Search results

Search for "lipids" in Full Text gives 104 result(s) in Beilstein Journal of Organic Chemistry.

The development and evaluation of a continuous flow process for the lipase- mediated oxidation of alkenes

  • Charlotte Wiles,
  • Marcus J. Hammond and
  • Paul Watts

Beilstein J. Org. Chem. 2009, 5, No. 27, doi:10.3762/bjoc.5.27

Graphical Abstract
  • of the esterases [13]. Changes in enzymatic behaviour observed when lipases are employed in organic solvent systems have led to their use in the synthesis of lipids, carbohydrate esters, amines and amides, along with finding industrial application in the synthesis of pharmaceuticals, fine chemicals
PDF
Album
Full Research Paper
Published 02 Jun 2009

An expedient synthesis of 5-n-alkylresorcinols and novel 5-n-alkylresorcinol haptens

  • Kirsti Parikka and
  • Kristiina Wähälä

Beilstein J. Org. Chem. 2009, 5, No. 22, doi:10.3762/bjoc.5.22

Graphical Abstract
  • way for the immunochemical detection techniques of alkylresorcinols. Keywords: 5-n-alkylresorcinols; haptens; microwave assisted synthesis; Wittig reaction; Introduction 5-Alk(en)ylresorcinols and related compounds are phenolic lipids present in several families of plants (e.g. Gramineae
PDF
Album
Supp Info
Full Research Paper
Published 19 May 2009
Graphical Abstract
  • configuration (2S,3S) of the products is controlled by the chiral auxiliary. In recent years several studies on cell membrane lipid models suggested that ceramide could act indirectly as a messenger by modulation of membrane properties. The membrane lipids (mostly sphingomyelin) together with cholesterol are
  • networks, because its polar head groups can act both as acceptor and as a donor, ceramide, when added or generated in situ in the membrane, can segregate from the other lipids and cause coalescence of the small lipid raft domains to give highly ordered ceramide-enriched domains. Moreover, due to the small
PDF
Album
Supp Info
Full Research Paper
Published 25 Apr 2008

Transition- metal/Lewis acid free synthesis of acyl benzothiophenes via C-C bond forming reaction

  • Sarbani Pal,
  • Mohammad Ashrafuddin Khan,
  • P. Bindu and
  • P. K. Dubey

Beilstein J. Org. Chem. 2007, 3, No. 35, doi:10.1186/1860-5397-3-35

Graphical Abstract
  • lipids while displaying potent estrogen antagonist properties in the breast and uterus. A most common example of SERM is tamoxifen which has been the therapy of choice in the endocrine treatment of all stages of hormone-dependent breast cancer and in the primary and secondary chemoprevention of breast
PDF
Album
Supp Info
Preliminary Communication
Published 25 Oct 2007
Other Beilstein-Institut Open Science Activities