Preparation of fluoxetine by multiple flow processing steps

被引:27
作者
Ahmed-Omer, Batoul [1 ]
Sanderson, Adam J. [1 ]
机构
[1] Eli Lilly & Co Ltd, Lilly Res Ctr, Windlesham GU20 6PH, Surrey, England
关键词
MULTISTEP SYNTHESIS; BOND FORMATION; MICROFLUIDICS; REDUCTION; AZODICARBOXYLATE; MICROREACTOR; CHEMISTRY; DISCOVERY; REACTORS; LIPASES;
D O I
10.1039/c0ob00906g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Microflow technology is established as a modern and fashionable tool in synthetic organic chemistry, bringing great improvement and potential, on account of a series of advantages over flask methods. The study presented here focuses on the application of flow chemistry process in performing an efficient multiple step syntheses of (+/-)-fluoxetine as an alternative to conventional synthetic methods, and one of the few examples of total synthesis accomplished by flow technique.
引用
收藏
页码:3854 / 3862
页数:9
相关论文
共 46 条
  • [1] Enhancement of reaction rates by segmented fluid flow in capillary scale reactors
    Ahmed, Batoul
    Barrow, David
    Wirth, Thomas
    [J]. ADVANCED SYNTHESIS & CATALYSIS, 2006, 348 (09) : 1043 - 1048
  • [2] Advanced organic synthesis using microreactor technology
    Ahmed-Omer, Batoul
    Brandt, Johan C.
    Wirth, Thomas
    [J]. ORGANIC & BIOMOLECULAR CHEMISTRY, 2007, 5 (05) : 733 - 740
  • [3] AHMEDOMER B, 2011, ARKIVOC IN PRESS
  • [4] Barluenga J., 1987, J CHEM RES SYNOPSES, V12, P400
  • [5] The use of diethylaminosulfur trifluoride (DAST) for fluorination in a continuous-flow microreactor
    Baumann, Marcus
    Baxendale, Ian R.
    Ley, Steven V.
    [J]. SYNLETT, 2008, (14) : 2111 - 2114
  • [6] Azide monoliths as convenient flow reactors for efficient Curtius rearrangement reactions
    Baumann, Marcus
    Baxendale, Ian R.
    Ley, Steven V.
    Nikbin, Nikzad
    Smith, Christopher D.
    [J]. ORGANIC & BIOMOLECULAR CHEMISTRY, 2008, 6 (09) : 1587 - 1593
  • [7] Baxendale IR, 2006, CHIM OGGI, V24, P41
  • [8] A flow process for the multi-step synthesis of the alkaloid natural product oxomaritidine: a new paradigm for molecular assembly
    Baxendale, Ian R.
    Deeley, Jon
    Griffiths-Jones, Charlotte M.
    Ley, Steven V.
    Saaby, Steen
    Tranmer, Geoffrey K.
    [J]. CHEMICAL COMMUNICATIONS, 2006, (24) : 2566 - 2568
  • [9] Preparation of the neolignan natural product grossamide by a continuous-flow process
    Baxendale, IR
    Griffiths-Jones, CM
    Ley, SV
    Tranmer, GK
    [J]. SYNLETT, 2006, (03) : 427 - 430
  • [10] BAXENDALE IR, 2007, EMERGING TECHNOLOGIE