| Year |
Citation |
Score |
| 2015 |
Goren K, Karabline-Kuks J, Shiloni Y, Barak-Kulbak E, Miller SJ, Portnoy M. Multivalency as a key factor for high activity of selective supported organocatalysts for the Baylis-Hillman reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 1191-7. PMID 25376519 DOI: 10.1002/Chem.201404560 |
0.364 |
|
| 2010 |
Goren K, Portnoy M. Supported N-alkylimidazole-decorated dendrons as heterogeneous catalysts for the Baylis-Hillman reaction. Chemical Communications (Cambridge, England). 46: 1965-7. PMID 20198268 DOI: 10.1039/b915577e |
0.37 |
|
| 2008 |
Mansour A, Kehat T, Portnoy M. Dendritic effects in catalysis by Pd complexes of bidentate phosphines on a dendronized support: Heck vs. carbonylation reactions. Organic & Biomolecular Chemistry. 6: 3382-7. PMID 18802646 DOI: 10.1039/b809715a |
0.57 |
|
| 2007 |
Kehat T, Portnoy M. Polymer-supported proline-decorated dendrons: dendritic effect in asymmetric aldol reaction. Chemical Communications (Cambridge, England). 2823-5. PMID 17609788 DOI: 10.1039/b703016a |
0.367 |
|
| 2007 |
Dahan A, Portnoy M. Pd catalysis on dendronized solid support: generation effects and the influence of the backbone structure. Journal of the American Chemical Society. 129: 5860-9. PMID 17439211 DOI: 10.1021/ja065265d |
0.435 |
|
| 2005 |
Weissberg A, Halak B, Portnoy M. The first solid-phase synthesis of bis(oxazolinyl)pyridine ligands. The Journal of Organic Chemistry. 70: 4556-9. PMID 15903347 DOI: 10.1021/jo050237j |
0.334 |
|
| 2003 |
Dahan A, Portnoy M. Remarkable dendritic effect in the polymer-supported catalysis of the Heck arylation of olefins. Organic Letters. 5: 1197-200. PMID 12688718 DOI: 10.1021/ol0340181 |
0.446 |
|
| 2002 |
Dahan A, Portnoy M. Dendritic effect in polymer-supported catalysis of the intramolecular Pauson-Khand reaction. Chemical Communications (Cambridge, England). 2700-1. PMID 12510306 DOI: 10.1039/b207625j |
0.399 |
|
| 1994 |
Portnoy M, Ben-David Y, Rousso I, Milstein D. Reactions of electron-rich arylpalladium complexes with olefins. Origin of the chelate effect in vinylation catalysis Organometallics. 13: 3465-3479. DOI: 10.1021/Om00021A021 |
0.623 |
|
| 1994 |
Portnoy M, Milstein D. A binuclear palladium(I) hydride. Formation, reactions, and catalysis Organometallics. 13: 600-609. DOI: 10.1021/Om00014A035 |
0.59 |
|
| 1993 |
Portnoy M, Ben-David Y, Milstein D. Clarification of a remarkable chelate effect leads to palladium-catalyzed base-free olefin arylation Organometallics. 12: 4734-4735. DOI: 10.1021/Om00036A008 |
0.618 |
|
| 1993 |
Portnoy M, Milstein D. Mechanism of aryl chloride oxidative addition to chelated palladium(0) complexes Organometallics. 12: 1665-1673. DOI: 10.1021/Om00029A026 |
0.594 |
|
| 1993 |
Portnoy M, Milstein D. Chelate effect on the structure and reactivity of electron-rich palladium complexes and its relevance to catalysis Organometallics. 12: 1655-1664. DOI: 10.1021/Om00029A025 |
0.564 |
|
| 1992 |
Ben-David Y, Portnoy M, Gozin M, Milstein D. Palladium-catalyzed vinylation of aryl chlorides. Chelate effect in catalysis Organometallics. 11: 1995-1996. DOI: 10.1021/Om00042A008 |
0.675 |
|
| 1992 |
Ben-David Y, Gozin M, Portnoy M, Milstein D. Reductive dechlorination of aryl chlorides catalyzed by palladium complexes containing basic, chelating phosphines Journal of Molecular Catalysis. 73: 173-180. DOI: 10.1016/0304-5102(92)80070-W |
0.677 |
|
| 1991 |
Portnoy M, Frolow F, Milstein D. Methanol reduces an organopalladium(II) complex to a palladium(I) hydride. Crystallographic characterization of a hydrido-bridged palladium complex Organometallics. 10: 3960-3962. DOI: 10.1021/Om00058A007 |
0.59 |
|
| 1989 |
Ben-David Y, Portnoy M, Milstein D. Formylation of aryl chlorides catalysed by a palladium complex Journal of the Chemical Society, Chemical Communications. 1816-1817. DOI: 10.1039/C39890001816 |
0.695 |
|
| 1989 |
Ben-David Y, Portnoy M, Milstein D. Chelate-assisted, Pd-catalyzed efficient carbonylation of aryl chlorides Journal of the American Chemical Society. 111: 8742-8744. DOI: 10.1021/Ja00205A039 |
0.613 |
|
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