Ortho Palladation of the Phenethylamines of Biological Relevance l-Tyrosine Methyl Ester and Homoveratrylamine. Reactivity of the Palladacycles toward CO and Isocyanides. Synthesis of the Natural Alkaloid Corydaldine-Reference-Cited by-同舟云学术

Ortho Palladation of the Phenethylamines of Biological Relevance l-Tyrosine Methyl Ester and Homoveratrylamine. Reactivity of the Palladacycles toward CO and Isocyanides. Synthesis of the Natural Alkaloid Corydaldine

Published:2012-04-12 Issue:9 Volume:31 Page:3647-3660
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Oliva-Madrid María-José¹,Garcı́a-López José-Antonio¹,Saura-Llamas Isabel¹,Bautista Delia¹,Vicente José¹

Affiliation:

1. Grupo de Química Organometálica, Departamento de Química Inorgánica, Facultad de Química, and ‡SAI, Universidad de Murcia, Apartado 4021, E-30071 Murcia, Spain

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om300141b

Reference93 articles.

1. Application of palladacycles in Heck type reactions

2. Cyclometalated Phosphine-Based Pincer Complexes: Mechanistic Insight in Catalysis, Coordination, and Bond Activation

3. Palladacycles in catalysis – a critical survey

4. Oxime-derived palladacycles as source of palladium nanoparticles

5. The Potential of Palladacycles: More Than Just Precatalysts

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