Pro-fluorescent ethynylthiophene-based o -nitrobenzyl photolabile protecting group for hydroxamic acid synthesis
Year: 2025
Type: article
Abstract: -NB PPGs in facilitating precise photoreactions under mild acidic conditions. Their pro-fluorescence response and minimal degradation under ambient conditions indicate their potential for application in releasing synthetically difficult-to-synthesize functional groups.
Source: Organic & Biomolecular Chemistry
DOI: 10.1039/d5ob00859j
Institutions: Kennesaw State University, Georgia State University
Language: English
Subfield: Materials Chemistry
Field: Materials Science
Domain: Physical Sciences
Open Access status: green
Awards: Track 4: Advanced CI Coordination Ecosystem: Monitoring and Measurement Services, G2184774346, CAREER: Shedding light on the Photochemistry of the LOV Class of Flavin Photoreceptors, Track 1: ACCESS Resource Allocations Marketplace and Platform Services (RAMPS), ACO: An Open CI Ecosystem to Advance Scientific Discovery (OpenCI), Track 3: COre National Ecosystem for CyberinfrasTructure (CONECT), Track 2: Customized Multi-tier Assistance, Training, and Computational Help (MATCH) for End User ACCESS to CI, LEAPS-MPS:Molecular Design, Synthesis, Properties, and Application of 2,5-bis(2-(4-nitrophenyl)ethynyl)thiophene Photolabile Protecting Groups for the Synthesis of Hydroxamic Acids, G9000003595
OpenAlex ID: W4413003067