Synthesis of some new benzylic ethers from 1,8-cineole with antimicrobial activity

被引：11
|
作者：
Silvestre, AJD
Cavaleiro, JAS [1 ]
Feio, SS
Roseiro, JC
Delmond, B
Filliatre, C
机构：
[1] Univ Aveiro, Dept Chem, P-3810 Aveiro, Portugal
[2] Inst Nacl Engn & Tecnol Ind, IBQTA, Lab Microbiol Ind, P-1699 Lisbon, Portugal
[3] Univ Bordeaux 1, Inst Pin, F-33405 Talence, France
来源：
MONATSHEFTE FUR CHEMIE | 1999年 / 130卷 / 04期
关键词：
1,8-cineole; chemical transformation; 3-exo-benzyloxy-1,8-cineole; antimicrobial activity;
D O I：
10.1007/s007060050218
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
The synthesis and structural characterization of several benzylic derivatives of 3-exo-hydroxy-1,8-cineole is described. The new compounds show antimicrobial activity against Cladosporium cucumerinum, Staphylococcus aureus, Mycobacterium smegmatis, Pseudomonas aeruginosa, and Candida albicans.
引用
收藏
页码：589 / 595
页数：7
相关论文
共 50 条
  • [1] Synthesis of some new benzylic ethers from 1,8-cineole with antimicrobial activity [Synthese einiger neuer benzylether des 1,8-cineols mit antimikrobieller aktivität]
    Silvestre A.J.D.
    Cavaleiro J.A.S.
    Feio S.S.
    Roseiro J.C.
    Delmond B.
    Filliatre C.
    Monatshefte für Chemie / Chemical Monthly, 1999, 130 (4) : 589 - 595
  • [2] Antimicrobial activity of limonene enantiomers and 1,8-cineole alone and in combination
    Van Vuuren, S. F.
    Viljoen, A. M.
    FLAVOUR AND FRAGRANCE JOURNAL, 2007, 22 (06) : 540 - 544
  • [3] Biological Activity of 1,8-Cineole from Levant Wormwood
    Zh. K. Asanova
    E. M. Suleimenov
    G. A. Atazhanova
    A. D. Dembitskii
    R. N. Pak
    A. Dar
    S. M. Adekenov
    Pharmaceutical Chemistry Journal, 2003, 37 (1) : 28 - 30
  • [4] HYDROGENOLYSIS OF 1,8-CINEOLE
    HUGEL, HM
    JACKSON, WR
    KACHEL, CD
    RAE, ID
    AUSTRALIAN JOURNAL OF CHEMISTRY, 1977, 30 (06) : 1287 - 1292
  • [5] Synthesis and antibacterial activity of highly oxygenated 1,8-cineole derivatives
    Villecco, Margarita B.
    Catalan, Julieta V.
    Vega, Marta I.
    Garibotto, Francisco M.
    Enriz, Ricardo D.
    Catalan, Cesar A. N.
    NATURAL PRODUCT COMMUNICATIONS, 2008, 3 (03) : 303 - 312
  • [6] Synthesis of 1,8-Cineole Derivatives from 3-Carene
    Wang, Jing
    Zhang, Hongmei
    Xu, Shichao
    Jiang, Jianxin
    Chen, Yuxiang
    Zhao, Zhendong
    CHEMISTRYSELECT, 2021, 6 (33): : 8640 - 8644
  • [7] REARRANGEMENTS OF 1,8-CINEOLE DERIVATIVES
    BONDAVALLI, F
    CHIMICA & L INDUSTRIA, 1978, 60 (01): : 66 - 67
  • [8] 1,8-CINEOLE FROM ALPHA-TERPINEOL
    COXON, JM
    HARTSHOR.MP
    MITCHELL, JW
    RICHARDS, KE
    CHEMISTRY & INDUSTRY, 1968, (20) : 652 - &
  • [9] HYDROXYCINEOLE - 4 NEW METABOLITES OF 1,8-CINEOLE IN RABBITS
    MIYAZAWA, M
    KAMEOKA, H
    MORINAGA, K
    NEGORO, K
    MURA, N
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1989, 37 (01) : 222 - 226
  • [10] Application of additives in 1,8-cineole purification
    Liu, Keguo
    Gu, Lili
    Hu, Huiguang
    Yang, Rong
    Tao, Jun
    ADVANCES IN CHEMICAL, MATERIAL AND METALLURGICAL ENGINEERING, PTS 1-5, 2013, 634-638 : 382 - 385
12345