Issue 23, 2016

Lighting up sugars: fluorescent BODIPY–gluco-furanose and –septanose conjugates linked by direct B–O–C bonds

Abstract

We report the first O-BODIPY–glucose conjugates, in which the sugar is directly attached to the BODIPY boron through covalent B–O–C bonds. The reaction of Cl-BODIPY with glucose in acetonitrile produced the 1 : 1 α-glucofuranose BODIPY (1), 1 : 2 α-glucofuranose BODIPY (2) and 1 : 2 α-glucoseptanose BODIPY (3) esters. Compound 3 is a rare instance of the unnatural septanose form of glucose, and the first example of a septanose borate.

Graphical abstract: Lighting up sugars: fluorescent BODIPY–gluco-furanose and –septanose conjugates linked by direct B–O–C bonds

Supplementary files

Article information

Article type
Communication
Submitted
23 Mar 2016
Accepted
13 Apr 2016
First published
13 Apr 2016

Org. Biomol. Chem., 2016,14, 5205-5209

Lighting up sugars: fluorescent BODIPY–gluco-furanose and –septanose conjugates linked by direct B–O–C bonds

B. Liu, N. Novikova, M. C. Simpson, M. S. M. Timmer, B. L. Stocker, T. Söhnel, D. C. Ware and P. J. Brothers, Org. Biomol. Chem., 2016, 14, 5205 DOI: 10.1039/C6OB00726K

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