Metallkomplexe mit biologisch wichtigen Liganden. CLVII [1] Halbsandwich-Komplexe mit Isocyanoacetylaminosäureestern und Isocyanoacetyldi- und tripeptidestern („Isocyano-Peptide”)

作者: Markus A. Lang , Wolfgang Beck

DOI: 10.1002/ZAAC.200500257

关键词:

摘要: Metal Complexes of Biologically Important Ligands, CLVII [1] Halfsandwich Isocyanoacetylamino acid esters and Isocyanoacetyldi- tripeptide („Isocyanopeptides”) N-Isocyanoacetyl-amino CNCH2C(O) NHCH(R)CO2CH3 (R = CH3, CH(CH3)2, CH2CH(CH3)2, CH2C6H5) N-isocyanoacetyl-di- CNCH2C(O)NHCH(R1)C(O)NHCH(R2)CO2C2H5 CNCH2C(O)NHCH(R1)C(O)NHCH (R2)C(O)NHCH(R3)CO2CH3 (R1 R2 R3 CH2C6H5, H, are available by condensation potassium isocyanoacetate with amino or peptide esters. These isocyanides form chloro-bridged complexes [(arene)M(Cl)(μ-Cl)]2 (arene Cp*, p-cymene, M Ir, Rh, Ru) in the presence Ag[BF4] Ag[CF3SO3] cationic halfsandwich [(arene)M(isocyanide)3]+X− (X BF4, CF3SO3).

参考文章(19)
Jeroen J. L. M. Cornelissen, W. Sander Graswinckel, Alan E. Rowan, Nico A. J. M. Sommerdijk, Roeland J. M. Nolte, Conformational Analysis of Dipeptide-Derived Polyisocyanides Journal of Polymer Science Part A. ,vol. 41, pp. 1725- 1736 ,(2003) , 10.1002/POLA.10713
Inga Hoppe, Ulrich Schöllkiof, Cycloaddition von “Isocyanketen” an Benzophenonanil und Thioimidsäureester zu β-Lactamen Chemische Berichte. ,vol. 109, pp. 482- 487 ,(1976) , 10.1002/CBER.19761090210
N.I. Gorshkov, R. Schibli, A.P. Schubiger, A.A. Lumpov, A.E. Miroslavov, D.N. Suglobov, “2 + 1” Dithiocarbamate–isocyanide chelating systems for linking M(CO)3+ (M = 99mTc, Re) fragment to biomolecules Journal of Organometallic Chemistry. ,vol. 689, pp. 4757- 4763 ,(2004) , 10.1016/J.JORGANCHEM.2004.09.019
Basanagoud S Patil, Ganga-Ramu Vasanthakumar, VV Suresh Babu, None, Synthesis of β-Amino Acids: 2-(1H-Benzotriazol-1-yl)-1,1,3,3-tetramethyluronium Tetrafluoroborate (TBTU) for Activation of Fmoc-/Boc-/Z-α-Amino Acids Synthetic Communications. ,vol. 33, pp. 3089- 3096 ,(2003) , 10.1081/SCC-120023410
Reinhard Urban, Dieter Marquarding, Peter Seidel, Ivar Ugi, Annette Weinelt, Notiz zur Synthese optisch aktiver α‐Isocyancarbonsäure‐Derivate für Peptidsynthesen mittels Vier‐Komponenten‐Kondensation (4 CC) Chemische Berichte. ,vol. 110, pp. 2012- 2015 ,(1977) , 10.1002/CBER.19771100545
Ken-ichi NUNAMI, Mamoru SUZIKI, Kazuo MATSUMOTO, Naoto YONEDA, Kazuo TAKIGUCHI, Syntheses and Biological Activities of Isonitrile Dipeptides Agricultural and biological chemistry. ,vol. 48, pp. 1073- 1075 ,(1984) , 10.1271/BBB1961.48.1073
Akihiro Nomoto, Toshiyuki Moriuchi, Shuhei Yamazaki, Akiya Ogawa, Toshikazu Hirao, A highly ordered ferrocene system regulated by podand peptide chains Chemical Communications. pp. 1963- 1964 ,(1998) , 10.1039/A805780J
Kazuo MATSUMOTO, Mamoru SUZUKI, Naoto YONEDA, Muneji MIYOSHI, Alkylation of α-Isocyanoacetamides; Synthesis of 1,4,4-Trisubstituted 5-Oxo-4,5-dihydroimidazoles1 Synthesis. ,vol. 1977, pp. 249- 250 ,(1977) , 10.1055/S-1977-24337
Jeroen JLM Cornelissen, Matthias Fischer, Nico AJM Sommerdijk, Roeland JM Nolte, Helical Superstructures from Charged Poly(styrene)-Poly(isocyanodipeptide) Block Copolymers Science. ,vol. 280, pp. 1427- 1430 ,(1998) , 10.1126/SCIENCE.280.5368.1427