A photoresponsive glycosidase mimic

50Citations
Citations of this article
72Readers
Mendeley users who have this article in their library.

Abstract

Azobenzene-3,3’-dicarboxylic acid exists in photoisomerizable (E) and (Z)-forms. Deprotonation of the carboxylic acid groups from the (E)-form occurs simultaneously, whereas in the (Z)-form it occurs in a stepwise fashion. The mono anionic form of the (Z)-isomer acts as a glycosidase mimic that proceeds through a general acid-general base catalytic mechanism. This is the first example of a photoresponsive glycosidase mimic. © Partner Organisations 2014.

Cite

CITATION STYLE

APA

Samanta, M., Krishna, V. S. R., & Bandyopadhyay, S. (2014). A photoresponsive glycosidase mimic. Chemical Communications, 50(74), 10577–10579. https://doi.org/10.1039/c4cc03394a

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free