Enantioselective Oxy-Heck-Matsuda Arylations: Expeditious Synthesis of Dihydrobenzofuran Systems and Total Synthesis of the Neolignan (−)-Conocarpan-Reference-Cited by-同舟云学术

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Enantioselective Oxy-Heck-Matsuda Arylations: Expeditious Synthesis of Dihydrobenzofuran Systems and Total Synthesis of the Neolignan (−)-Conocarpan

Published:2018-01-11 Issue:2 Volume:360 Page:346-365
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Silva Allan R.¹,Polo Ellen C.¹,Martins Nelson C.¹,Correia Carlos Roque D.¹

Affiliation:

1. Institute of Chemistry; University of Campinas, UNICAMP, Campinas; São Paulo Brazil

Funder

São Paulo Research Foundation

Brazilian National Research Council

CNPq

Coordination for the Improvement of Higher Education Personnel (PNPD-CAPES)

Publisher

Wiley

Subject

General Chemistry

Reference84 articles.

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

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

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

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

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