Journal ArticleOPEN ACCESS

Convenient synthesis of 3',5'-cyclic diguanylic acid (cdiGMP).

Nucleic acids symposium series (2004) (2006) (50) 5-6
DOI: 10.1093/nass/nrl003
5Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

We herein report a convenient synthesis of 3',5'-cyclic diguanylic acid (cdiGMP) through the modified H-phosphonate chemistry. The 1-(4-chlorophenyl)-4-ethoxypiperidin-4-yl (Cpep) group was used as protecting group for the 2'-hydroxy functions of ribonucleosides. Homogeneous cdiGMP was obtained after removal of the protecting groups.

Cite

CITATION STYLE

APA

Yan, H., & Humes, E. (2006). Convenient synthesis of 3’,5’-cyclic diguanylic acid (cdiGMP). Nucleic Acids Symposium Series (2004), (50), 5–6. https://doi.org/10.1093/nass/nrl003

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