Recent Advances in Transition-Metal-Catalyzed Selective Synthesis of π‑Conjugated Silacycles: A Mini-Review
Syed Soil Jabed Ali1, Rudra Shankar Das1, Sandeep Kumar2
1Department of Chemistry, Sister Nivedita University DG Block, Action Area 1, New Town, West Bengal 700156, India.
Abstract:
Although the synthesis of silacycles is of significant importance, it remains far less explored than that of N-, O-, and S-heterocycles. The past few years have seen growing attention toward the synthesis of these silacycles, owing to their applications in light-emitting materials, thin-film transistors, electroluminescent devices, solar cells, and notable photophysical and biological activities. In this review, we have discussed the recent developments in transition-metal-catalyzed synthesis of π-conjugated silacycles by C-H activation, 1,n-metal migration and cycloaddition reactions, chemo- and regio-divergent reactions, coupling reactions, and β-hydride eliminations. The discussion of the key components of each strategy, with mechanistic study and the role of phosphine ligands are outlined with key achievements, limitations, and major applications.
More Related Videos
09:45Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
Published on: March 20, 2017
07:50Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides
Published on: May 26, 2019
Related Concept Videos
Cycloaddition Reactions: Overview
Diels–Alder Reaction Forming Cyclic Products: Stereochemistry
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction
