An Investigation of Wall Effects in Microwave-Assisted Ring-Closing Metathesis and Cyclotrimerization Reactions

被引:50
|
作者
Dallinger, Doris
Irfan, Muhammed
Suljanovic, Amra
Kappe, C. Oliver [1 ]
机构
[1] Karl Franzens Univ Graz, CDLMC, A-8010 Graz, Austria
来源
JOURNAL OF ORGANIC CHEMISTRY | 2010年 / 75卷 / 15期
关键词
CATALYZED OLEFIN METATHESIS; CROSS-METATHESIS; ALKYNE CYCLOTRIMERIZATION; ENANTIOSELECTIVE SYNTHESIS; 2+2+2 CYCLOADDITION; HIGHLY EFFICIENT; GENERAL-APPROACH; RCM; DERIVATIVES; CHEMISTRY;
D O I
10.1021/jo1011703
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Challenging Ru-catalyzed ring-closing metathesis transformations leading to eight-membered-ring systems and Ni- or Co-catalyzed [2+2+2] cyclotrimerizations were evaluated at elevated temperatures applying microwave dielectric heating or conventional thermal heating in order to investigate the role of wall effects. All reactions were conducted in a dedicated reactor setup that allowed accurate internal reaction temperature measurements using fiber-optic probes for both types of heating modes. For ring-closing metathesis best results were achieved using an open vessel gas sparging protocol in 1,2-dichloroethane at reflux temperature (83 degrees C), while cyclotrimerizations were performed under sealed vessel conditions in toluene between 80 and 160 degrees C. For all studied transformations the results achieved in a single-mode microwave reactor could be reproduced by conventional heating in an oil bath by carefully matching the temperature profiles as close as possible during the entire heating and cooling cycle. In contrast to previous literature reports, no evidence that direct in-core microwave heating can increase catalyst lifetime by minimization or elimination of wall effects was obtained. At the same time, no indication for the involvement of nonthermal microwave effects in these homogeneous transition metal-catalyzed transformations was seen.
引用
收藏
页码:5278 / 5288
页数:11
相关论文
共 50 条
  • [31] Ring-closing reactions
    不详
    ACTUALITE CHIMIQUE, 2003, (4-5): : 45 - 45
  • [32] Optimization of ring-closing metathesis: Inert gas sparging and microwave irradiation
    Nosse, B
    Schall, A
    Jeong, WB
    Reiser, O
    ADVANCED SYNTHESIS & CATALYSIS, 2005, 347 (14) : 1869 - 1874
  • [33] Ring-closing metathesis in methanol and water
    Kirkland, TA
    Lynn, DM
    Grubbs, RH
    JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (26): : 9904 - 9909
  • [34] Oligomers as intermediates in ring-closing metathesis
    Conrad, Jay C.
    Eelman, Melanie D.
    Duarte, Silva, Joao A.
    Monfette, Sebastien
    Parnas, Henrietta H.
    Snelgrove, Jennifer L.
    Fogg, Deryn E.
    Journal of the American Chemical Society, 2007, 129 (05): : 1024 - 1025
  • [35] Synthesis of Sultams by Ring-Closing Metathesis
    Mondal, Shovan
    Debnath, Sudarshan
    SYNTHESIS-STUTTGART, 2014, 46 (03): : 368 - 374
  • [36] Ring-closing metathesis in carbohydrate annulation
    Holt, DJ
    Barker, WD
    Jenkins, PR
    Davies, DL
    Garratt, S
    Fawcett, J
    Russell, DR
    Ghosh, S
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1998, 37 (23) : 3298 - 3300
  • [37] Quantitative ring-closing metathesis of polyolefins
    Coates, GW
    Grubbs, RH
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (01) : 229 - 230
  • [38] A New Approach to Inducing Silicon Tethered Ring-closing Metathesis Reactions
    YANG Hong-li * and VAULTIER MichelSynthèse et Electrosynthèse Organiques
    Chemical Research in Chinese Universities, 2002, (04) : 414 - 418
  • [39] Tandem ring-closing metathesis/isomerization reactions for the total synthesis of violacein
    Petersen, Mette T.
    Nielsen, Thomas E.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2013, 245
  • [40] Allylmalonate as an Activator Subunit for the Initiation of Relay Ring-Closing Metathesis Reactions
    Hoye, Thomas R.
    Jeon, Junha
    Tennakoon, Manomi A.
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (09) : 2141 - 2143