Jump to main content
Jump to site search

Issue 26, 2014
Previous Article Next Article

Stereospecific [3+2] cycloaddition of 1,2-cyclopropanated sugars and ketones catalyzed by SnCl4: an efficient synthesis of multi-substituted perhydrofuro[2,3-b]furans and perhydrofuro[2,3-b]pyrans

Author affiliations

Abstract

Stereospecific [3+2] cycloaddition of 1,2-cyclopropanated sugars and ketones catalyzed by SnCl4 is described. The method offers multi-substituted perhydrofuro[2,3-b]furans (bis-THFs) and perhydrofuro[2,3-b]pyrans containing a quaternary carbon chiral center in good to excellent yields.

Graphical abstract: Stereospecific [3+2] cycloaddition of 1,2-cyclopropanated sugars and ketones catalyzed by SnCl4: an efficient synthesis of multi-substituted perhydrofuro[2,3-b]furans and perhydrofuro[2,3-b]pyrans

Back to tab navigation

Supplementary files

Publication details

The article was received on 24 Nov 2013, accepted on 06 Feb 2014 and first published on 06 Feb 2014


Article type: Communication
DOI: 10.1039/C3CC48963A
Author version available: Download Author version (PDF)
Citation: Chem. Commun., 2014,50, 3505-3508
  •   Request permissions

    Stereospecific [3+2] cycloaddition of 1,2-cyclopropanated sugars and ketones catalyzed by SnCl4: an efficient synthesis of multi-substituted perhydrofuro[2,3-b]furans and perhydrofuro[2,3-b]pyrans

    X. Ma, J. Zhang, Q. Tang, J. Ke, W. Zou and H. Shao, Chem. Commun., 2014, 50, 3505
    DOI: 10.1039/C3CC48963A

Search articles by author

Spotlight

Advertisements