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Volumn 48, Issue 6, 2007, Pages 967-969

A new procedure for the synthesis of peptide-derived Amadori products on a solid support

Author keywords

Amadori rearrangement; Glycation; Solid phase peptide synthesis

Indexed keywords

2,3:4,5 DI O ISOPROPYLIDENE BETA DEXTRO ARABINO HEXOS 2 ULO 2,6 PYRANOSE; CHEMICAL COMPOUND; UNCLASSIFIED DRUG;

EID: 33846082445     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.12.022     Document Type: Article
Times cited : (22)

References (14)
  • 11
    • 33846088184 scopus 로고    scopus 로고
    • note
    • Procedure for solid phase glycation: after deprotection (1% TFA in DCM; 10 min, rt, 7×) of the ε-amino group of lysine, the resin (470 mg) was suspended in 17 ml of a 1% solution of acetic acid in DMF. Then a twofold molar excess of 1 in 1 ml of DMF and a fivefold molar excess of sodium cyanoborohydride (with respect to loading of the resin) in 1 ml of DMF were added and the resin was agitated for 2 h at rt. The final reaction product was cleaved from the resin using TFA containing 5% water and 5% of TIS for 24 h at rt.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.