Research output per year
Research output per year
Abstract
A robust N-nucleophilic 1,3-N,O-dipole equivalent reacts with unsymmetrical internal alkynes under gold catalysis. Conjugation from a remote nitrogen lone pair enables and controls this convergent and highly regioselective process. This journal is © 2013 The Royal Society of Chemistry.
| Original language | English |
|---|---|
| Pages (from-to) | 8617-8619 |
| Number of pages | 3 |
| Journal | Chemical Communications |
| Volume | 49 |
| Issue number | 77 |
| DOIs | |
| Publication status | Published - 7 Oct 2013 |
ASJC Scopus subject areas
- Organic Chemistry
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Dive into the research topics of 'Highly regioselective synthesis of 2,4,5-(hetero)aryl substituted oxazoles by intermolecular [3+2]-cycloaddition of unsymmetrical internal alkynes'. Together they form a unique fingerprint.-
Gold-catalyzed annulations with nucleophilic nitrenoids enabled by heteroatom-substituted alkynes
Davies, P., 27 Oct 2021, (E-pub ahead of print) In: The Chemical Record. 21, 12, p. 3964-3977Research output: Contribution to journal › Article › peer-review
Open AccessFile34 Downloads (Pure) -
Alkynyl Thioethers in Gold-Catalyzed Annulations to form Oxazoles
Davies, P., Jannapu Reddy, R. & Ball-Jones, M., 16 Oct 2017, In: Angewandte Chemie (International Edition) . 56, 43, p. 13310–13313Research output: Contribution to journal › Article › peer-review
Open AccessFile58 Citations (Scopus)161 Downloads (Pure) -
Efficient and flexible synthesis of highly functionalised 4-aminooxazoles by a gold-catalysed intermolecular formal [3+2]-dipolar cycloaddition
Davies, P., Gillie, A. & Jannapureddy, R., 21 Jan 2016, In: Advanced Synthesis & Catalysis. 358, 2, p. 226-239Research output: Contribution to journal › Article › peer-review
Open Access53 Citations (Scopus) -
Nucleophilic nitrenoids through π-acid catalysis: providing a common basis for rapid access into diverse nitrogen heterocycles
Davies, P. & Garzon Sanz, M., Aug 2015, In: Asian Journal of Organic Chemistry. 4, 8, p. 694-708 15 p.Research output: Contribution to journal › Review article › peer-review
Open AccessFile76 Citations (Scopus)281 Downloads (Pure)