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Predicting Catalyst Extrudate Breakage Based on the Modulus of Rupture
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Catalyst-controlled positional-selectivity in C-H functionalizations.

Virendra Kumar Tiwari1, Manmohan Kapur

  • 1Department of Chemistry, Indian Institute of Science Education and Research Bhopal, Bhopal Bypass Road, Bhopal 462066, MP, India. mk@iiserb.ac.in.

Organic & Biomolecular Chemistry
|January 3, 2019
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Summary
This summary is machine-generated.

Chemists can now control which C-H bond reacts using specific catalysts. This review explores methods for switching site-selectivity in C-H functionalization for targeted organic synthesis.

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Area of Science:

  • Organic Chemistry
  • Catalysis

Background:

  • C-H bonds are abundant but typically chemically identical.
  • Selective functionalization of specific C-H bonds is a major synthetic challenge.
  • Transition metal-catalyzed C-H functionalization offers new synthetic possibilities.

Purpose of the Study:

  • To review strategies for controlling positional selectivity in C-H bond functionalization.
  • To discuss how catalytic systems can be altered to switch regioselectivity.
  • To highlight the impact of regiodivergent C-H functionalization on synthetic chemistry.

Main Methods:

  • Focuses on reviewing existing literature on catalytic systems.
  • Analyzes different mechanistic approaches to C-H activation.
  • Examines how catalyst choice influences site-selectivity.

Main Results:

  • Recent advances enable regiodivergent C-H functionalization.
  • Switching regioselectivity between reactive sites is achievable via catalytic control.
  • Altering catalytic systems can redirect C-H functionalization to different sites.

Conclusions:

  • Controlled, positional-selective C-H bond functionalization is a key goal in organic synthesis.
  • Catalytic system modification is crucial for achieving switchable site-selectivity.
  • This review provides insights into manipulating catalysts for targeted C-H activation.