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Search for "tetracyclic-fused" in Full Text gives 3 result(s) in Beilstein Journal of Organic Chemistry.

Recent synthesis of thietanes

  • Jiaxi Xu

Beilstein J. Org. Chem. 2020, 16, 1357–1410, doi:10.3762/bjoc.16.116

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  • -2,5-dithiones 347 gave tricyclic and tetracyclic fused thietane derivatives 348, 350, and 351 under photo irradiation [95] (Scheme 68). Nishio and co-workers investigated the photochemical [2 + 2] cycloaddition of vinyl 2-thioxo-3H-benzoxazole-3-carboxylate (353), affording the corresponding
  • tetracyclic fused benzoxazolethietane derivative 354 in 20% yield [83] (Scheme 69). In 1991, Sakomto and co-workers started on the synthesis of highly rigid thietane-fused β-lactams. They prepared various derivatives 356 in high yields via the photochemical cycloaddition reactions of N-(α,β-disubstituted
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Review
Published 22 Jun 2020

One-pot synthesis of tetracyclic fused imidazo[1,2-a]pyridines via a three-component reaction

  • Bo Yang,
  • Chuanye Tao,
  • Taofeng Shao,
  • Jianxian Gong and
  • Chao Che

Beilstein J. Org. Chem. 2016, 12, 1487–1492, doi:10.3762/bjoc.12.145

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  • -component reaction has been developed to assemble biologically and pharmaceutically important tetracyclic fused imidazo[1,2-a]pyridines in a one-pot fashion utilizing readily available 2-aminopyridines, isatins and isocyanides. The three-component coupling proceeds through the Groebke–Blackburn–Bienaymé
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Letter
Published 18 Jul 2016

An efficient access to the synthesis of novel 12-phenylbenzo[6,7]oxepino[3,4-b]quinolin-13(6H)-one derivatives

  • Wentao Gao,
  • Guihai Lin,
  • Yang Li,
  • Xiyue Tao,
  • Rui Liu and
  • Lianjie Sun

Beilstein J. Org. Chem. 2012, 8, 1849–1857, doi:10.3762/bjoc.8.213

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  • Wentao Gao Guihai Lin Yang Li Xiyue Tao Rui Liu Lianjie Sun Institute of Superfine Chemicals, Bohai University, Jinzhou 121000, China 10.3762/bjoc.8.213 Abstract An efficient access to the tetracyclic-fused quinoline systems, 12-phenylbenzo[6,7]oxepino[3,4-b]quinolin-13(6H)-one derivatives 4a–l
  • three-step route, offers easy access to tetracyclic-fused quinoline systems in short reaction times, and the products are obtained in moderate to good yields. Keywords: Eaton’s reagent; Friedel–Crafts acylation; Friedländer reaction; one-pot; PPA; quinoline; tetracyclic-fused; Introduction Polycyclic
  • thick and tight cell wall [46]. Altogether, the strategy using Eaton’s reagent instead of PPA showed a satisfactory conversion and gave us easy access to mono- and di-tert-butyl-substituted tetracyclic-fused quinoline systems. In addition, it is noteworthy that we also attempted additional experiments
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Published 30 Oct 2012
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