Cyanoacetamide-based oxime carbonates: An efficient, simple alternative for the introduction of Fmoc with minimal dipeptide formation

Tetrahedron

Volumn 68, Issue 14, 2012, Pages 3056-3062

  Khattab, Sherine N ^a,b   Subirós Funosas, Ramon ^b,c   El Faham, Ayman ^a,b   Albericio, Fernando ^b,c,d  

^a Alexandria University Faculty Of Science   (Egypt)

^b INSTITUTE FOR RESEARCH IN BIOMEDICINE   (Spain)

^c UNIVERSITY OF BARCELONA   (Spain)

^d UNIVERSITY OF KWAZULU NATAL   (South Africa)

Author keywords

9 Fluorenylmethyloxycarbonyl; Amino acids; N Protecting group; Oxime; Peptide synthesis

Indexed keywords

2 (ETHYLAMINO) N HYDROXY 2 OXOACETIMIDOYL CYANIDE; 2 AMINO N HYDROXY 2 OXOACETIMIDOYL CYANIDE; ACETAMIDE DERIVATIVE; CARBONIC ACID DERIVATIVE; CARBONYL DERIVATIVE; CYANOACETAMIDE; DIPEPTIDE; FLUORENYLMETHYLOXYCARBONYL; N [[(9H FLUOREN 9 YL)METHOXY]CARBONYLOXY] 2 (ETHYLAMINO) 2 OXOACETIMIDOYL CYANIDE; N [[(9H FLUOREN 9 YL)METHOXY]CARBONYLOXY] 2 AMINO 2 OXOACETIMIDOYL CYANIDE; N [[(9H FLUOREN 9 YL)METHOXY]CARBONYLOXY] 2 MORPHOLINO 2 OXOACETIMIDOYL CYANIDE; N [[(9H FLUOREN 9 YL)METHOXY]CARBONYLOXY] 2 OXO 2 (PIPERIDIN 1 YL)ACETIMIDOYL CYANIDE; N HYDROXY 2 MORPHOLINO 2 OXOACETIMIDOYL CYANIDE; N HYDROXY 2 OXO 2 (PIPERIDIN 1 YL)ACETIMIDOYL CYANIDE; OXIME DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; PRIORITY JOURNAL;

EID: 84858709753     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.02.020     Document Type: Article

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