Year |
Citation |
Score |
2020 |
Montalvo-Acosta JJ, Dryzhakov M, Richmond E, Cecchini M, Moran J. A Supramolecular Model for the Co-Catalytic Role of Nitro Compounds in Brønsted Acid Catalyzed Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32365243 DOI: 10.1002/Chem.202000368 |
0.674 |
|
2019 |
Noel F, Vukovic VD, Yi J, Richmond E, Kravljanac P, Moran J. Catalytic Synthesis of Trifluoromethylated Allenes, Indenes, Chromenes and Olefins from Propargylic Alcohols in HFIP. The Journal of Organic Chemistry. PMID 31741385 DOI: 10.1021/Acs.Joc.9B02398 |
0.738 |
|
2018 |
Richmond E, Yi J, Vuković VD, Sajadi F, Rowley CN, Moran J. Ring-opening hydroarylation of monosubstituted cyclopropanes enabled by hexafluoroisopropanol. Chemical Science. 9: 6411-6416. PMID 30310570 DOI: 10.1039/C8Sc02126K |
0.709 |
|
2018 |
Richmond E, Vuković VD, Moran J. Nucleophilic Ring Opening of Donor-Acceptor Cyclopropanes Catalyzed by a Brønsted Acid in Hexafluoroisopropanol. Organic Letters. PMID 29345947 DOI: 10.1021/Acs.Orglett.7B03688 |
0.741 |
|
2017 |
Vuković VD, Richmond E, Wolf E, Moran J. Catalytic Friedel-Crafts Reactions of Highly Electronically Deactivated Benzylic Alcohols. Angewandte Chemie (International Ed. in English). PMID 28156038 DOI: 10.1002/Anie.201612573 |
0.739 |
|
2017 |
Richmond E, Moran J. Recent Advances in Nickel Catalysis Enabled by Stoichiometric Metallic Reducing Agents Synthesis. 50: 499-513. DOI: 10.1055/S-0036-1591853 |
0.589 |
|
2017 |
Dryzhakov M, Richmond E, Li G, Moran J. Catalytic B(C6F5)3H2O-promoted defluorinative functionalization of tertiary aliphatic fluorides Journal of Fluorine Chemistry. 193: 45-51. DOI: 10.1016/J.Jfluchem.2016.11.005 |
0.623 |
|
2016 |
Richmond E, Khan IU, Moran J. Enantioselective and Regiodivergent Functionalization of N-Allylcarbamates by Mechanistically Divergent Multicatalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27461524 DOI: 10.1002/Chem.201602792 |
0.648 |
|
2016 |
Moran J, Richmond E. Harnessing Complex Mixtures for Catalyst Discovery Synlett. 27: 2637-2643. DOI: 10.1055/S-0036-1588334 |
0.62 |
|
2015 |
Wolf E, Richmond E, Moran J. Identifying lead hits in catalyst discovery by screening and deconvoluting complex mixtures of catalyst components. Chemical Science. 6: 2501-2505. PMID 29308159 DOI: 10.1039/C5Sc00268K |
0.653 |
|
2015 |
Richmond E, Moran J. Ligand Control of E/Z Selectivity in Nickel-Catalyzed Transfer Hydrogenative Alkyne Semireduction. The Journal of Organic Chemistry. 80: 6922-9. PMID 26030191 DOI: 10.1021/Acs.Joc.5B01047 |
0.635 |
|
2015 |
Richmond E, Ling KB, Duguet N, Manton LB, Çelebi-Ölçüm N, Lam YH, Alsancak S, Slawin AM, Houk KN, Smith AD. An asymmetric pericyclic cascade approach to 3-alkyl-3-aryloxindoles: generality, applications and mechanistic investigations. Organic & Biomolecular Chemistry. 13: 1807-17. PMID 25501712 DOI: 10.1039/C4Ob02526A |
0.384 |
|
2015 |
Dryzhakov M, Richmond E, Moran J. Recent Advances in Direct Catalytic Dehydrative Substitution of Alcohols Synthesis (Germany). DOI: 10.1055/S-0035-1560396 |
0.679 |
|
2015 |
Wolf E, Richmond E, Moran J. Identifying lead hits in catalyst discovery by screening and deconvoluting complex mixtures of catalyst components Chemical Science. 6: 2501-2505. DOI: 10.1039/c5sc00268k |
0.563 |
|
2012 |
Richmond E, Duguet N, Slawin AM, Lébl T, Smith AD. Asymmetric pericyclic cascade approach to spirocyclic oxindoles. Organic Letters. 14: 2762-5. PMID 22583112 DOI: 10.1021/Ol300982F |
0.408 |
|
2011 |
Çelebi-Ölçüm N, Lam YH, Richmond E, Ling KB, Smith AD, Houk KN. Pericyclic cascade with chirality transfer: reaction pathway and origin of enantioselectivity of the hetero-Claisen approach to oxindoles. Angewandte Chemie (International Ed. in English). 50: 11478-82. PMID 21976415 DOI: 10.1002/Anie.201105412 |
0.43 |
|
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