Diverse reactivity of a magnesium silanide toward ketones

2Citations
Citations of this article
10Readers
Mendeley users who have this article in their library.

Abstract

The reactivity of a molecular magnesium silanide toward ketones displays a significant variability of outcome, resulting in adduct formation, deprotonation, dearomatisation or deoxygenation, that is dependent on the structure and electronic character of the carbonyl-containing reagent.

References Powered by Scopus

Isomerism of Some α-Hydroxysilanes to Silyl Ethers

139Citations
N/AReaders
Get full text

One-electron reduction of aromatic ketones by low-valent lanthanides. Isolation structural characterization, and reactivity of lanthanide ketyl complexes

123Citations
N/AReaders
Get full text

Silicon-Derived Singlet Nucleophilic Carbene Reagents in Organic Synthesis

81Citations
N/AReaders
Get full text

Cited by Powered by Scopus

Heterometallic Mg-Ni-Mg Complex Promoted Hydrosilylation of Alkenes: Catalytic Performance and Intermediates Characterization<sup>†</sup>

3Citations
N/AReaders
Get full text

Reactivity of [Tism<sup>PriBenz</sup>]MgH and [Tism<sup>PriBenz</sup>]MgMe towards Carbonyl Compounds: Access to Terminal Alkoxide and Enolate Complexes

2Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Okokhere-Edeghoghon, B., Hill, M. S., Mahon, M. F., & McMullin, C. L. (2022). Diverse reactivity of a magnesium silanide toward ketones. Chemical Communications, 58(76), 10711–10714. https://doi.org/10.1039/d2cc03966d

Readers over time

‘22‘2302468

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 4

100%

Readers' Discipline

Tooltip

Chemistry 6

100%

Save time finding and organizing research with Mendeley

Sign up for free
0