Urethane-protected alpha-amino acid N-carboxyanhydrides and peptide synthesis

被引:0
|
作者
Fuller, WD
Goodman, M
Naider, FR
Zhu, YF
机构
[1] UNIV CALIF SAN DIEGO,DEPT CHEM & BIOCHEM,LA JOLLA,CA 92093
[2] CUNY COLL STATEN ISL,DEPT CHEM,STATEN ISL,NY 10314
关键词
D O I
10.1002/(SICI)1097-0282(1996)40:2<183::AID-BIP1>3.0.CO;2-S
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The preparation, physical properties and analytical data are reported for seventy urethane-protected (Boc, Cbz, FMOC) amino acid N-carboxyanhydrides (UNCAs). Most of the UNCAs are crystalline and the X-ray diffraction patterns for several of these are described. UNCAs are stable to routine laboratory manipulations and can be stored for extended periods of time (1-2 years at below 0 degrees C). Most are completely stable to the conditions commonly employed for peptide synthesis. The correct choice of base is key for the successful introduction of urethane protecting groups into NCAs. N-Methylmorpholine is used for the introduction of FMOC, Cbz or Boc from the chloroformates, and pyridine is used for the introduction of the Boc group from Boc anhydride. UNCAs represent a unique class of preactivated, isolable and stable amino acid derivatives that generate no side products or co-products, other than CO2, during condensation reactions. The application of UNCAs in peptide synthesis in both solid phase and in solution is reviewed in detail. (C) 1996 John Wiley & Sons, Inc.
引用
收藏
页码:183 / 205
页数:23
相关论文
共 50 条
  • [41] Scaffold directed cooperative polymerization of amino acid N-carboxyanhydrides
    Baumgartner, Ryan
    Cheng, Jianjun
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2017, 254
  • [42] N-2-NITROPHENYLSULFENYL AMINO-ACID N-CARBOXYANHYDRIDES
    HALSTROM, J
    BRUNFELD.K
    KOVACS, K
    HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1974, 355 (01): : 82 - 84
  • [43] Base-induced dimerization of urethane-protected amino acid. N-carboxanhydrides
    Leban, JJ
    Colson, KL
    JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (01): : 228 - 231
  • [44] Polypeptides and 100 years of chemistry of α-amino acid N-carboxyanhydrides
    Kricheldorf, Hans R.
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (35) : 5752 - 5784
  • [45] A micro-flow rapid dual activation approach for urethane-protected α-amino acid N-carboxyanhydride synthesis
    Okabe, Ren
    Sugisawa, Naoto
    Fuse, Shinichiro
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2022, 20 (16) : 3303 - 3310
  • [46] APPLICATION OF N-(TERT-BUTYLOXYCARBONYL)AMINO ACID N-CARBOXYANHYDRIDES IN SOLID-PHASE PEPTIDE-SYNTHESIS
    XUE, CB
    NAIDER, F
    JOURNAL OF ORGANIC CHEMISTRY, 1993, 58 (02): : 350 - 355
  • [47] Cyclic polypeptides by thermal polymerization of α-amino acid N-carboxyanhydrides
    Kricheldorf, Hans R.
    Lossow, Colin V.
    Lomadze, Nino
    Schwarz, Gert
    JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2008, 46 (12) : 4012 - 4020
  • [48] Nickel mediated grafting from polymerization of alpha-amino acid-N-carboxyanhydrides.
    Menzel, H
    Witte, P
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2003, 225 : U600 - U600
  • [49] OZONOLYSIS OF ETHYLIDENE AZETIDINONES - OZONIDE FRAGMENTATION TO ALPHA-AMINO ACID-N-CARBOXYANHYDRIDES
    BATESON, JH
    KAURA, AC
    SOUTHGATE, R
    TETRAHEDRON LETTERS, 1991, 32 (18) : 2065 - 2068
  • [50] Regioselective reaction of unprotected sugars with urethane N-carboxyanhydrides for the synthesis of new surfactants
    Bellhaouel, S
    Roumestant, ML
    Viallefont, P
    Martinez, J
    SYNTHETIC COMMUNICATIONS, 2002, 32 (02) : 181 - 187