Synthesis 2016; 48(06): 804-815
DOI: 10.1055/s-0035-1561321
short review
© Georg Thieme Verlag Stuttgart · New York

Palladium-Catalyzed Olefination of Aryl C–H Bonds by Using Directing­ Scaffolds

Sukdev Bag
Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India   Email: dmaiti@chem.iitb.ac.in
,
Debabrata Maiti*
Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India   Email: dmaiti@chem.iitb.ac.in
› Author Affiliations
Further Information

Publication History

Received: 03 November 2015

Accepted after revision: 15 December 2015

Publication Date:
26 January 2016 (online)


Abstract

Site selective C–H bond activation/C–C bond formation is an ideal target for organic chemists owing to the ubiquitous nature of C–H bonds in natural products. A particular aryl C–H bond can be predictably activated by a directing group. However, the majority of strong and weak coordinating directing groups have been implemented for ortho­-C–H bond activation/C-alkenylation. More recently, meta-C–H functionalization has been promoted by fine-tuning directing templates. In this short review, we have summarized recent progress in palladium-catalyzed directing group/template-assisted ortho/meta-C–H olefination.

1 Introduction

2 Proximal C–H Olefination

3 Distal C–H Olefination

4 Conclusions

 
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