Year |
Citation |
Score |
2008 |
Goyal P, Zheng X, Weck M. Enhanced cooperativity in hydrolytic kinetic resolution of epoxides using poly(styrene) resin-supported dendronized co-(salen) catalysts Advanced Synthesis and Catalysis. 350: 1816-1822. DOI: 10.1002/Adsc.200800175 |
0.576 |
|
2008 |
Zheng X, Jones CW, Weck M. Engineering polymer-enhanced bimetallic cooperative interactions in the hydrolytic kinetic resolution of epoxides Advanced Synthesis and Catalysis. 350: 255-261. DOI: 10.1002/Adsc.200700339 |
0.579 |
|
2007 |
Minatti A, Zheng X, Buchwald SL. Synthesis of chiral 3-substituted indanones via an enantioselective reductive-Heck reaction. The Journal of Organic Chemistry. 72: 9253-8. PMID 17967034 DOI: 10.1021/Jo701741Y |
0.332 |
|
2007 |
Jain S, Zheng X, Jones CW, Weck M, Davis RJ. Importance of counterion reactivity on the deactivation of Co-salen catalysts in the hydrolytic kinetic resolution of epichlorohydrin. Inorganic Chemistry. 46: 8887-96. PMID 17850142 DOI: 10.1021/Ic700782F |
0.566 |
|
2007 |
Zheng X, Jones CW, Weck M. Ring-expanding olefin metathesis: a route to highly active unsymmetrical macrocyclic oligomeric co-salen catalysts for the hydrolytic kinetic resolution of epoxides. Journal of the American Chemical Society. 129: 1105-12. PMID 17263391 DOI: 10.1021/Ja0641406 |
0.599 |
|
2006 |
Holbach M, Zheng X, Burd C, Jones CW, Weck M. A practical one-pot synthesis of enantiopure unsymmetrical salen ligands. The Journal of Organic Chemistry. 71: 2903-6. PMID 16555853 DOI: 10.1021/Jo052614Y |
0.417 |
|
2005 |
Zheng X, Jones CW, Weck M. Poly(styrene)-supported co-salen complexes as efficient recyclable catalysts for the hydrolytic kinetic resolution of epichlorohydrin. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 576-83. PMID 16193524 DOI: 10.1002/Chem.200500786 |
0.6 |
|
2005 |
Sommer WJ, Yu K, Sears JS, Ji Y, Zheng X, Davis RJ, Sherrill CD, Jones CW, Week M. Investigations into the stability of tethered palladium(II) pincer complexes during heck catalysis Organometallics. 24: 4351-4361. DOI: 10.1021/Om048992V |
0.46 |
|
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