Simple preparation of aryltributylstannanes and its application to one-pot synthesis of diaryl ketones

doi:10.1016/J.TET.2015.01.048

Paper

Simple preparation of aryltributylstannanes and its application to one-pot synthesis of diaryl ketones

Published Mar 18, 2015 · Asuka Oikawa, Gan Kindaichi, Yasutaka Shimotori

Tetrahedron

Q3 SJR score

11

Citations

0

Influential Citations

Full textSemantic Scholar

Abstract

Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.

Study Snapshot

Aryltributylstannanes can be prepared by treating arylboronic acids with tributyltin methoxide at 100°C for 1 hour, enabling one-pot synthesis of diaryl ketones in good to high yields.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Sign up to use Study Snapshot

Consensus is limited without an account. Create an account or sign in to get more searches and use the Study Snapshot.

Create an account

Paper

Simple preparation of aryltributylstannanes and its application to one-pot synthesis of diaryl ketones

Sign up to use Study Snapshot

References

Citations

A new and the first metal organic framework for the synthesis of aryl ketones via carbonyl‐Heck cross‐coupling reaction of aryl halides and aldehydes

Co-TIST is a new metal organic framework that effectively catalyzes the carbonyl-Heck cross-coupling reaction, resulting in high yields of aryl ketones without high temperature or additives.

Synthesis and structure-activity relationship study of phenoxybenzylpiperazine analogues as CCR8 agonists

Phenoxybenzylpiperazine analogues with various linkers and small substituents show promising CCR8 agonistic potency, with the most potent congener being 10-fold more potent than ZK756326.

Copper(I)-Mediated 11C-Carboxylation of (Hetero)arylstannanes

Copper(I)-mediated 11C-carboxylation of (hetero)arylstannanes is a mild, radiosynthetic approach for carbon-11-labeled aromatic and heteroaromatic carboxylic acids, with potential applications in radiosynthesis of retinoid X receptor agonist

[1,2,5]Thiadiazolo[3,4-d]Pyridazine as an Internal Acceptor in the D-A-π-A Organic Sensitizers for Dye-Sensitized Solar Cells

New D-A--A metal-free organic sensitizers for dye-sensitized solar cells show potential for further optimization, with the donor attached to the internal acceptor not playing an essential role in photovoltaic properties.

Synthesis of the 4,7-Dibromo Derivative of Highly Electron-Deficient [1,2,5]Thiadiazolo[3,4-d ]pyridazine and Its Cross-Coupling Reactions

The efficient synthesis of 4,7-dibromo[1,2,5]thiadiazolo[3,4-d]pyridazine and its cross-coupling reactions enable the selective formation of various mono- and diarylated derivatives of strongly electron-accepting heterocycles.