| Year |
Citation |
Score |
| 2020 |
Doyle MP, Marichev KO, Wang K, Greco N, Chen J, Lei J, Dong K. Strain-Induced Nucleophilic Ring Opening of Donor-Acceptor Cyclopropenes for Synthesis of Monosubstituted Succinic Acid Derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32853426 DOI: 10.1002/Chem.202003427 |
0.653 |
|
| 2020 |
Marichev KO, Dong K, Jensen J, Doyle MP, Wang R. Chiral 3-Acylglutaric Acid Derivatives from Strain-Induced Nucleophilic retro-Claisen Ring-Opening Reactions. The Journal of Organic Chemistry. PMID 32674577 DOI: 10.1021/Acs.Joc.0C01176 |
0.618 |
|
| 2019 |
Marichev KO, Dong K, Massey LA, Deng Y, De Angelis L, Wang K, Arman H, Doyle MP. Chiral donor-acceptor azetines as powerful reactants for synthesis of amino acid derivatives. Nature Communications. 10: 5328. PMID 31757976 DOI: 10.1038/S41467-019-13326-8 |
0.708 |
|
| 2019 |
Doyle MP, Marichev KO, Wang K, Dong K, Greco N, Massey L, Deng YM, Arman H. Synthesis of Chiral Tetrasubstituted Azetidines from Donor-Acceptor Azetines via Asymmetric Copper(I)-Catalyzed Imido-Ylide [3+1]-Cycloaddition with Metallo-Enolcarbenes. Angewandte Chemie (International Ed. in English). PMID 31496021 DOI: 10.1002/Anie.201909929 |
0.698 |
|
| 2019 |
Marichev KO, Doyle MP. Catalytic asymmetric cycloaddition reactions of enoldiazo compounds. Organic & Biomolecular Chemistry. PMID 30924829 DOI: 10.1039/C9Ob00478E |
0.638 |
|
| 2019 |
Dong K, Marichev KO, Xu X, Doyle MP. High Stereocontrol in the Preparation of Silyl-Protected γ-Substituted Enoldiazoacetates Synlett. 30: 1457-1461. DOI: 10.1055/S-0037-1611865 |
0.613 |
|
| 2019 |
Dong K, Marichev KO, Doyle MP. Role of Donor–Acceptor Cyclopropenes in Metal Carbene Reactions. Conversion of E-Substituted Enoldiazoacetates to Z-Substituted Metallo-Enolcarbenes Organometallics. 38: 4043-4050. DOI: 10.1021/Acs.Organomet.9B00427 |
0.573 |
|
| 2018 |
Adly FG, Marichev KO, Jensen JA, Arman H, Doyle MP. Enoldiazosulfones for Highly Enantioselective [3 + 3]-Cycloaddition with Nitrones Catalyzed by Copper(I) with Chiral BOX Ligands. Organic Letters. PMID 30550288 DOI: 10.1021/Acs.Orglett.8B03421 |
0.665 |
|
| 2018 |
Marichev KO, Wang Y, Carranco AM, Garcia EC, Yu ZX, Doyle MP. Rhodium(ii)-catalysed generation of cycloprop-1-en-1-yl ketones and their rearrangement to 5-aryl-2-siloxyfurans. Chemical Communications (Cambridge, England). PMID 30091758 DOI: 10.1039/C8Cc05623D |
0.625 |
|
| 2018 |
Marichev KO, Adly FG, Carranco AM, Garcia EC, Arman H, Doyle MP. Catalyst Choice for Highly Enantioselective [3 + 3]-Cycloaddition of Enoldiazocarbonyl Compounds Acs Catalysis. 8: 10392-10400. DOI: 10.1021/Acscatal.8B03391 |
0.692 |
|
| 2018 |
Marichev KO, Patil SA, Bugarin A. Recent advances in the synthesis, structural diversity, and applications of mesoionic 1,2,3-triazol-5-ylidene metal complexes Tetrahedron. 74: 2523-2546. DOI: 10.1016/J.Tet.2018.04.013 |
0.356 |
|
| 2017 |
Marichev KO, Garcia EC, Bhowmick KC, Wherritt DJ, Arman H, Doyle MP. Highly selective acylation of polyamines and aminoglycosides by 5-acyl-5-phenyl-1,5-dihydro-4H-pyrazol-4-ones. Chemical Science. 8: 7152-7159. PMID 29081946 DOI: 10.1039/C7Sc03184J |
0.528 |
|
| 2017 |
Marichev KO, Ramey JT, Arman H, Doyle MP. Highly Regio-, Diastereo-, and Enantioselective Rhodium-Catalyzed Intramolecular Cyclopropanation of (Z)-1,3-Dienyl Aryldiazoacetates. Organic Letters. PMID 28248515 DOI: 10.1021/Acs.Orglett.7B00119 |
0.665 |
|
| 2016 |
Marichev KO, Takacs JM. Ruthenium-Catalyzed Amination of Secondary Alcohols using Borrowing Hydrogen Methodology. Acs Catalysis. 6: 2205-2210. PMID 28936364 DOI: 10.1021/Acscatal.6B00175 |
0.447 |
|
| 2016 |
Qiu H, Deng Y, Marichev KO, Doyle MP. Diverse Pathways in Catalytic Reactions of Propargyl Aryldiazoacetates. Selectivity Between Three Reaction Sites. The Journal of Organic Chemistry. PMID 28029046 DOI: 10.1021/Acs.Joc.6B02770 |
0.713 |
|
| 2016 |
Marichev KO, Qiu H, Offield AC, Arman H, Doyle MP. Catalyst-free Rearrangement of Allenyl Aryldiazoacetates into 1,5-Dihydro-4H-pyrazol-4-ones. The Journal of Organic Chemistry. PMID 27607059 DOI: 10.1021/Acs.Joc.6B01833 |
0.708 |
|
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