Articles with "brook rearrangement" as a keyword



Photo from archive.org

Isolable endocyclic silenes by thermal Brook rearrangement

Sign Up to like & get
recommendations!
Published in 2017 at "Journal of Organometallic Chemistry"

DOI: 10.1016/j.jorganchem.2016.12.019

Abstract: Abstract In the following study, we investigated thermally and photolytically induced transformations of acylcyclotetrasilanes (Me3Si)2Si4Me8(Me3Si)COR (compounds 9a-c; R = alkyl, aryl). Mild thermolysis of 9a-c below 130 °C cleanly and selectively afforded the corresponding endocyclic silenes 10b-d irrespective… read more here.

Keywords: thermal brook; silenes thermal; endocyclic silenes; brook rearrangement ... See more keywords

Cation Bridge Mediating Homo- and Cross-Coupling in Copper-Catalyzed Reductive Coupling of Benzaldehyde and Benzophenone.

Sign Up to like & get
recommendations!
Published in 2022 at "Inorganic chemistry"

DOI: 10.1021/acs.inorgchem.2c02392

Abstract: A novel mechanism of organobase-mediated Brook rearrangement and C-C coupling in the copper-catalyzed reductive coupling of benzaldehyde and benzophenone is proposed. The results demonstrate that this reaction proceeds mainly through five sequential elementary steps: transmetalation,… read more here.

Keywords: coupling copper; reductive coupling; coupling benzaldehyde; brook rearrangement ... See more keywords

Umpolung Phosphorylation of Tyrosine via 1,2-Phospha-Brook Rearrangement.

Sign Up to like & get
recommendations!
Published in 2024 at "Organic letters"

DOI: 10.1021/acs.orglett.4c03223

Abstract: Phosphorylated tyrosine is a fundamental building block of bioactive peptides and proteins. However, the chemoselective phosphorylation of tyrosine over other nucleophilic amino acid residues in unprotected peptides remains a significant challenge. Here we report an… read more here.

Keywords: brook rearrangement; phospha brook; phosphorylation tyrosine; tyrosine ... See more keywords

Asymmetric retro-[1,4]-Brook rearrangement of 3-silyl allyloxysilanes via chirality transfer from silicon to carbon

Sign Up to like & get
recommendations!
Published in 2019 at "RSC Advances"

DOI: 10.1039/c9ra05482k

Abstract: Asymmetric retro-[1,4]-Brook rearrangement of 3-silyl allyloxysilanes has been developed involving Si-to-C chirality transfer, which is diastereoselective without loss of enantiomeric excess. read more here.

Keywords: chirality transfer; rearrangement silyl; asymmetric retro; brook rearrangement ... See more keywords