Synthesis of nucleo aminooxy acid derivatives

Synthesis (Germany)

Volumn 45, Issue 1, 2013, Pages 134-140

  Noel, Olivier ^a   Xie, Juan ^a  

^a UNIVERSITÉ PARIS SACLAY   (France)

Author keywords

amides; cytosine; eliminations; l serine; N oxy nucleopeptides; nucleo aminooxy acids; nucleopeptides; thymine; triazoles

Indexed keywords

CYTOSINE; ELIMINATIONS; L -SERINE; NUCLEOPEPTIDES; THYMINE; TRIAZOLES;

AMIDES; AMINO ACIDS; NUCLEIC ACIDS;

PEPTIDES;

3 (AMINOOXY) 2 [2 [4 [[(BENZYLOXY)CARBONYL]AMINO] 2 OXOPYRIMIDIN 1 (2H) YL]ACETAMIDO]PROPANOIC ACID; 3 (AMINOOXY) 2 [2 [5 METHYL 2,4 DIOXO 3,4 DIHYDROPYRIMIDIN 1 (2H) YL]ACETAMIDO]PROPANOIC ACID; AMINOOXYACETIC ACID; BENZYL [2 OXO 1 (PROP 2 YM 1 YL) 1,2 DIHYDROPYRIMIDIN 4 YL]CARBAMIC ACID; CYTOSINE; METHYL 2 (2 [4 [(4 [[(BENZYLOXY)CARBONYL]AMINO] 2 OXOPYRIMIDIN 1 (2H) YL)METHYL] 1H 1,2,3 TRIAZOL 1 YL]ACETAMIDO) 3 [(1,3 DIOXOISOINDOLIN 2 YL)OXY]PROPANOIC ACID; METHYL 2 (2 AZIDOACETAMIDO) 3 [(1,3 DIOXOISOINDOLIN 2 YL)OXY]PROPANOIC ACID; METHYL 2 (2 AZIDOACETAMIDO)ACRYLIC ACID; METHYL 2 (2 CHLOROACETAMIDO) 3 [(1,3 DIOXOISOINDOLIN 2 YL)OXY]PROPANOIC ACID; METHYL 2 [2 (4 [[(BENZYLOXY)CARBONYL]AMINO] 2 OXOPYRIMIDIN 1 (2H) YL)ACETAMIDO] 3 [(1,3 DIOXOISOINDOLIN 2 YL)OXY]PROPANOIC ACID; METHYL 2 [2 (4 [[5 METHYL 2,4 DIOXO 3,4 DIHYDROPYRIMIDIN 1 (2H) YL]METHYL] 1H 1,2,3 TRIAZOL 1 YL)ACETAMIDO]ACRYLIC ACID; METHYL 2 [2 [4 [[(BENZYLOXY)CARBONYL]AMINO] 2 OXOPYRIMIDIN 1 (2H) YL]ACETAMIDO] 3 [[BIS(TERT BUTOXYCARBONYL)AMINO]OXY]PROPANOIC ACID; METHYL 2 [[(BENZYLOXY)CARBONYL]AMINO] 3 [[BIS(TERT BUTOXYCARBONYL)AMINO]OXY]PROPANOIC ACID; METHYL 3 [(1,3 DIOXOISOINDOLIN 2 YL)OXY] 2 [2 (4 [[5 METHYL 2,4 DIOXO 3,4 DIHYDROPYRIMIDIN 1 (2H) YL]METHYL] 1H 1,2,3 TRIAZOL 1 YL)ACETAMIDO]PROPANOIC ACID; METHYL 3 [[(TERT BUTOXYCARBONYL)AMINO]OXY] 2 [2 [5 METHYL 2,4 DIOXO 3,4 DIHYDROPYRIMIDIN 1 (2H) YL]ACETAMIDO]PROPANOIC ACID; METHYL 3 [[BIS(TERT BUTOXYCARBONYL)AMINO]OXY] 2 [2 [5 METHYL 2,4 DIOXO 3,4 DIHYDROPYRIMIDIN 1 (2H) YL]ACETAMIDO]PROPANOIC ACID; N TRITYL SERINE METHYL ESTER; O PHTHALIMIDO N TRITYL SERINE METHYL ESTER; O PHTHALIMIDO SERINE METHYL ESTER; THYMINE; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; ELECTROSPRAY MASS SPECTROMETRY; ELIMINATION REACTION; ENZYME DEGRADATION; HIGH RESOLUTION MELTING ANALYSIS; PROTEIN SECONDARY STRUCTURE; PROTEIN STABILITY; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 84871623073     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0032-1317689     Document Type: Article

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