Ynamide Carbopalladation: A Flexible Route to Mono‐, Bi‐ and Tricyclic Azacycles-Reference-Cited by-同舟云学术

Ynamide Carbopalladation: A Flexible Route to Mono‐, Bi‐ and Tricyclic Azacycles

Published:2015-07-16 Issue:36 Volume:21 Page:12627-12639
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Campbell Craig D.¹,Greenaway Rebecca L.¹,Holton Oliver T.¹,Walker P. Ross¹,Chapman Helen A.²,Russell C. Adam²,Carr Greg³,Thomson Amber L.¹,Anderson Edward A.¹

Affiliation:

1. Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford, OX1 3TA (U.K.) edward.

2. Syngenta Ltd. Jealott's Hill International Research Centre, Bracknell, Berkshire, RG42 6EY (U.K.)

3. AstraZeneca, Alderley Park, Macclesfield, SK10 4TF (U.K.)

Funder

Funded Access

EPSRC

Syngenta

AstraZeneca

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201501710

Reference159 articles.

2. An overview of the key routes to the best selling 5-membered ring heterocyclic pharmaceuticals

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4. For recent reviews of ynamide chemistry see:

5. Designing Enzyme-like Catalysts: A Rhodium(II) Metallopeptide Case Study

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