Synthesis of 4,8-anhydro-2,3-dideoxy-D-galacto- and D-gluco-non-3-enose dimethyl acetal and their use as new probes for determining by 1H-n.m.r. spectroscopy the steric course of protonation by glycoside hydrolases

  • Fritz H
  • Lehmann J
  • Schmidt-Schuchardt M
  • et al.
N/ACitations
Citations of this article
1Readers
Mendeley users who have this article in their library.

Cite

CITATION STYLE

APA

Fritz, H., Lehmann, J., Schmidt-Schuchardt, M., & Weiser, W. (1991). Synthesis of 4,8-anhydro-2,3-dideoxy-D-galacto- and D-gluco-non-3-enose dimethyl acetal and their use as new probes for determining by 1H-n.m.r. spectroscopy the steric course of protonation by glycoside hydrolases. Carbohydr. Res., 218, 129–141.

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