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.

 
  • References

  • 1 Merrifield RB. J. Am. Chem. Soc. 1963; 85: 2149
    • 2a Lam KS, Salmon SE, Hersh EM, Hruby VJ, Kazmierski WM, Knapp RJ. Nature (London) 1991; 354: 82
    • 2b Kim YG, Shin DS, Kim EM, Park HY, Lee CS, Kim JH, Lee BS, Lee YS, Kim BG. Angew. Chem. Int. Ed. 2007; 119: 5408
    • 2c Shin DS, Kim YG, Kim EM, Kim M, Park HY, Kim JH, Lee BS, Kim BG, Lee YS. J. Comb. Chem. 2008; 10: 20
    • 3a Rink H. Tetrahedron Lett. 1987; 28: 3787
    • 3b Atherton E, Logan CJ, Sheppard RC. J. Chem. Soc., Perkin Trans. 1 1981; 538
    • 3c Kenner GW, McDermott JR, Sheppard RC. J. Chem. Soc., Chem. Commun. 1971; 636
    • 4a Holmes CP, Jones DG. J. Org. Chem. 1995; 60: 2318
    • 4b Brown BB, Wagner DS, Geysen HM. Mol. Diversity 1995; 1: 4
  • 5 Tan C, Weaver D. Tetrahedron 2002; 58: 7449
  • 6 Kim H, Cho JK, Chung WJ, Lee YS. Org. Lett. 2004; 6: 3273
  • 7 Cho JK, Park BD, Lee YS. Tetrahedron Lett. 2000; 41: 7481