Year |
Citation |
Score |
2023 |
Solà J, Riera A, Verdaguer X, Maestro MA. Phosphine-Substrate Recognition through the C─H···O Hydrogen Bond: Application to the Asymmetric Pauson-Khand Reaction [ , , 13629-13633]. Journal of the American Chemical Society. 128: 13312. PMID 37908050 DOI: 10.1021/ja066395p |
0.568 |
|
2022 |
Sors-Vendrell A, Ortiz A, Meneses D, Alfonso I, Solà J, Jimeno C. A Degenerate Metal-Templated Catalytic System with Redundant Functional Groups for the Asymmetric Aldol Reaction. The Journal of Organic Chemistry. 87: 7509-7513. PMID 35583468 DOI: 10.1021/acs.joc.2c00414 |
0.654 |
|
2020 |
Solà J, Jimeno C, Alfonso I. Exploiting complexity to implement function in chemical systems. Chemical Communications (Cambridge, England). PMID 32975545 DOI: 10.1039/D0Cc04170J |
0.637 |
|
2019 |
Serra-Pont A, Alfonso I, Solà J, Jimeno C. An efficient dynamic asymmetric catalytic system within a zinc-templated network. Chemical Communications (Cambridge, England). PMID 31219483 DOI: 10.1039/c9cc03958a |
0.627 |
|
2017 |
Serra-Pont A, Alfonso I, Solà J, Jimeno C. A copper-templated, bifunctional organocatalyst: a strongly cooperative dynamic system for the aldol reaction. Organic & Biomolecular Chemistry. PMID 28749514 DOI: 10.1039/c7ob01370a |
0.662 |
|
2016 |
Wilson MR, Solà J, Carlone A, Goldup SM, Lebrasseur N, Leigh DA. An autonomous chemically fuelled small-molecule motor. Nature. 534: 235-40. PMID 27279219 DOI: 10.1038/Nature18013 |
0.507 |
|
2016 |
Kassem S, Lee AT, Leigh DA, Markevicius A, Solà J. Pick-up, transport and release of a molecular cargo using a small-molecule robotic arm. Nature Chemistry. 8: 138-43. PMID 26791896 DOI: 10.1038/Nchem.2410 |
0.63 |
|
2015 |
Serra-Pont A, Alfonso I, Jimeno C, Solà J. Dynamic assembly of a zinc-templated bifunctional organocatalyst in the presence of water for the asymmetric aldol reaction. Chemical Communications (Cambridge, England). PMID 26478115 DOI: 10.1039/C5Cc07847D |
0.668 |
|
2015 |
Byrne L, Solà J, Clayden J. Screw sense alone can govern enantioselective extension of a helical peptide by kinetic resolution of a racemic amino acid. Chemical Communications (Cambridge, England). 51: 10965-8. PMID 26062815 DOI: 10.1039/C5Cc01790D |
0.57 |
|
2014 |
De Poli M, Byrne L, Brown RA, Solà J, Castellanos A, Boddaert T, Wechsel R, Beadle JD, Clayden J. Engineering the structure of an N-terminal β-turn to maximize screw-sense preference in achiral helical peptide chains. The Journal of Organic Chemistry. 79: 4659-75. PMID 24708302 DOI: 10.1021/Jo500714B |
0.733 |
|
2014 |
De Poli M, Byrne L, Brown RA, Solà J, Castellanos A, Boddaert T, Wechsel R, Beadle JD, Clayden J. Engineering the structure of an N-terminal β-turn to maximize screw-sense preference in achiral helical peptide chains. The Journal of Organic Chemistry. 79: 4659-75. PMID 24708302 DOI: 10.1021/Jo500714B |
0.733 |
|
2014 |
Byrne L, Solà J, Boddaert T, Marcelli T, Adams RW, Morris GA, Clayden J. Foldamer-mediated remote stereocontrol: >1,60 asymmetric induction. Angewandte Chemie (International Ed. in English). 53: 151-5. PMID 24375739 DOI: 10.1002/Anie.201308264 |
0.755 |
|
2012 |
Boddaert T, Solà J, Helliwell M, Clayden J. Chemical communication: conductors and insulators of screw-sense preference between helical oligo(aminoisobutyric acid) domains. Chemical Communications (Cambridge, England). 48: 3397-9. PMID 22363936 DOI: 10.1039/C2Cc00060A |
0.715 |
|
2012 |
Brown RA, Marcelli T, De Poli M, Solà J, Clayden J. Induction of unexpected left-handed helicity by an N-terminal L-amino acid in an otherwise achiral peptide chain. Angewandte Chemie (International Ed. in English). 51: 1395-9. PMID 22294355 DOI: 10.1002/Anie.201107583 |
0.544 |
|
2011 |
Fletcher SP, Solà J, Holt D, Brown RA, Clayden J. Synthesis of enantiomerically enriched (R)-C-labelled 2-aminoisobutyric acid (Aib) by conformational memory in the alkylation of a derivative of L-alanine. Beilstein Journal of Organic Chemistry. 7: 1304-9. PMID 22043239 DOI: 10.3762/Bjoc.7.152 |
0.644 |
|
2011 |
Solà J, Morris GA, Clayden J. Measuring screw-sense preference in a helical oligomer by comparison of 13C NMR signal separation at slow and fast exchange. Journal of the American Chemical Society. 133: 3712-5. PMID 21351795 DOI: 10.1021/Ja1097034 |
0.5 |
|
2011 |
Solà J, Helliwell M, Clayden J. Interruption of a 3(10)-helix by a single Gly residue in a poly-Aib motif: a crystallographic study. Biopolymers. 95: 62-9. PMID 20725951 DOI: 10.1002/Bip.21535 |
0.508 |
|
2010 |
Solà J, Fletcher SP, Castellanos A, Clayden J. Nanometer-range communication of stereochemical information by reversible switching of molecular helicity. Angewandte Chemie (International Ed. in English). 49: 6836-9. PMID 20687056 DOI: 10.1002/Anie.201001130 |
0.599 |
|
2010 |
Solà J, Helliwell M, Clayden J. N-versus C-terminal control over the screw-sense preference of the configurationally achiral, conformationally helical peptide motif Aib(8)GlyAib(8). Journal of the American Chemical Society. 132: 4548-9. PMID 20232805 DOI: 10.1021/Ja100662D |
0.565 |
|
2010 |
Brun S, Parera M, Pla-Quintana A, Roglans A, León T, Achard T, Solà J, Verdaguer X, Riera A. Chiral N-phosphino sulfinamide ligands in rhodium(I)-catalyzed [2+2+2] cycloaddition reactions Tetrahedron. 66: 9032-9040. DOI: 10.1016/J.Tet.2010.09.009 |
0.655 |
|
2010 |
Solà J, Riera A, Verdaguer X. Synthesis of a new camphor derived P,S(O) ligand. The importance of C–H⋯O bonding in the ligand exchange reactions with Co2(μ-alkyne)(CO)6 complexes Journal of Organometallic Chemistry. 695: 2377-2380. DOI: 10.1016/J.Jorganchem.2010.07.021 |
0.621 |
|
2009 |
Clayden J, Castellanos A, Solà J, Morris GA. Quantifying end-to-end conformational communication of chirality through an achiral peptide chain. Angewandte Chemie (International Ed. in English). 48: 5962-5. PMID 19569153 DOI: 10.1002/Anie.200901892 |
0.515 |
|
2008 |
Revés M, Achard T, Solà J, Riera A, Verdaguer X. N-phosphino-p-tolylsulfinamide ligands: Synthesis, stability, and application to the intermolecular Pauson-Khand reaction Journal of Organic Chemistry. 73: 7080-7087. PMID 18729408 DOI: 10.1021/Jo800710N |
0.624 |
|
2007 |
Solà J, Revés M, Riera A, Verdaguer X. N-phosphino sulfinamide ligands: An efficient manner to combine sulfur chirality and phosphorus coordination behavior Angewandte Chemie - International Edition. 46: 5020-5023. PMID 17523205 DOI: 10.1002/Anie.200701040 |
0.599 |
|
2007 |
Lledó A, Solà J, Verdaguer X, Riera A, Maestro MA. PuPHOS and CamPHOS ligands in the intermolecular catalytic pauson-khand reaction Advanced Synthesis and Catalysis. 349: 2121-2128. DOI: 10.1002/Adsc.200700145 |
0.639 |
|
2006 |
Solà J, Riera A, Verdaguer X, Maestro MA. C-H⋯O hydrogen bond-directed ligand exchange reaction: Diastereoselective synthesis of P,S-bridged (μ-alkyne)Co2(CO) 4 complexes Organometallics. 25: 5795-5799. DOI: 10.1021/Om060656M |
0.635 |
|
2006 |
Solà J, Riera A, Verdaguer X, Maestro MA. Phosphine−Substrate Recognition through the CH···O Hydrogen Bond: Application to the Asymmetric Pauson−Khand Reaction [J. Am.Chem. Soc.2005,127, 13629−13633]. Journal of the American Chemical Society. 128: 13312-13312. DOI: 10.1021/Ja066395P |
0.333 |
|
2005 |
Solà J, Riera A, Verdaguer X, Maestro MA. Phosphine-substrate recognition through the C-H...O hydrogen bond: application to the asymmetric Pauson-Khand reaction. Journal of the American Chemical Society. 127: 13629-33. PMID 16190728 DOI: 10.1021/Ja053653U |
0.619 |
|
2005 |
Solà J, Riera A, Verdaguer X, Maestro MA. Phosphine-substrate recognition through the C-H⋯O hydrogen bond: Application to the asymmetric Pauson-Khand reaction Journal of the American Chemical Society. 127: 13629-13633. DOI: 10.1021/ja053653u |
0.571 |
|
2004 |
Solà J, Riera A, Pericàs MA, Verdaguer X, Maestro MA. Stereoselectivity in the intermolecular Pauson-Khand reaction of electron-deficient terminal alkynes Tetrahedron Letters. 45: 5387-5390. DOI: 10.1016/J.Tetlet.2004.05.083 |
0.666 |
|
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