Grant A McGonagle - JoVE Visualize

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The Journal of Organic Chemistry|July 26, 2014

Preparation of amino-substituted indenes and 1,4-dihydronaphthalenes using a one-pot multireaction approach: total synthesis of oxybenzo[c]phenanthridine alkaloidsEwen D D Calder, Fiona I McGonagle, Alexander H Harkiss, et al.

Bioorganic & Medicinal Chemistry Letters|March 19, 2020

Selective CDK6 degradation mediated by cereblon, VHL, and novel IAP-recruiting PROTACsNiall A Anderson, Jenni Cryan, Adil Ahmed, et al.

ACS Medicinal Chemistry Letters|July 18, 2019

Targeting IRAK4 for Degradation with PROTACsJoao Nunes, Grant A McGonagle, Jessica Eden, et al.

Journal of Medicinal Chemistry|September 13, 2021

Discovery of GSK251: A Highly Potent, Highly Selective, Orally Bioavailable Inhibitor of PI3Kδ with a Novel Binding ModeKenneth Down, Augustin Amour, Niall A Anderson, et al.

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Showing results (1-10 of 4) with videos related to

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Pageof 1

The Journal of Organic Chemistry|July 26, 2014

Preparation of amino-substituted indenes and 1,4-dihydronaphthalenes using a one-pot multireaction approach: total synthesis of oxybenzo[c]phenanthridine alkaloidsEwen D D Calder, Fiona I McGonagle, Alexander H Harkiss, et al.

Bioorganic & Medicinal Chemistry Letters|March 19, 2020

Selective CDK6 degradation mediated by cereblon, VHL, and novel IAP-recruiting PROTACsNiall A Anderson, Jenni Cryan, Adil Ahmed, et al.

ACS Medicinal Chemistry Letters|July 18, 2019

Targeting IRAK4 for Degradation with PROTACsJoao Nunes, Grant A McGonagle, Jessica Eden, et al.

Journal of Medicinal Chemistry|September 13, 2021

Discovery of GSK251: A Highly Potent, Highly Selective, Orally Bioavailable Inhibitor of PI3Kδ with a Novel Binding ModeKenneth Down, Augustin Amour, Niall A Anderson, et al.

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