ORCID Profile
0000-0002-4404-4895
Current Organisation
University of York
Does something not look right? The information on this page has been harvested from data sources that may not be up to date. We continue to work with information providers to improve coverage and quality. To report an issue, use the Feedback Form.
Publisher: Wiley
Date: 20-06-2023
Abstract: A synthetic strategy that exploits the formation of an electron donor‐acceptor (EDA) complex between a tertiary α‐ silylamine and 1‐iodoalkyne under UVA LED (light emitting diode) light ( λ max =365 nm) to prepare propargyl amines is described. The site‐ and chemoselective synthetic method was shown to tolerate a wide range of functional groups to give the α ‐alkynylation product in good to excellent yields. The usefulness of the C(sp)–C(sp 3 ) bond formation protocol was also exemplified by the late‐stage functionalisation of a variety of natural products and bioactive compounds.
Publisher: Wiley
Date: 10-07-2023
Abstract: A synthetic method to prepare 1,2‐diamines efficiently that relies on the 4CzPN‐catalysed α ‐aminoalkylation of azomethine imines by secondary and tertiary α ‐silylamines under blue light emitting diode (LED) light (456 nm) is described. Achieved under metal‐ and additive‐free reaction conditions at room temperature, the synthetic protocol was shown to afford product yields up to 99% and applicable to the late‐stage functionalisation of three drug molecules and the gramme‐scale preparation of one ex le.
Publisher: Royal Society of Chemistry (RSC)
Date: 2023
DOI: 10.1039/D3NJ03780K
Publisher: Springer Science and Business Media LLC
Date: 17-01-2017
Location: China
Location: United Kingdom of Great Britain and Northern Ireland
Location: United Kingdom of Great Britain and Northern Ireland
Location: United Kingdom of Great Britain and Northern Ireland
No related grants have been discovered for jiacheng li.