Enantioselective, Noncovalent, Substrate‐Directable Heck–Matsuda and Oxidative Heck Arylations of Unactivated Five‐Membered Carbocyclic Olefins-Reference-Cited by-同舟云学术

Enantioselective, Noncovalent, Substrate‐Directable Heck–Matsuda and Oxidative Heck Arylations of Unactivated Five‐Membered Carbocyclic Olefins

Published:2018-07-12 Issue:45 Volume:24 Page:11738-11747
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

de Oliveira Juliana Manso¹,Angnes Ricardo Almir¹,Khan Ismat Ullah¹²,Polo Ellen Christine¹^ORCID,Heerdt Gabriel¹,Servilha Bruno M.³,Menezes da Silva Vitor H.¹^ORCID,Braga Ataualpa A. C.³,Correia Carlos Roque Duarte¹^ORCID

Affiliation:

1. Department of Organic ChemistryUniversity of Campinas, Chemistry Institute, C.P. 6154 CEP. 13083-970 Campinas São Paulo Brazil

2. Department of ChemistryQuaid-i-Azam University Islamabad 45320 Pakistan

3. Department of Fundamental ChemistryUniversity of São Paulo Avenida Lineu Prestes, 748, Bl. 05 sup. Sl 0552 Butantã São Paulo, SP Brazil

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201801910

Reference85 articles.

2. The Heck Reaction as a Sharpening Stone of Palladium Catalysis

3. Non-conventional methodologies for transition-metal catalysed carbon–carbon coupling: a critical overview. Part 1: The Heck reaction

4. Diazonium Salts as Substrates in Palladium-Catalyzed Cross-Coupling Reactions

5. Evolution and Synthetic Applications of the Heck–Matsuda Reaction: The Return of Arenediazonium Salts to Prominence

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