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ACS Central Science
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October 6, 2017
Alkene Photo-Isomerization Inspired by Vision
Colin M Pearson, Thomas N Snaddon
Organic & Biomolecular Chemistry
|
December 17, 2005
Highly efficient methods for the one-pot synthesis of beta-substituted enones
William J Kerr, Colin M Pearson, Graeme J Thurston
Angewandte Chemie (International Ed. in English)
|
May 28, 2019
A Regio- and Stereodivergent Synthesis of Homoallylic Amines by a One-Pot Cooperative-Catalysis-Based Allylic Alkylation/Hofmann Rearrangement Strategy
Colin M Pearson, James W B Fyfe, Thomas N Snaddon
Organic & Biomolecular Chemistry
|
June 25, 2005
New odourless protocols for efficient Pauson-Khand annulations
Jack A Brown, Stephanie Irvine, William J Kerr, et al.
Topics in Current Chemistry (Cham)
|
January 17, 2020
Tertiary Amine Lewis Base Catalysis in Combination with Transition Metal Catalysis
Gary J Knox, Luke S Hutchings-Goetz, Colin M Pearson, et al.
Organic Letters
|
June 12, 2019
A Modular Construction of Epidithiodiketopiperazines
Thomas N Snaddon, Toya D Scaggs, Colin M Pearson, et al.
Tetrahedron
|
December 19, 2018
Si-Directed regiocontrol in asymmetric Pd-catalyzed allylic alkylations using C1-ammonium enolate nucleophiles
James W B Fyfe, Omaru M Kabia, Colin M Pearson, et al.
Angewandte Chemie (International Ed. in English)
|
April 28, 2018
Traversing Steric Limitations by Cooperative Lewis Base/Palladium Catalysis: An Enantioselective Synthesis of α-Branched Esters Using 2-Substituted Allyl Electrophiles
Kevin J Schwarz, Colin M Pearson, Gabriel A Cintron-Rosado, et al.
Angewandte Chemie (International Ed. in English)
|
August 24, 2012
Convergent total syntheses of callipeltosides A, B, and C
James R Frost, Colin M Pearson, Thomas N Snaddon, et al.
Angewandte Chemie (International Ed. in English)
|
March 21, 2022
A Pd-H/Isothiourea Cooperative Catalysis Approach to anti-Aldol Motifs: Enantioselective α-Alkylation of Esters with Oxyallenes
Hua-Chen Lin, Gary J Knox, Colin M Pearson, et al.
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Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
ACS Central Science
|
October 6, 2017
Alkene Photo-Isomerization Inspired by Vision
Colin M Pearson, Thomas N Snaddon
Organic & Biomolecular Chemistry
|
December 17, 2005
Highly efficient methods for the one-pot synthesis of beta-substituted enones
William J Kerr, Colin M Pearson, Graeme J Thurston
Angewandte Chemie (International Ed. in English)
|
May 28, 2019
A Regio- and Stereodivergent Synthesis of Homoallylic Amines by a One-Pot Cooperative-Catalysis-Based Allylic Alkylation/Hofmann Rearrangement Strategy
Colin M Pearson, James W B Fyfe, Thomas N Snaddon
Organic & Biomolecular Chemistry
|
June 25, 2005
New odourless protocols for efficient Pauson-Khand annulations
Jack A Brown, Stephanie Irvine, William J Kerr, et al.
Topics in Current Chemistry (Cham)
|
January 17, 2020
Tertiary Amine Lewis Base Catalysis in Combination with Transition Metal Catalysis
Gary J Knox, Luke S Hutchings-Goetz, Colin M Pearson, et al.
Organic Letters
|
June 12, 2019
A Modular Construction of Epidithiodiketopiperazines
Thomas N Snaddon, Toya D Scaggs, Colin M Pearson, et al.
Tetrahedron
|
December 19, 2018
Si-Directed regiocontrol in asymmetric Pd-catalyzed allylic alkylations using C1-ammonium enolate nucleophiles
James W B Fyfe, Omaru M Kabia, Colin M Pearson, et al.
Angewandte Chemie (International Ed. in English)
|
April 28, 2018
Traversing Steric Limitations by Cooperative Lewis Base/Palladium Catalysis: An Enantioselective Synthesis of α-Branched Esters Using 2-Substituted Allyl Electrophiles
Kevin J Schwarz, Colin M Pearson, Gabriel A Cintron-Rosado, et al.
Angewandte Chemie (International Ed. in English)
|
August 24, 2012
Convergent total syntheses of callipeltosides A, B, and C
James R Frost, Colin M Pearson, Thomas N Snaddon, et al.
Angewandte Chemie (International Ed. in English)
|
March 21, 2022
A Pd-H/Isothiourea Cooperative Catalysis Approach to anti-Aldol Motifs: Enantioselective α-Alkylation of Esters with Oxyallenes
Hua-Chen Lin, Gary J Knox, Colin M Pearson, et al.
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of 2