Abstract
Organosilanes have secured a special place in the synthetic world for several decades. However, among them, allylsilanes are a choice reagent for organic chemists to develop novel organic transformations. In recent years researchers have proved that visible-light photoredox catalysis has emerged as one of the most mild, sustainable, straightforward, and efficient strategies to construct simple to complex molecules with or without enantioselectivity. This review provides an in-depth analysis of recent advances and strategies employed in visible-light photoredox catalysis for allylsilane and its analogues for the development of various organic transformations. The review is divided into sections, each focused on a specific reactivity of allylsilane under light irradiation with C(sp2) center arene or alkene, C(sp2) center carbonyl, and C(sp3) center carbon functionality. In this review, we present optimization data, reaction scope, and mechanistic aspects to bring forward specific reactivity and selectivity trends of allylsilane in photoredox conditions.
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