Search results

Search for "organofluorine" in Full Text gives 79 result(s) in Beilstein Journal of Organic Chemistry.

Synthesis of deep- cavity fluorous calix[4]arenes as molecular recognition scaffolds

  • Maksim Osipov,
  • Qianli Chu,
  • Steven J. Geib,
  • Dennis P. Curran and
  • Stephen G. Weber

Beilstein J. Org. Chem. 2008, 4, No. 36, doi:10.3762/bjoc.4.36

Graphical Abstract
  • ; organofluorine; (perfluoroalkyl)alkyl aryl ethers; Introduction Calixarenes [1] are one of the most useful types of macrocyclic scaffolds. Since first reported by Zinke and Ziegler [2], calix[4]arenes have been used for a variety of molecular recognition, nanotechnology, and supramolecular applications. These
PDF
Album
Supp Info
Full Research Paper
Published 20 Oct 2008
Graphical Abstract
  • Chuanfa Ni Fang Wang Jinbo Hu Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, China 10.3762/bjoc.4.21 Abstract Background Although the nucleophilic difluoromethylation of aldehydes, ketones, and
  • −, the fluorine substitution being commonly on the carbanion center) to an electrophile, represents one of the major methods for the synthesis of organofluorine compounds [4][5][6][7][8][9][10][11][12][13][14][15][16][17][18]. In recent years, a few methods have been reported for the enantioselective
PDF
Album
Supp Info
Full Research Paper
Published 26 Jun 2008

Understanding the mechanism of Pd-catalyzed allylic substitution of the cyclic difluorinated carbonates

  • Jun Xu,
  • Xiao-Long Qiu and
  • Feng-Ling Qing

Beilstein J. Org. Chem. 2008, 4, No. 18, doi:10.3762/bjoc.4.18

Graphical Abstract
  • Jun Xu Xiao-Long Qiu Feng-Ling Qing Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, 2999 North Renmin Lu
PDF
Album
Supp Info
Full Research Paper
Published 27 May 2008

Stereoselective α-fluoroamide and α-fluoro- γ-lactone synthesis by an asymmetric zwitterionic aza-Claisen rearrangement

  • Kenny Tenza,
  • Julian S. Northen,
  • David O'Hagan and
  • Alexandra M. Z. Slawin

Beilstein J. Org. Chem. 2005, 1, No. 13, doi:10.1186/1860-5397-1-13

Graphical Abstract
  • purity.[11] Successes in this area has advanced methodology in organofluorine chemistry considerably over the last decade or so.[1][2] In this paper we explore an alternative approach for the preparation of α-fluorocarbonyls using an asymmetric zwitterionic aza-Claisen rearrangement on appropriate
PDF
Album
Full Research Paper
Published 17 Oct 2005
Other Beilstein-Institut Open Science Activities