Carbenoid transfer reactions catalyzed by a ruthenium porphyrin macrocycle

TETRAHEDRON

卷:73

Article

van den Boomen, Onno I.¹  Coumans, Ruud G. E.¹  Akeroyd, Niels¹  Peters, Theo P. J.¹  Schiebos, Paul P. J.¹  Smits, Jan¹  de Gelder, Rene¹  Elemans, Johannes A. A. W.¹  Nolte, Roeland J. M.¹  Rowan, Alan E.^1,2 

[1] Radboud Univ Nijmegen, Inst Mol & Mat, Heyendaalseweg 135, NL-6525 AJ Nijmegen, Netherlands

[2] Univ Queensland, AIBN, Brisbane, Qld 4072, Australia

关键词: Rotaxanes;    Host-guest chemistry;    Ruthenium;    Porphyrins;    Carbenes;    C-H insertion;   

DOI  :  10.1016/j.tet.2017.05.035

来源: Elsevier

【 摘 要 】

A ruthenium porphyrin functionalized with a cavity based on diphenylglycoluril is applied as a catalyst in carbenoid transfer reactions using alpha-diazoesters as substrates. The latter compounds contain a blocking group connected via an alpha,omega-dioxyalkyl spacer of 3 or 6 carbon atoms. The reaction of an excess of the alpha-diazoester with the short spacer with the ruthenium porphyrin macrocycle leads to two products, a [2] rotaxane and a maleate ester, which are the result of dimerization reactions at the inside and the outside of the cavity, respectively. A similar reaction using the alpha-diazoester with the long spacer also yields high molecular weight species. Mass spectrometric and NMR studies suggest that C-H and/or C=C insertion reactions take place on the thread of the initially formed rotaxane. It is proposed that these reactions are favoured by effective molarity effects because of the close proximity of reactive species in the interlocked geometry. (C) 2017 Elsevier Ltd. All rights reserved.

【 授权许可】

Free