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Search for "reduction reaction" in Full Text gives 28 result(s) in Beilstein Journal of Organic Chemistry.

Miniemulsion polymerization as a versatile tool for the synthesis of functionalized polymers

  • Daniel Crespy and
  • Katharina Landfester

Beilstein J. Org. Chem. 2010, 6, 1132–1148, doi:10.3762/bjoc.6.130

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  • droplets followed by polymerization of the dispersed phase [22]. The reduction reaction was performed at high temperature and miniemulsions were kept stable. This novel system opens up the area of high temperature reactions in miniemulsion. Acrylic acid was also copolymerized with trivinylacrylic acid in
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Published 01 Dec 2010

Prediction of reduction potentials from calculated electron affinities for metal-salen compounds

  • Sarah B. Bateni,
  • Kellie R. England,
  • Anthony T. Galatti,
  • Handeep Kaur,
  • Victor A. Mendiola,
  • Alexander R. Mitchell,
  • Michael H. Vu,
  • Benjamin F. Gherman and
  • James A. Miranda

Beilstein J. Org. Chem. 2009, 5, No. 82, doi:10.3762/bjoc.5.82

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  • then the opposite of the enthalpy change for the 1-electron reduction reaction (Equation 2). The choice of density functional to employ here was made from among the pure density functionals BLYP [14][15], OLYP [15][16], and HCTH [17] and the hybrid density functionals B3LYP [14][15][18], O3LYP [15][16
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Preliminary Communication
Published 23 Dec 2009

Knorr- Rabe partial reduction of pyrroles: Application to the synthesis of indolizidine alkaloids

  • Brendon S. Gourlay,
  • John H. Ryan and
  • Jason A. Smith

Beilstein J. Org. Chem. 2008, 4, No. 3, doi:10.1186/1860-5397-4-3

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  • intermediate. Donohoe's approach to (±)-1-epiaustraline utilising a modified Birch reduction. Reaction conditions i) Zn, HCl (aq). Reaction conditions: i) ref. [10] ii) ref. [11] iii) Zn, conc. HCl(aq). Potential mechanism for α-ketopyrrole reduction.. Alternative reduction pathway. Catalytic hydrogenation
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Published 15 Jan 2008
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