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- Enantioselective copper catalysed C–H insertion reaction of 2-sulfonyl-2-diazoacetamides to form γ-lactams. Leslie Ann Clarke, Aoife Ring, Alan Ford, Abhijeet S. Sinha, Simon E. Lawrence, Anita R. Maguire
, Org. Biomol. Chem.
, 2014
, 12
, 7612
- Highly enantioselective synthesis of norcaradiene derivatives from naphthyl diazoacetamides using a Ru(ii)-Pheox complex. Nansalmaa Otog, Bilguun Gantogos, Ikuhide Fujisawa, Seiji Iwasa
, Chem. Commun.
, 2022
, 58
, 12325
- An expeditious synthesis of 4-alkoxycarbonyl-5-hydroxy-1,2,3-triazoles: the crystal and molecular structure of the 2-thienylammonium salt of 5-hydroxy-4-methoxycarbonyl-1-(2-thienyl)-1,2,3-triazole. Peter Murray-Rust, James McManus, Sean P. Lennon, Alexander E. A. Porter, Josef A. Rechka
, J. Chem. Soc., Perkin Trans. 1
, 1984
, 713
- Diazo compounds for the bioreversible esterification of proteins. Nicholas A. McGrath, Kristen A. Andersen, Amy K. F. Davis, Jo E. Lomax, Ronald T. Raines
, Chem. Sci.
, 2015
, 6
, 752
- Highly stereoselective intramolecular Buchner reaction of diazoacetamides catalyzed by a Ru(ii)–Pheox complex. Nga Phan Thi Thanh, Masaya Tone, Hayato Inoue, Ikuhide Fujisawa, Seiji Iwasa
, Chem. Commun.
, 2019
, 55
, 13398
- Alcohols, ethers and phenols. Trevor George, Ross Mabon, Gemma Sweeney, J. B. Sweeney, Ali Tavassoli
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 2529