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- Nickel-catalyzed reductive 1,3-diene formation from the cross-coupling of vinyl bromides. Yunfei Sha, Jiandong Liu, Liang Wang, Demin Liang, Da Wu, Hegui Gong
, Org. Biomol. Chem.
, 2021
, 19
, 4887
- 1-Bromoethene-1-sulfonyl fluoride (1-Br-ESF), a new SuFEx clickable reagent, and its application for regioselective construction of 5-sulfonylfluoro isoxazoles. Jing Leng, Hua-Li Qin
, Chem. Commun.
, 2018
, 54
, 4477
- Direct comparison of 3-centre and 4-centre HBr elimination pathways in methyl-substituted vinyl bromides. Shubhrangshu Pandit, Balázs Hornung, Andrew J. Orr-Ewing
, Phys. Chem. Chem. Phys.
, 2016
, 18
, 28353
- The reaction products of the 193 nm photolysis of vinyl bromide and vinyl chloride studied by time-resolved Fourier transform infrared emission spectroscopy. Antonio Carvalho, Gus Hancock, Mark Saunders
, Phys. Chem. Chem. Phys.
, 2006
, 8
, 4337
- Appendix. A table of dipole moments
, Trans. Faraday Soc.
, 1934
, 30
, B00i
- Ni-catalyzed reductive coupling of α-halocarbonyl derivatives with vinyl bromides. Canbin Qiu, Ken Yao, Xinghua Zhang, Hegui Gong
, Org. Biomol. Chem.
, 2016
, 14
, 11332
- Radical vinylation of dioxolanes and N-acylpyrrolidines using vinyl bromides. Takashi Kippo, Yuki Kimura, Ayami Maeda, Hiroshi Matsubara, Takahide Fukuyama, Ilhyong Ryu
, Org. Chem. Front.
, 2014
, 1
, 755
- 1-Bromoethene-1-sulfonyl fluoride (BESF) is another good connective hub for SuFEx click chemistry. Christopher J. Smedley, Marie-Claire Giel, Andrew Molino, Andrew S. Barrow, David J. D. Wilson, John E. Moses
, Chem. Commun.
, 2018
, 54
, 6020
- Microwave spectrum of monohalogenated allenes: bromoallene. Teruhiko Ogata, Yuzuru Niide
, J. Chem. Soc., Faraday Trans.
, 1992
, 88
, 3517
- 250. The Szilard–Chalmers reaction in ethylene dibromide. Miriam Milman, P. F. D. Shaw, I. B. Simpson
, J. Chem. Soc.
, 1957
, 1310