Iron-Catalyzed Deoxygenative Diborylation of Ketones to Internal gem-Diboronates
- Corresponding author: Liu Chao, chaoliu@licp.cas.cn
Citation:
He Zeyu, Fan Min, Xu Jia'neng, Hu Yue, Wang Lu, Wu Xudong, Xia Chungu, Liu Chao. Iron-Catalyzed Deoxygenative Diborylation of Ketones to Internal gem-Diboronates[J]. Chinese Journal of Organic Chemistry,
;2019, 39(12): 3438-3445.
doi:
10.6023/cjoc201909008
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Conditions and regents: 1s (10.0 mmol), B2pin2 (2.8 equiv. 28.0 mmol), NaOtBu (1.3 equiv. 13.0 mmol), FeBr2 (10 mol%, 1.0 mmol), toluene (50.0 mL), 100 ℃ for 5 h in N2 atmosphere. Yields are based on isolated products
Reaction conditions: (a) 2wa (0.39 mmol), 1-bromoocatane (0.3 mmol), NaOtBu (0.9 mmol), THF, r.t., 12 h; (b) 2wa (0.375 mmol), MeLi (0.625 mmol, 1.6 mol/L in diethyl ether), benzoic acid (0.25 mmol), methyl bromoacetate (0.5 mmol), THF; (c) 2-bromothiophene (0.36 mmol), nBuLi (0.36 mmol, 1.6 mol/L in hexanes), 3a (0.3 mmol), NBS (0.36 mmol), THF.