메뉴 건너뛰기




Volumn 31, Issue 3, 2006, Pages 337-339

Preparation of β-nitroalanine using the Easton three-component coupling method

Author keywords

Amino acid; Decarboxylation; Nitroalanine; Three component coupling

Indexed keywords

ACETIC ACID DERIVATIVE; ALANINE DERIVATIVE; ASPARTIC ACID DERIVATIVE; BETA NITROALANINE; BETA NITROASPARTATE; NITROACETIC ACID; NITROALKANE; NITROMETHANE; UNCLASSIFIED DRUG;

EID: 33749576769     PISSN: 09394451     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00726-006-0261-x     Document Type: Conference Paper
Times cited : (1)

References (14)
  • 1
    • 0019461464 scopus 로고
    • Inactivation of pyridoxal 5′-phosphate-dependent enzymes by 5-nitro-L-norvaline, an analogue of L-glutamate
    • TA Alston HJ Bright 1981 Inactivation of pyridoxal 5′-phosphate- dependent enzymes by 5-nitro-L-norvaline, an analogue of L-glutamate FEBS Lett 126 269 271
    • (1981) FEBS Lett , vol.126 , pp. 269-271
    • Alston, T.A.1    Bright, H.J.2
  • 3
    • 5044238127 scopus 로고    scopus 로고
    • A one-pot three-component synthesis of β-nitro-α-amino acids and their N-alkyl derivatives
    • PA Coghlan CJ Easton 1999a A one-pot three-component synthesis of β-nitro-α-amino acids and their N-alkyl derivatives J Chem Soc Perkin Trans 1 1999 2659 2660
    • (1999) J Chem Soc Perkin Trans 1 , vol.1999 , pp. 2659-2660
    • Coghlan, P.A.1    Easton, C.J.2
  • 4
    • 0033581016 scopus 로고    scopus 로고
    • β-Nitro-α-amino acids as latent α,β-dehydro- α-amino acid residues in peptides
    • PA Coghlan CJ Easton 1999b β-Nitro-α-amino acids as latent α,β-dehydro-α-amino acid residues in peptides Tetrahedron Lett 40 4745 4748
    • (1999) Tetrahedron Lett , vol.40 , pp. 4745-4748
    • Coghlan, P.A.1    Easton, C.J.2
  • 5
    • 5044228866 scopus 로고    scopus 로고
    • β-Nitro-α-amino acids as latent α,β-dehydro- α-amino acid residues in solid phase peptide synthesis
    • x
    • PA Coghlan CJ Easton 2004 β-Nitro-α-amino acids as latent α,β-dehydro-α-amino acid residues in solid phase peptide synthesis ARKIVOC 2004 x 101 108
    • (2004) ARKIVOC , vol.2004 , pp. 101-108
    • Coghlan, P.A.1    Easton, C.J.2
  • 6
    • 0029012572 scopus 로고
    • Synthesis of side-chain functionalized amino acid derivatives through reaction of alkyl nitronates with α-bromoglycine derivatives
    • CJ Easton PD Roselt ERT Tiekink 1995 Synthesis of side-chain functionalized amino acid derivatives through reaction of alkyl nitronates with α-bromoglycine derivatives Tetrahedron 51 7809 7822
    • (1995) Tetrahedron , vol.51 , pp. 7809-7822
    • Easton, C.J.1    Roselt, P.D.2    Tiekink, E.R.T.3
  • 7
    • 0001568267 scopus 로고
    • Chelation as a drving force in organic reactions. IV. Synthesis of α-nitro acids by control of the carboxylation-decarboxylation equilibrium
    • HL Finkbeiner M Stiles 1963 Chelation as a drving force in organic reactions. IV. Synthesis of α-nitro acids by control of the carboxylation-decarboxylation equilibrium J Am Chem Soc 85 616 622
    • (1963) J Am Chem Soc , vol.85 , pp. 616-622
    • Finkbeiner, H.L.1    Stiles, M.2
  • 8
    • 0022355317 scopus 로고
    • Substrate specificity of aspartate transcarbamylase
    • J Foote AM Lauritzen WN Lipscomb 1985 Substrate specificity of aspartate transcarbamylase J Biol Chem 260 9624 9629
    • (1985) J Biol Chem , vol.260 , pp. 9624-9629
    • Foote, J.1    Lauritzen, A.M.2    Lipscomb, W.N.3
  • 9
    • 0031055591 scopus 로고    scopus 로고
    • A new and practical synthesis of α-amino acids from alkenyl boronic acids
    • NA Petasis IA Zavialov 1997 A new and practical synthesis of α-amino acids from alkenyl boronic acids J Am Chem Soc 119 445 446
    • (1997) J Am Chem Soc , vol.119 , pp. 445-446
    • Petasis, N.A.1    Zavialov, I.A.2
  • 10
    • 0019332560 scopus 로고
    • 3-Carbanonic substrate analogues bind very tightly to fumarase and aspartase
    • DJT Porter HJ Bright 1980 3-Carbanonic substrate analogues bind very tightly to fumarase and aspartase J Biol Chem 255 4772 4780
    • (1980) J Biol Chem , vol.255 , pp. 4772-4780
    • Porter, D.J.T.1    Bright, H.J.2
  • 11
    • 0020804608 scopus 로고
    • Nitro analogs of substrates for adenylosuccinate synthetase and adenylosuccinate lyase
    • DJT Porter NG Rudie HJ Bright 1983 Nitro analogs of substrates for adenylosuccinate synthetase and adenylosuccinate lyase Arch Biochem Biophys 225 157 163
    • (1983) Arch Biochem Biophys , vol.225 , pp. 157-163
    • Porter, D.J.T.1    Rudie, N.G.2    Bright, H.J.3
  • 12
    • 0021473210 scopus 로고
    • Nitro analogs of substrates for argininosuccinate synthetase and argininosuccinate lyase
    • FM Raushel 1984 Nitro analogs of substrates for argininosuccinate synthetase and argininosuccinate lyase Arch Biochem Biophys 232 520 525
    • (1984) Arch Biochem Biophys , vol.232 , pp. 520-525
    • Raushel, F.M.1
  • 13
    • 0009106009 scopus 로고
    • Orientation in reactions of nitryl chloride and acrylic systems
    • H Shechter F Conrad AL Daulton RB Kaplan 1952 Orientation in reactions of nitryl chloride and acrylic systems J Am Chem Soc 74 3052 3056
    • (1952) J Am Chem Soc , vol.74 , pp. 3052-3056
    • Shechter, H.1    Conrad, F.2    Daulton, A.L.3    Kaplan, R.B.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.