Chemical ligation from O-acyl isopeptides via 8-and 11-membered cyclic transition states

4Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.

Abstract

Unprotected O-acylated serine and O-acylated threonine isopeptides have been synthesized, and their conversion to native tripeptides and tetrapeptides by O-to N-terminus transfer investigated. Ligations involving 8-and 11-membered cyclic transition states are shown experimentally and computationally to be more favorable than intermolecular cross-ligations.© ARKAT-USA, Inc.

Cite

CITATION STYLE

APA

Panda, S. S., Elagawany, M., Marwani, H. M., Çalýakan, E., El Khatib, M., Oliferenko, A., … Katritzky, A. R. (2014). Chemical ligation from O-acyl isopeptides via 8-and 11-membered cyclic transition states. Arkivoc, 2014(4), 91–106. https://doi.org/10.3998/ark.5550190.p008.632

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