Year |
Citation |
Score |
2018 |
Fieser ME, Schimler SD, Mitchell LA, Wilborn EG, John A, Hogan LT, Benson B, LaPointe AM, Tolman WB. Dual-catalytic decarbonylation of fatty acid methyl esters to form olefins. Chemical Communications (Cambridge, England). PMID 29938264 DOI: 10.1039/C8Cc03823F |
0.558 |
|
2017 |
John A, Bolte M, Lerner HW, Wagner M. A Vicinal Electrophilic Diborylation Reaction Furnishes Doubly Boron-Doped Polycyclic Aromatic Hydrocarbons. Angewandte Chemie (International Ed. in English). PMID 28402016 DOI: 10.1002/Anie.201701591 |
0.316 |
|
2017 |
John A, Dereli B, Ortuño MA, Johnson HE, Hillmyer MA, Cramer CJ, Tolman WB. Selective Decarbonylation of Fatty Acid Esters to Linear α-Olefins Organometallics. 36: 2956-2964. DOI: 10.1021/Acs.Organomet.7B00411 |
0.627 |
|
2017 |
John A, Hillmyer MA, Tolman WB. Anhydride-Additive-Free Nickel-Catalyzed Deoxygenation of Carboxylic Acids to Olefins Organometallics. 36: 506-509. DOI: 10.1021/Acs.Organomet.6B00940 |
0.659 |
|
2016 |
John A, Miranda MO, Ding K, Dereli B, Ortuno MA, Lapointe AM, Coates GW, Cramer CJ, Tolman WB. Nickel Catalysts for the Dehydrative Decarbonylation of Carboxylic Acids to Alkenes Organometallics. 35: 2391-2400. DOI: 10.1021/Acs.Organomet.6B00415 |
0.668 |
|
2015 |
Ding K, John A, Shin J, Lee Y, Quinn T, Tolman WB, Hillmyer MA. High-Performance Pressure-Sensitive Adhesives from Renewable Triblock Copolymers. Biomacromolecules. 16: 2537-9. PMID 26214728 DOI: 10.1021/Acs.Biomac.5B00754 |
0.511 |
|
2015 |
John A, Hogan LT, Hillmyer MA, Tolman WB. Olefins from biomass feedstocks: catalytic ester decarbonylation and tandem Heck-type coupling. Chemical Communications (Cambridge, England). 51: 2731-3. PMID 25579879 DOI: 10.1039/C4Cc09003A |
0.652 |
|
2013 |
John A, Byun J, Nicholas KM. Copper-catalyzed C(sp2)-H amidation of unactivated arenes by N-tosyloxycarbamates. Chemical Communications (Cambridge, England). 49: 10965-7. PMID 24132225 DOI: 10.1039/C3Cc46412A |
0.602 |
|
2013 |
John A, Modak S, Madasu M, Katari M, Ghosh P. Palladium complexes of the N-fused heterocycle derived abnormal N-heterocyclic carbenes for the much-preferred Cu-free and the amine-free Sonogashira coupling in air Polyhedron. 64: 20-29. DOI: 10.1016/J.Poly.2013.01.062 |
0.665 |
|
2012 |
John A, Nicholas KM. Palladium catalyzed C-H functionalization of O-arylcarbamates: selective ortho-bromination using NBS. The Journal of Organic Chemistry. 77: 5600-5. PMID 22663545 DOI: 10.1021/Jo300713H |
0.629 |
|
2012 |
John A, Nicholas KM. Copper-Mediated Multiple C–H Functionalization of AromaticN-Heterocycles: Bromoamination of Indoles and Pyrroles Organometallics. 31: 7914-7920. DOI: 10.1021/Om300553B |
0.588 |
|
2011 |
John A, Nicholas KM. Copper-catalyzed amidation of 2-phenylpyridine with oxygen as the terminal oxidant. The Journal of Organic Chemistry. 76: 4158-62. PMID 21401207 DOI: 10.1021/Jo200409H |
0.593 |
|
2010 |
John A, Shaikh MM, Butcher RJ, Ghosh P. Highly efficient palladium precatalysts of homoscorpionate bispyrazolyl ligands for the more challenging Suzuki-Miyaura cross-coupling of aryl chlorides. Dalton Transactions (Cambridge, England : 2003). 39: 7353-63. PMID 20607167 DOI: 10.1039/C003174G |
0.621 |
|
2010 |
John A, Ghosh P. Fascinating frontiers of N/O-functionalized N-heterocyclic carbene chemistry: from chemical catalysis to biomedical applications. Dalton Transactions (Cambridge, England : 2003). 39: 7183-206. PMID 20495733 DOI: 10.1039/C002475A |
0.615 |
|
2010 |
John A, Shaikh MM, Ghosh P. Suzuki–Miyaura cross-coupling of aryl chlorides catalyzed by palladium precatalysts of N/O-functionalized pyrazolyl ligands Inorganica Chimica Acta. 363: 3113-3121. DOI: 10.1016/J.Ica.2010.04.006 |
0.666 |
|
2009 |
John A, Shaikh MM, Ghosh P. Palladium complexes of abnormal N-heterocyclic carbenes as precatalysts for the much preferred Cu-free and amine-free Sonogashira coupling in air in a mixed-aqueous medium. Dalton Transactions (Cambridge, England : 2003). 10581-91. PMID 20023883 DOI: 10.1039/B913068C |
0.664 |
|
2008 |
Panda MK, John A, Shaikh MM, Ghosh P. Mimicking the intradiol catechol cleavage activity of catechol dioxygenase by high-spin iron(III) complexes of a new class of a facially bound [N2O] ligand. Inorganic Chemistry. 47: 11847-56. PMID 19006298 DOI: 10.1021/Ic801576F |
0.698 |
|
2008 |
John A, Shaikh MM, Ghosh P. Structural and functional mimic of galactose oxidase by a copper complex of a sterically demanding [N2O2] ligand. Dalton Transactions (Cambridge, England : 2003). 2815-24. PMID 18478142 DOI: 10.1039/B801496E |
0.62 |
|
2007 |
John A, Katiyar V, Pang K, Shaikh MM, Nanavati H, Ghosh P. Ni(II) and Cu(II) complexes of phenoxy-ketimine ligands: Synthesis, structures and their utility in bulk ring-opening polymerization (ROP) of l-lactide Polyhedron. 26: 4033-4044. DOI: 10.1016/J.Poly.2007.04.039 |
0.627 |
|
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