Year |
Citation |
Score |
2022 |
Jackson OD, Stankevich KS, Cook MJ. Highly diastereo- and branched-selective rearrangement of substituted -alloc--allyl ynamides. Chemical Communications (Cambridge, England). PMID 36196849 DOI: 10.1039/d2cc03399b |
0.429 |
|
2022 |
Stankevich KS, Cook MJ. A Highly Stereospecific Claisen-Sakurai Approach to Densely Functionalized Cyclopentenols. The Journal of Organic Chemistry. 87: 12250-12256. PMID 36067340 DOI: 10.1021/acs.joc.2c01397 |
0.431 |
|
2018 |
Rovis T, Oberg K, Cochran B, Cook M. The Catalytic Alkylative Desymmetrization of Anhydrides in a Formal Synthesis of Ionomycin Synthesis. 50: 4343-4350. DOI: 10.1055/S-0037-1610108 |
0.736 |
|
2017 |
Alexander JR, Cook MJ. Formation of Ketenimines via the Palladium-Catalyzed Decarboxylative π-Allylic Rearrangement of N-Alloc Ynamides. Organic Letters. PMID 29052418 DOI: 10.1021/Acs.Orglett.7B02780 |
0.447 |
|
2015 |
Baddeley KL, Cao Q, Muldoon MJ, Cook MJ. Palladium-catalyzed oxidative synthesis of highly functionalized ortholactones. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 7726-30. PMID 25821187 DOI: 10.1002/Chem.201500862 |
0.493 |
|
2015 |
Reid JP, McAdam CA, Johnston AJ, Grayson MN, Goodman JM, Cook MJ. Base-mediated cascade rearrangements of aryl-substituted diallyl ethers. The Journal of Organic Chemistry. 80: 1472-98. PMID 25514457 DOI: 10.1021/Jo502403N |
0.448 |
|
2015 |
McLaughlin MG, McAdam CA, Cook MJ. MIDA-vinylsilanes: selective cross-couplings and applications to the synthesis of functionalized stilbenes. Organic Letters. 17: 10-3. PMID 25513732 DOI: 10.1021/Ol503065A |
0.685 |
|
2015 |
McAdam CA, McLaughlin MG, Cook MJ. An alkyne hydrosilylation-Hiyama coupling approach to highly functionalised 1,3-dienes Organic Chemistry Frontiers. 2: 510-514. DOI: 10.1039/C5Qo00002E |
0.682 |
|
2015 |
McAdam CA, McLaughlin MG, Cook MJ. ChemInform Abstract: An Alkyne Hydrosilylation-Hiyama Coupling Approach to Highly Functionalized 1,3-Dienes. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201540079 |
0.636 |
|
2014 |
Chavhan SW, Cook MJ. Silicon-directed rhenium-catalyzed allylic carbaminations and oxidative fragmentations of γ-silyl allylic alcohols. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 4891-5. PMID 24677380 DOI: 10.1002/Chem.201400104 |
0.48 |
|
2014 |
McLaughlin MG, Cook MJ. Highly diastereoselective hydrosilylations of allylic alcohols. Chemical Communications (Cambridge, England). 50: 3501-4. PMID 24557001 DOI: 10.1039/C4Cc00138A |
0.637 |
|
2013 |
Johnston AJ, McLaughlin MG, Reid JP, Cook MJ. NaH mediated isomerisation-allylation reaction of 1,3-substituted propenols. Organic & Biomolecular Chemistry. 11: 7662-6. PMID 24108362 DOI: 10.1039/C3Ob41857J |
0.662 |
|
2013 |
Dornan LM, Cao Q, Flanagan JC, Crawford JJ, Cook MJ, Muldoon MJ. Copper/TEMPO catalysed synthesis of nitriles from aldehydes or alcohols using aqueous ammonia and with air as the oxidant. Chemical Communications (Cambridge, England). 49: 6030-2. PMID 23719631 DOI: 10.1039/C3Cc42231C |
0.428 |
|
2013 |
McAdam CA, McLaughlin MG, Johnston AJ, Chen J, Walter MW, Cook MJ. Platinum catalysed hydrosilylation of propargylic alcohols. Organic & Biomolecular Chemistry. 11: 4488-502. PMID 23715614 DOI: 10.1039/C3Ob40496J |
0.687 |
|
2013 |
Chen J, Cook MJ. Palladium catalyzed decarboxylative rearrangement of N-alloc indoles. Organic Letters. 15: 1088-91. PMID 23421978 DOI: 10.1021/ol400110c |
0.448 |
|
2012 |
McLaughlin MG, Cook MJ. Domino alkene-isomerization-Claisen rearrangement strategy to substituted allylsilanes. The Journal of Organic Chemistry. 77: 2058-63. PMID 22235747 DOI: 10.1021/Jo202560G |
0.705 |
|
2012 |
Flanagan JCA, Dornan LM, McLaughlin MG, McCreanor NG, Cook MJ, Muldoon MJ. The synthesis of N-heterocycles via copper/TEMPO catalysed aerobic oxidation of amino alcohols Green Chemistry. 14: 1281. DOI: 10.1039/C2Gc35062A |
0.662 |
|
2012 |
Flanagan JCA, Dornan LM, McLaughlin MG, McCreanor NG, Cook MJ, Muldoon MJ. ChemInform Abstract: The Synthesis of N-Heterocycles via Copper/TEMPO Catalyzed Aerobic Oxidation of Amino Alcohols. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201240132 |
0.633 |
|
2011 |
McLaughlin MG, Cook MJ. PtCl2/XPhos: a highly efficient and readily available catalyst for the hydrosilylation of propargylic alcohols. Chemical Communications (Cambridge, England). 47: 11104-6. PMID 21909537 DOI: 10.1039/C1Cc14433B |
0.672 |
|
2009 |
Cook MJ, Rovis T. Enantioselective rhodium-catalyzed alkylative desymmetrization of 3,5-dimethylglutaric anhydride Synthesis. 335-338. DOI: 10.1055/S-0028-1083275 |
0.671 |
|
2009 |
Johnson JB, Cook MJ, Rovis T. Ligand differentiated complementary Rh-catalyst systems for the enantioselective desymmetrization of meso-cyclic anhydrides Tetrahedron. 65: 3202-3210. DOI: 10.1016/J.Tet.2008.10.075 |
0.595 |
|
2007 |
Cook MJ, Rovis T. Rhodium-catalyzed enantioselective desymmetrization of meso-3,5-dimethyl glutaric anhydride: a general strategy to syn-deoxypolypropionate synthons. Journal of the American Chemical Society. 129: 9302-3. PMID 17622150 DOI: 10.1021/Ja073269S |
0.623 |
|
2005 |
Cook MJ, Fleming DW, Gallagher T. Microwave-assisted, regioselective, Petasis olefination of unsymmetrical oxalates. Formation of pyruvate-based enol ethers and enamines Tetrahedron Letters. 46: 297-300. DOI: 10.1016/J.Tetlet.2004.11.070 |
0.583 |
|
2005 |
Cook MJ, Fleming DW, Gallagher T. Microwave-Assisted, Regioselective, Petasis Olefination of Unsymmetrical Oxalates. Formation of Pyruvate-Based Enol Ethers and Enamines. Cheminform. 36. DOI: 10.1002/CHIN.200518047 |
0.595 |
|
2004 |
Cook MJ, Fletcher MJE, Gray D, Lovell PJ, Gallagher T. Highly stereoselective addition of organozinc reagents to pentopyranose derived glycals: Effect of protecting group and assignment of C-glycoside stereochemistry Tetrahedron. 60: 5085-5092. DOI: 10.1016/J.Tet.2004.04.004 |
0.542 |
|
2004 |
Cook MJ, Fletcher MJE, Gray D, Lovell PJ, Gallagher T. Highly Stereoselective Addition of Organozinc Reagents to Pentopyranose Derived Glycals: Effect of Protecting Group and Assignment of C-Glycoside Stereochemistry. Cheminform. 35. DOI: 10.1002/CHIN.200438204 |
0.561 |
|
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