Traceless Release of Alcohols Using Thiol-Sensitive Oxanorbornadiene Linkers
Author:
Affiliation:
1. School of Chemistry & Biochemistry, School of Biological Sciences, Georgia Institute of Technology, 901 Atlantic Drive, Atlanta, Georgia 30332, United States
Funder
Division of Chemistry
Georgia Institute of Technology
National Science Foundation
Children's Healthcare of Atlanta
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b01093
Reference21 articles.
1. Thiol-Selective Fluorogenic Probes for Labeling and Release
2. Albumin-Oxanorbornadiene Conjugates Formed ex Vivo for the Extended Circulation of Hydrophilic Cargo
3. Degradable Conjugates from Oxanorbornadiene Reagents
4. Theoretical Analysis of the Retro-Diels–Alder Reactivity of Oxanorbornadiene Thiol and Amine Adducts
5. A thermally-cleavable linker for solid-phase synthesis
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