4.5 Article

Highly Selective Hydroxylation and Alkoxylation of Silanes: One-Pot Silane Oxidation and Reduction of Aldehydes/Ketones

期刊

ORGANOMETALLICS
卷 39, 期 1, 页码 165-171

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AMER CHEMICAL SOC
DOI: 10.1021/acs.organomet.9b00716

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资金

  1. National Natural Science Foundation of China [21962004, 21961002, 21562004]
  2. Jiangxi Education Hall Science and Technology Foundation [GJJ180801, GJJ170867, GJJ150944]
  3. Jiangxi provincial department of science and technology [20192BAB203004, 20161BAB213059]
  4. Fundamental Research Funds for Gannan Medical University [PY201301, QD201810, QD201816, QD201832]

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An efficient chemoselective iridium-catalyzed method for the hydroxylation and alkoxylation of organosilanes to generate hydrogen gas and silanols or silyl ethers was developed. A variety of sterically hindered silanes with alkyl, aryl, and ether groups were tolerated. Furthermore, this atom-economical catalytic protocol can be used for the synthesis of silanediols and silanetriols. A one-pot silane oxidation and chemoselective reduction of aldehydes/ketones was also realized.

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