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Search for "solvent-free condition" in Full Text gives 4 result(s) in Beilstein Journal of Organic Chemistry.

Mechanochemistry of supramolecules

  • Anima Bose and
  • Prasenjit Mal

Beilstein J. Org. Chem. 2019, 15, 881–900, doi:10.3762/bjoc.15.86

Graphical Abstract
  • as the solvent-free condition may make traditional workup superfluous [31][32]. Also, mechanochemical methods have high impact in ecology and economy as they save time [33]. Mechanochemical syntheses benefit from high to quantitative conversions, minimized steps for purification and diminished
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Review
Published 12 Apr 2019

A green approach to the synthesis of novel phytosphingolipidyl β-cyclodextrin designed to interact with membranes

  • Yong Miao,
  • Florence Djedaïni-Pilard and
  • Véronique Bonnet

Beilstein J. Org. Chem. 2014, 10, 2654–2657, doi:10.3762/bjoc.10.278

Graphical Abstract
  • high reactant concentration and high temperatures used. The yield of the reaction performed in solvent-free condition is slightly lower than those obtained when conducted in DMF. This may be linked to the purification, since a large quantity of succinic anhydride was used in the reaction. Excess
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Letter
Published 12 Nov 2014

Silica sulfuric acid: a reusable solid catalyst for one pot synthesis of densely substituted pyrrole-fused isocoumarins under solvent-free conditions

  • Sudipta Pathak,
  • Kamalesh Debnath and
  • Animesh Pramanik

Beilstein J. Org. Chem. 2013, 9, 2344–2353, doi:10.3762/bjoc.9.269

Graphical Abstract
  • starting materials, and the excellent yields of products. Keywords: green chemistry; pyrrole-fused isocoumarin; reusable solid support; silica sulfuric acid; solvent-free condition; Introduction Isocoumarins are an important class of naturally occurring lactones [1][2][3], which has attracted the
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Full Research Paper
Published 04 Nov 2013

Synthesis of phenanthridines via palladium-catalyzed picolinamide-directed sequential C–H functionalization

  • Ryan Pearson,
  • Shuyu Zhang,
  • Gang He,
  • Nicola Edwards and
  • Gong Chen

Beilstein J. Org. Chem. 2013, 9, 891–899, doi:10.3762/bjoc.9.102

Graphical Abstract
  • . We commenced the study by investigating the arylation of 2-methoxybenzyl picolinamide 1 with 4-iodoanisole (2) under various conditions (Table 1) to form our desired arylated product 3. Our initial attempt under the original Pd(OAc)2-catalyzed AgOAc-promoted solvent-free condition afforded the
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Letter
Published 08 May 2013
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