Synthesis of Chiral 3,4-Disubstituted Pyrrolidines with Antibacterial Properties

被引:9
|
作者
Rodriguez, Lenka [1 ]
Fisera, Roman [1 ]
Gaalova, Barbora [2 ]
Koci, Kamila [2 ]
Bujdakova, Helena [2 ]
Meciarova, Maria [3 ]
Gorova, Renata [4 ]
Jurdakova, Helena [4 ]
Sebesta, Radovan [3 ]
机构
[1] SYNKOLA Ltd, Ilkovicova 6, Bratislava 84215, Slovakia
[2] Comenius Univ, Fac Nat Sci, Dept Microbiol, Ilkovicova 6, Bratislava 84215, Slovakia
[3] Comenius Univ, Fac Nat Sci, Dept Organ Chem, Ilkovicova 6, Bratislava 84215, Slovakia
[4] Comenius Univ, Fac Nat Sci, Inst Chem, Ilkovicova 6, Bratislava 84215, Slovakia
关键词
Asymmetric Organocatalysis; Michael addition; Reductive Cyclization; Pyrrolidine; Antibacterial Activity; ORGANOCATALYTIC MICHAEL ADDITIONS; SILYL ETHERS; ANTIBIOTIC-RESISTANCE; AZOMETHINE YLIDES; ALDEHYDES; DERIVATIVES; CATALYSTS; NITROALKENES; OXYACETALDEHYDES; NITROOLEFINS;
D O I
10.1002/ejoc.202000235
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Chiral aliphatic heterocycles are important structural feature of many pharmaceutical agents. Antibiotic resistance is a serious medical problem, therefore new antibacterial compounds are urgently needed. Herein, we describe synthesis of a series of 3,4-disubstituted pyrrolidine derivatives via organocatalytic Michael addition followed by reductive cyclization. These compounds inhibited growth of standard as well as methicillin-resistant strains of Escherichia coli and Staphylococcus aureus.
引用
收藏
页码:2565 / 2575
页数:11
相关论文
共 50 条
  • [31] CHIRAL SYNTHESIS OF 3,4-DISUBSTITUTED 2-AZETIDINONES FROM (R,R)-(+)-TARTARIC ACID
    GATEAUOLESKER, A
    CLEOPHAX, J
    GERO, SD
    TETRAHEDRON LETTERS, 1986, 27 (01) : 41 - 44
  • [32] A CONVENIENT METHOD FOR THE SYNTHESIS OF UNSYMMETRICAL 3,4-DISUBSTITUTED PYRROLES
    SHUM, PW
    KOZIKOWSKI, AP
    TETRAHEDRON LETTERS, 1990, 31 (47) : 6785 - 6788
  • [33] Synthesis of 3,4-disubstituted 4-aminobutanoic acids
    O. S. Vasil’eva
    E. S. Ostroglyadov
    A. A. Nikonorov
    O. V. Komarova
    V. M. Berestovitskaya
    Russian Journal of Organic Chemistry, 2016, 52 : 904 - 905
  • [34] Synthesis of 3,4-disubstituted pyrrole amino acids.
    Mapes, CM
    Nemeroff, NH
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1996, 211 : 309 - CHEN
  • [35] A novel and simple route for the synthesis of 3,4-disubstituted pyrroles
    Padmavathi, V
    Reddy, BJM
    Padmaja, A
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 2005, 42 (02) : 333 - 335
  • [36] Synthesis and characterization of 3-substituted and 3,4-disubstituted thiophenes
    Tong, LG
    Jian, XG
    Wang, JY
    Yu, Y
    CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2004, 24 (01) : 67 - 70
  • [37] Synthesis of 3,4-disubstituted 4-aminobutanoic acids
    Vasil'eva, O. S.
    Ostroglyadov, E. S.
    Nikonorov, A. A.
    Komarova, O. V.
    Berestovitskaya, V. M.
    RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2016, 52 (06) : 904 - 905
  • [38] Some 3,4-disubstituted pyridmes
    Webb, JL
    Corwin, AH
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1944, 66 : 1456 - 1459
  • [39] Pharmacophore-based discovery of 3,4-disubstituted pyrrolidines as a novel glass of monoamine transporter inhibitors
    Enyedy, IJ
    Zaman, WA
    Sakamuri, S
    Kozikowski, AP
    Johnson, KM
    Wang, SM
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2001, 11 (09) : 1113 - 1118
  • [40] 3,4-DISUBSTITUTED FURANS .3. LITHIATION OF 3,4-BIS(TRI-N-BUTYLSTANNYL)FURAN - REGIOSPECIFIC SYNTHESIS OF UNSYMMETRICAL 3,4-DISUBSTITUTED FURANS
    YANG, Y
    WONG, HNC
    JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1992, (23) : 1723 - 1725