Beatrice Collins

Affiliations: 
2009-2013 Chemistry University of Cambridge, Cambridge, England, United Kingdom 
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"Beatrice Collins"
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Parents

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Matthew Gaunt grad student 2009-2013 Cambridge
Bernard L. Feringa post-doc 2013-2015 RUG
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Publications

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Watts OFB, Berreur J, Collins BSL, et al. (2022) Biocatalytic Enantioselective Synthesis of Atropisomers. Accounts of Chemical Research
Rubial B, Collins BSL, Bigler R, et al. (2018) Enantiospecific Synthesis of ortho-Substituted 1,1-Diarylalkanes by a 1,2-Metalate Rearrangement/anti-SN2' Elimination/Rearomatizing Allylic Suzuki-Miyaura Reaction Sequence. Angewandte Chemie (International Ed. in English)
Vlatković M, Volarić J, Collins BSL, et al. (2017) Dynamic control over catalytic function using responsive bisthiourea catalysts. Organic & Biomolecular Chemistry
Aggarwal VK, Collins B, Wilson C, et al. (2017) Asymmetric Synthesis of Secondary and Tertiary Boronic Esters. Angewandte Chemie (International Ed. in English)
Pizzolato SF, Collins BS, van Leeuwen T, et al. (2016) Bifunctional Molecular Photoswitches based on Overcrowded Alkenes for Dynamic Control of Catalytic Activity in Michael Addition Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany)
Collins BSL, Kistemaker JCM, Otten E, et al. (2016) A chemically powered unidirectional rotary molecular motor based on a palladium redox cycle Nature Chemistry. 8: 860-866
McNally A, Haffemayer B, Collins BS, et al. (2014) Palladium-catalysed C-H activation of aliphatic amines to give strained nitrogen heterocycles. Nature. 510: 129-33
McNally A, Haffemayer B, Collins BSL, et al. (2014) Correction: Corrigendum: Palladium-catalysed C–H activation of aliphatic amines to give strained nitrogen heterocycles Nature. 512: 338-338
Collins BS, Suero MG, Gaunt MJ. (2013) Copper-catalyzed arylative Meyer-Schuster rearrangement of propargylic alcohols to complex enones using diaryliodonium salts. Angewandte Chemie (International Ed. in English). 52: 5799-802
Suero MG, Bayle ED, Collins BS, et al. (2013) Copper-catalyzed electrophilic carbofunctionalization of alkynes to highly functionalized tetrasubstituted alkenes. Journal of the American Chemical Society. 135: 5332-5
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