Year |
Citation |
Score |
2018 |
Rubial B, Collins BSL, Bigler R, Aichhorn S, Noble A, Aggarwal VK. 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). PMID 30520228 DOI: 10.1002/Anie.201811343 |
0.322 |
|
2017 |
Vlatković M, Volarić J, Collins BSL, Bernardi L, Feringa BL. Dynamic control over catalytic function using responsive bisthiourea catalysts. Organic & Biomolecular Chemistry. PMID 28858354 DOI: 10.1039/C7Ob01851G |
0.403 |
|
2016 |
Collins BSL, Kistemaker JCM, Otten E, Feringa BL. A chemically powered unidirectional rotary molecular motor based on a palladium redox cycle Nature Chemistry. 8: 860-866. DOI: 10.1038/Nchem.2543 |
0.306 |
|
2014 |
McNally A, Haffemayer B, Collins BS, Gaunt MJ. Palladium-catalysed C-H activation of aliphatic amines to give strained nitrogen heterocycles. Nature. 510: 129-33. PMID 24870240 DOI: 10.1038/nature13389 |
0.587 |
|
2014 |
McNally A, Haffemayer B, Collins BSL, Gaunt MJ. Correction: Corrigendum: Palladium-catalysed C–H activation of aliphatic amines to give strained nitrogen heterocycles Nature. 512: 338-338. DOI: 10.1038/nature13635 |
0.561 |
|
2013 |
Collins BS, Suero MG, Gaunt MJ. Copper-catalyzed arylative Meyer-Schuster rearrangement of propargylic alcohols to complex enones using diaryliodonium salts. Angewandte Chemie (International Ed. in English). 52: 5799-802. PMID 23610012 DOI: 10.1002/anie.201301529 |
0.595 |
|
2013 |
Suero MG, Bayle ED, Collins BS, Gaunt MJ. Copper-catalyzed electrophilic carbofunctionalization of alkynes to highly functionalized tetrasubstituted alkenes. Journal of the American Chemical Society. 135: 5332-5. PMID 23521626 DOI: 10.1021/ja401840j |
0.566 |
|
2011 |
Tredwell MJ, Gulias M, Bremeyer NG, Johansson CC, Collins BS, Gaunt MJ. Palladium(II)-catalyzed C-H bond arylation of electron-deficient arenes at room temperature. Angewandte Chemie (International Ed. in English). 50: 1076-9. PMID 21268198 DOI: 10.1002/Anie.201005990 |
0.52 |
|
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