocleavable Linker for Solid-Phase Peptide Synthesis

Jaehi Kim*
School of Chemical and Biological Engineering, Seoul National University, Gwanak-Gu, Seoul 151-744, Korea   Fax: +82(2)8769625   Email: yslee@snu.ac.kr
,
San Kyeong
School of Chemical and Biological Engineering, Seoul National University, Gwanak-Gu, Seoul 151-744, Korea   Fax: +82(2)8769625   Email: yslee@snu.ac.kr
,
Dong-Sik Shin
School of Chemical and Biological Engineering, Seoul National University, Gwanak-Gu, Seoul 151-744, Korea   Fax: +82(2)8769625   Email: yslee@snu.ac.kr
,
Sewon Yeo
School of Chemical and Biological Engineering, Seoul National University, Gwanak-Gu, Seoul 151-744, Korea   Fax: +82(2)8769625   Email: yslee@snu.ac.kr
,
Joonhyuk Yim
School of Chemical and Biological Engineering, Seoul National University, Gwanak-Gu, Seoul 151-744, Korea   Fax: +82(2)8769625   Email: yslee@snu.ac.kr
,
Yoon-Sik Lee
School of Chemical and Biological Engineering, Seoul National University, Gwanak-Gu, Seoul 151-744, Korea   Fax: +82(2)8769625   Email: yslee@snu.ac.kr
› Author Affiliations
Further Information

Publication History

Received: 26 December 2012

Accepted after revision: 05 February 2013

Publication Date:
04 March 2013 (online)


Abstract

A photocleavable linker, N-(9-fluorenylmethyloxycarbonyl)-3-amino-3-(4,5-dimethoxy-2-nitrophenyl)propionic acid was synthesized from veratraldehyde, with simple reaction and separation steps. This linker was stable under the normal solid-phase peptide synthesis conditions and rearranged to a labile form when irradiated with UV light (λ = 365 nm). A model peptide sequence (YGGFL) was synthesized and released from solid supports with high efficiency by UV irradiation.