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The Truce–Smiles rearrangement and related reactions: a review
Author(s) -
Anna Henderson,
Joel R. Kosowan,
Tabitha E. Wood
Publication year - 2017
Publication title -
canadian journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.323
H-Index - 68
eISSN - 1480-3291
pISSN - 0008-4042
DOI - 10.1139/cjc-2016-0594
Subject(s) - smiles rearrangement , chemistry , nucleophilic aromatic substitution , scope (computer science) , intramolecular force , aryl , substrate (aquarium) , rearrangement reaction , nucleophilic substitution , leaving group , computational chemistry , stereochemistry , medicinal chemistry , organic chemistry , computer science , catalysis , programming language , geology , alkyl , oceanography
The Truce–Smiles rearrangement is an X → C aryl migration reaction that is achieved by an intramolecular nucleophilic aromatic substitution pathway. The reaction exhibits a wide substrate scope with respect to a migrating aryl ring and leaving group, appearing in many different tandem reaction sequences, to achieve a wide variety of product outcomes. We present an extensive survey of reported examples of the Truce–Smiles rearrangement from the chemistry literature (1950s until present) organized by various substrate design variables or aspects of the reaction method. Present deficiencies in our understanding of the reaction are identified with recommendations for future research directions and useful developments in the application of the reaction are celebrated.

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