Acylsilanes and their applications in organic chemistry
有机人名反应（34）：Brook rearrangement - YouTube
![Scope of [1,5]-Brook rearrangement-addition of 1a with electrophiles | Download Table](https://www.researchgate.net/profile/Yin-Zhiping/publication/256074270/figure/tbl2/AS:601786859671557@1520488576205/Scope-of-1-5-Brook-rearrangement-addition-of-1a-with-electrophiles_Q640.jpg "Scope of [1,5]-Brook rearrangement-addition of 1a with electrophiles | Download Table")
Scope of [1,5]-Brook rearrangement-addition of 1a with electrophiles | Download Table
Acylsilanes and their applications in organic chemistry
![1,5]-Brook rearrangement: an overlooked but valuable silyl migration to synthesize configurationally defined vinylsilane. The unique steric and electronic effects of geminal bis(silane) - Chemical Communications (RSC Publishing)](https://pubs.rsc.org/image/article/2013/cc/c3cc45002c/c3cc45002c-s1.gif "1,5]-Brook rearrangement: an overlooked but valuable silyl migration to synthesize configurationally defined vinylsilane. The unique steric and electronic effects of geminal bis(silane) - Chemical Communications (RSC Publishing)")
1,5]-Brook rearrangement: an overlooked but valuable silyl migration to synthesize configurationally defined vinylsilane. The unique steric and electronic effects of geminal bis(silane) - Chemical Communications (RSC Publishing)
Brook Silaketone Rearrangement - an overview | ScienceDirect Topics
UGI Reaction & Brook rearrangement
Brook rearrangement
![Asymmetric retro-[1,4]-Brook rearrangement of 3-silyl allyloxysilanes via chirality transfer from silicon to carbon - RSC Advances (RSC Publishing)](https://pubs.rsc.org/image/article/2019/ra/c9ra05482k/c9ra05482k-s1_hi-res.gif "Asymmetric retro-[1,4]-Brook rearrangement of 3-silyl allyloxysilanes via chirality transfer from silicon to carbon - RSC Advances (RSC Publishing)")
Asymmetric retro-[1,4]-Brook rearrangement of 3-silyl allyloxysilanes via chirality transfer from silicon to carbon - RSC Advances (RSC Publishing)
Brook Silaketone Rearrangement - an overview | ScienceDirect Topics
Acylsilanes and their applications in organic chemistry
Regioselective lithiation/retro-Brook rearrangement via direct deprotonation - ScienceDirect
Brook rearrangement
Rearrangement
![Asymmetric retro-[1,4]-Brook rearrangement of 3-silyl allyloxysilanes via chirality transfer from silicon to carbon - RSC Advances (RSC Publishing)](https://pubs.rsc.org/image/article/2019/ra/c9ra05482k/c9ra05482k-s2_hi-res.gif "Asymmetric retro-[1,4]-Brook rearrangement of 3-silyl allyloxysilanes via chirality transfer from silicon to carbon - RSC Advances (RSC Publishing)")
Asymmetric retro-[1,4]-Brook rearrangement of 3-silyl allyloxysilanes via chirality transfer from silicon to carbon - RSC Advances (RSC Publishing)
![Mechanistic investigation on N → Cα → O relay via non-Brook rearrangement: reaction conditions promote synthesis of furo[3,2-c]pyridinones - Organic & Biomolecular Chemistry (RSC Publishing)](https://pubs.rsc.org/en/Content/Image/GA/C7OB02081C "Mechanistic investigation on N → Cα → O relay via non-Brook rearrangement: reaction conditions promote synthesis of furo[3,2-c]pyridinones - Organic & Biomolecular Chemistry (RSC Publishing)")
Mechanistic investigation on N → Cα → O relay via non-Brook rearrangement: reaction conditions promote synthesis of furo[3,2-c]pyridinones - Organic & Biomolecular Chemistry (RSC Publishing)
Rearrangement
Retro‐Brook Rearrangement of Ferrocene‐Derived Silyl Ethers,Chemistry - A European Journal - X-MOL
Brook Rearrangement
![Oxidative [1,2]-Brook Rearrangements Exploiting Single-Electron Transfer: Photoredox-Catalyzed Alkylations and Arylations. - Abstract - Europe PMC](https://europepmc.org/articles/PMC5575796/bin/nihms898912f1.jpg "Oxidative [1,2]-Brook Rearrangements Exploiting Single-Electron Transfer: Photoredox-Catalyzed Alkylations and Arylations. - Abstract - Europe PMC")
Oxidative [1,2]-Brook Rearrangements Exploiting Single-Electron Transfer: Photoredox-Catalyzed Alkylations and Arylations. - Abstract - Europe PMC
Rearrangement
Brook rearrangement - Wikipedia
Brook rearrangement
Novel sequential 1,4-Brook rearrangement–Wittig reaction: new one-pot approach for silyl dienol ethers - ScienceDirect
![Oxidative [1,2]-Brook Rearrangements Exploiting Single-Electron Transfer: Photoredox-Catalyzed Alkylations and Arylations. - Abstract - Europe PMC](https://europepmc.org/articles/PMC5575796/bin/nihms898912f3.jpg "Oxidative [1,2]-Brook Rearrangements Exploiting Single-Electron Transfer: Photoredox-Catalyzed Alkylations and Arylations. - Abstract - Europe PMC")
Oxidative [1,2]-Brook Rearrangements Exploiting Single-Electron Transfer: Photoredox-Catalyzed Alkylations and Arylations. - Abstract - Europe PMC
![Asymmetric retro-[1,4]-Brook rearrangement of 3-silyl allyloxysilanes via chirality transfer from silicon to carbon - RSC Advances (RSC Publishing)](https://pubs.rsc.org/image/article/2019/ra/c9ra05482k/c9ra05482k-u1_hi-res.gif "Asymmetric retro-[1,4]-Brook rearrangement of 3-silyl allyloxysilanes via chirality transfer from silicon to carbon - RSC Advances (RSC Publishing)")
Asymmetric retro-[1,4]-Brook rearrangement of 3-silyl allyloxysilanes via chirality transfer from silicon to carbon - RSC Advances (RSC Publishing)
