![Ni(II) complexes with thioether-functionalized silylamide ligands. Synthesis and crystal structures of [Ni{Me2Si(N-C6H4-2-S-t-Bu)2}], [Ni{Ph2Si(N-C6H4-2-SMe)2}] and [Ni{Ph2Si(N-C6H4-2-SPh)2}] Ni(II) complexes with thioether-functionalized silylamide ligands. Synthesis and crystal structures of [Ni{Me2Si(N-C6H4-2-S-t-Bu)2}], [Ni{Ph2Si(N-C6H4-2-SMe)2}] and [Ni{Ph2Si(N-C6H4-2-SPh)2}]](https://www.degruyter.com/document/doi/10.1515/znb-2018-0263/asset/graphic/j_znb-2018-0263_scheme_001.jpg)
Ni(II) complexes with thioether-functionalized silylamide ligands. Synthesis and crystal structures of [Ni{Me2Si(N-C6H4-2-S-t-Bu)2}], [Ni{Ph2Si(N-C6H4-2-SMe)2}] and [Ni{Ph2Si(N-C6H4-2-SPh)2}]
![SOLVED: 23)Predict the product for each alkylation reaction below: 0 NaNH2 Chgbr 2. CHBr BuLi 2. CHzBr NaNHz NaNHz 2. CH3CHzBr 3. NaNHz PhCHzBr HS=H SOLVED: 23)Predict the product for each alkylation reaction below: 0 NaNH2 Chgbr 2. CHBr BuLi 2. CHzBr NaNHz NaNHz 2. CH3CHzBr 3. NaNHz PhCHzBr HS=H](https://cdn.numerade.com/ask_images/0fc8ceff225643f6bf50958ba32ad1a9.jpg)
SOLVED: 23)Predict the product for each alkylation reaction below: 0 NaNH2 Chgbr 2. CHBr BuLi 2. CHzBr NaNHz NaNHz 2. CH3CHzBr 3. NaNHz PhCHzBr HS=H
![Crystal Structures of n-BuLi Adducts with (R,R)-TMCDA and the Consequences for the Deprotonation of Benzene | Journal of the American Chemical Society Crystal Structures of n-BuLi Adducts with (R,R)-TMCDA and the Consequences for the Deprotonation of Benzene | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja8017187/asset/images/large/ja-2008-017187_0007.jpeg)
Crystal Structures of n-BuLi Adducts with (R,R)-TMCDA and the Consequences for the Deprotonation of Benzene | Journal of the American Chemical Society
![NMR and DFT Studies with a Doubly Labelled 15N/6Li S‐Trifluoromethyl Sulfoximine Reveal Why a Directed ortho‐Lithiation Requires an Excess of n‐ BuLi - Hédouin - Angewandte Chemie International Edition - Wiley Online Library NMR and DFT Studies with a Doubly Labelled 15N/6Li S‐Trifluoromethyl Sulfoximine Reveal Why a Directed ortho‐Lithiation Requires an Excess of n‐ BuLi - Hédouin - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/4aaa0691-61cb-47c0-99a9-f8aa4d87add9/anie202214106-toc-0001-m.jpg)
NMR and DFT Studies with a Doubly Labelled 15N/6Li S‐Trifluoromethyl Sulfoximine Reveal Why a Directed ortho‐Lithiation Requires an Excess of n‐ BuLi - Hédouin - Angewandte Chemie International Edition - Wiley Online Library
![Practical chemical synthesis of FICZ (1). (i) n-BuLi, THF, −70 °C. 77%.... | Download Scientific Diagram Practical chemical synthesis of FICZ (1). (i) n-BuLi, THF, −70 °C. 77%.... | Download Scientific Diagram](https://www.researchgate.net/publication/334371981/figure/fig3/AS:959518448025600@1605778433109/Practical-chemical-synthesis-of-FICZ-1-i-n-BuLi-THF-70C-77-ii-LiAlH4-THF.png)