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Search for "xanthate transfer" in Full Text gives 3 result(s) in Beilstein Journal of Organic Chemistry.

Degenerative xanthate transfer to olefins under visible-light photocatalysis

  • Atsushi Kaga,
  • Xiangyang Wu,
  • Joel Yi Jie Lim,
  • Hirohito Hayashi,
  • Yunpeng Lu,
  • Edwin K. L. Yeow and
  • Shunsuke Chiba

Beilstein J. Org. Chem. 2018, 14, 3047–3058, doi:10.3762/bjoc.14.283

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  • ) using fac-Ir(ppy)3 (6) in DMSO under blue LED irradiation (λmax = 469 nm, Table 1, entry 1). As expected, the desired xanthate transfer was observed, while the process efficiency was not very high, forming 3aa in only 58% yield with incomplete conversion even after stirring for 20 h. Interestingly, we
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Full Research Paper
Published 13 Dec 2018

Some aspects of radical chemistry in the assembly of complex molecular architectures

  • Béatrice Quiclet-Sire and
  • Samir Z. Zard

Beilstein J. Org. Chem. 2013, 9, 557–576, doi:10.3762/bjoc.9.61

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  • processes. Keywords: amidyls; iminyls; radical allylation; radical vinylation; xanthate transfer; Introduction Natural products exhibit an astonishing diversity of molecular architectures and structural complexity. This has spurred the development of numerous synthetic strategies for the rapid assembly of
  • allowing intermolecular radical additions on unactivated alkenes, the xanthate transfer process opens infinite possibilities for bringing together various functional groups, which can then be made to react together. The functional groups can be present on the xanthate and/or the alkene partners. Over 2000
  • -diol on one of the alkenes would in principle result in the formation of a cyclic ketal. Spiro and cyclic ketals are ubiquitous in pheromones and in marine natural products [51]. The comparatively long effective lifetime of radicals generated under the conditions of the xanthate transfer may be
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Review
Published 18 Mar 2013

Ugi post-condensation copper-triggered oxidative cascade towards pyrazoles

  • Aurélie Dos Santos,
  • Laurent El Kaim,
  • Laurence Grimaud and
  • Caroline Ronsseray

Beilstein J. Org. Chem. 2011, 7, 1310–1314, doi:10.3762/bjoc.7.153

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  • , cyclocondensations and organometalic couplings, there was no existing description of radical processes on such adducts. Thus, we decided to undertake various studies using xanthate transfer [8][9][10], Mn(III) or copper(II) triggered oxidative couplings [11][12]. We recently reported a new synthesis of fused
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Letter
Published 21 Sep 2011
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