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- N-Nosyl-O-bromoethyl hydroxylamine acts as a multifunctional formaldehyde, formaldimine, and 1,2-oxazetidine surrogate for C–C and C–O bond-forming reactions. Binyu Wu, Xiaolu Wen, Hongbing Chen, Lin Hu
, Org. Chem. Front.
, 2021
, 8
, 5124
- Nuclear magnetic resonance studies of heterocyclic fluorine compounds. Part 1.—Oxazetidines and oxazines. J. Lee, K. G. Orrell
, Trans. Faraday Soc.
, 1965
, 61
, 2342
- 1044. Polyhalogeno-allenes. Part II. Reaction of tetrafluoroallene with trifluoronitrosomethane. R. E. Banks, R. N. Haszeldine, D. R. Taylor
, J. Chem. Soc.
, 1965
, 5602
- Perfluoroalkyl derivatives of nitrogen. Part I. Perfluoro-2-methyl-1 : 2-oxazetidine and perfluoro(alkylenealkylamines). D. A. Barr, R. N. Haszeldine
, J. Chem. Soc.
, 1955
, 1881
- Polyfluoroalkyl derivatives of nitrogen. Part XXXIII. The kinetics of the reaction between trifluoronitrosomethane and tetrafluorethylene to form perfluoro-2-methyl-1,2-oxazetidine. J. D. Crabtree, R. N. Haszeldine, K. Ridings, R. F. Simmons, S. Smith
, J. Chem. Soc., Perkin Trans. 2
, 1972
, 119
- Proton-assisted ring opening of a 2,3-dialkyl-4-alkylimino-1,2-oxazetidine. Dietrich Moderhack, Michael Lorke
, J. Chem. Soc., Chem. Commun.
, 1977
, 831
- 663. Perfluoroalkyl derivatives of nitrogen. Part III. Heptafluoronitrosopropane, perfluoro-2-n-propyl-1 : 2-oxazetidine, perfluoro-(methylene-n-propylamine), and related compounds. D. A. Barr, R. N. Haszeldine
, J. Chem. Soc.
, 1956
, 3416
- Merging strain-release and copper catalysis: the selective ring-opening cross-coupling of 1,2-oxazetidines with boronic acids. Ji-Hang Xu, Zi-Kui Liu, Yan-Liu Tang, Yang Gao, Xiao-Qiang Hu
, Chem. Commun.
, 2022
, 58
, 4180
- 584. Perfluoroalkyl derivatives of nitrogen. Part X. The reaction of nitric oxide with tetrafluoroethylene, and formation of a nitrosopolymer. J. M. Birchall, A. J. Bloom, R. N. Haszeldine, C. J. Willis
, J. Chem. Soc.
, 1962
, 3021
- Merging alkenyl C–H activation with the ring-opening of 1,2-oxazetidines: ruthenium-catalyzed aminomethylation of enamides. Song Li, Qi-Chao Shan, Lu-Min Hu, Xue-Qing Ma, Xu-Hong Hu
, Chem. Commun.
, 2020
, 56
, 7969