Year |
Citation |
Score |
2019 |
Vemula SR, Chhoun MR, Cook GR. Well-Defined Pre-Catalysts in Amide and Ester Bond Activation. Molecules (Basel, Switzerland). 24. PMID 30634382 DOI: 10.3390/Molecules24020215 |
0.41 |
|
2018 |
Vemula SR, Kumar D, Cook GR. Bismuth-Catalyzed Synthesis of 2-Substituted Quinazolinones. Tetrahedron Letters. 59: 3801-3805. PMID 31274936 DOI: 10.1016/J.Tetlet.2018.09.014 |
0.534 |
|
2016 |
Kumar D, Vemula SR, Balasubramanian N, Cook GR. Indium-Mediated Stereoselective Allylation. Accounts of Chemical Research. PMID 27700084 DOI: 10.1021/Acs.Accounts.6B00362 |
0.696 |
|
2016 |
Vemula SR, Kumar D, Cook GR. Palladium-Catalyzed Allylic Amidation with N-Heterocycles via sp3 C–H Oxidation Acs Catalysis. 6: 5295-5301. DOI: 10.1021/Acscatal.6B01818 |
0.57 |
|
2016 |
Kumar D, Vemula SR, Cook GR. Recent Advances in the Catalytic Synthesis of α-Ketoamides Acs Catalysis. 6: 4920-4945. DOI: 10.1021/Acscatal.6B01116 |
0.451 |
|
2016 |
Kumar D, Vemula SR, Cook GR. Merging C–H Bond Functionalization with Amide Alcoholysis: En Route to 2-Aminopyridines Acs Catalysis. 6: 3531-3536. DOI: 10.1021/Acscatal.6B00728 |
0.498 |
|
2015 |
Balasubramanian N, Mandal T, Cook GR. Highly diastereoselective palladium-catalyzed indium-mediated allylation of chiral hydrazones. Organic Letters. 17: 314-7. PMID 25565466 DOI: 10.1021/Ol5034207 |
0.643 |
|
2015 |
Kumar D, Vemula SR, Cook GR. Highly chemo- and regioselective allylic substitution with tautomerizable heteroarenes Green Chemistry. 17: 4300-4306. DOI: 10.1039/C5Gc01028D |
0.487 |
|
2015 |
Vemula SR, Kumar D, Cook GR. N-Boc-glycine-assisted indium-mediated allylation reaction: A sustainable approach Tetrahedron Letters. 56: 3322-3325. DOI: 10.1016/J.Tetlet.2015.01.036 |
0.559 |
|
2015 |
Vemula SR, Kumar D, Cook GR. ChemInform Abstract: N-Boc-Glycine-Assisted Indium-Mediated Allylation Reaction: A Sustainable Approach. Cheminform. 46: no-no. DOI: 10.1002/chin.201540134 |
0.465 |
|
2011 |
Singh RK, Mandal T, Balasubramanian N, Cook G, Srivastava DK. Coumarin-suberoylanilide hydroxamic acid as a fluorescent probe for determining binding affinities and off-rates of histone deacetylase inhibitors. Analytical Biochemistry. 408: 309-15. PMID 20816742 DOI: 10.1016/J.Ab.2010.08.040 |
0.475 |
|
2010 |
TROST BM, COOK GR. ChemInform Abstract: An Asymmetric Synthesis (-)-Epibatidine. Cheminform. 28: no-no. DOI: 10.1002/chin.199705260 |
0.431 |
|
2010 |
COOK GR, BEHOLZ LG, STILLE JR. ChemInform Abstract: Construction of Hydroxylated Alkaloids (.+-.)-Mannonolactam, (.+-.)- Deoxymannojirimycin, and (.+-.)-Prosopinine Through Aza-Anellation. Cheminform. 25: no-no. DOI: 10.1002/chin.199451261 |
0.732 |
|
2010 |
COOK GR, STILLE JR. ChemInform Abstract: Preparation and 3-Aza-Cope Rearrangement of N-Alkyl-N-allyl Enamines. Cheminform. 23: no-no. DOI: 10.1002/chin.199206095 |
0.309 |
|
2009 |
Samanta D, Kargbo RB, Cook GR. Asymmetric synthesis of aminochromanes via intramolecular indium-mediated allylation of chiral hydrazones. The Journal of Organic Chemistry. 74: 7183-6. PMID 19702255 DOI: 10.1021/Jo901195G |
0.759 |
|
2008 |
Hayashi R, Cook GR. Bi(OTf)(3)-Catalyzed 5-Exo-Trig Cyclization via Halide Activation. Tetrahedron Letters. 49: 3888-3890. PMID 19122872 DOI: 10.1016/J.Tetlet.2008.04.067 |
0.605 |
|
2008 |
Hayashi R, Cook GR. ChemInform Abstract: Bi(OTf)3-Catalyzed 5-exo-Trig Cyclization via Halide Activation. Cheminform. 39. DOI: 10.1002/chin.200836056 |
0.325 |
|
2007 |
Hayashi R, Jin X, Cook GR. Synthesis and evaluation of novel heterocyclic MMP inhibitors. Bioorganic & Medicinal Chemistry Letters. 17: 6864-70. PMID 18029173 DOI: 10.1016/J.Bmcl.2007.10.020 |
0.488 |
|
2007 |
Kargbo R, Takahashi Y, Bhor S, Cook GR, Lloyd-Jones GC, Shepperson IR. Readily accessible, modular, and tuneable BINOL 3,3'-perfluoroalkylsulfones: highly efficient catalysts for enantioselective in-mediated imine allylation. Journal of the American Chemical Society. 129: 3846-7. PMID 17352482 DOI: 10.1021/Ja070742T |
0.687 |
|
2007 |
Hayashi R, Cook GR. Remarkably mild and efficient intramolecular Friedel-Crafts cyclization catalyzed by In(III). Organic Letters. 9: 1311-4. PMID 17346056 DOI: 10.1021/Ol070235G |
0.6 |
|
2007 |
Kargbo RB, Cook GR. Stereoselective indium-mediated allylation reactions Current Organic Chemistry. 11: 1287-1309. DOI: 10.2174/138527207782023139 |
0.587 |
|
2007 |
Kaneko M, Hayashi R, Cook GR. Intermolecular Friedel-Crafts reaction catalyzed by InCl3 Tetrahedron Letters. 48: 7085-7087. DOI: 10.1016/J.Tetlet.2007.08.011 |
0.615 |
|
2006 |
Cook GR, Hayashi R. Atom transfer cyclization catalyzed by InCl3 via halogen activation. Organic Letters. 8: 1045-8. PMID 16524264 DOI: 10.1021/Ol052802A |
0.546 |
|
2006 |
Cook GR, Xu W. Tandem palladium-catalyzed allene arylation and oxazoline formation Heterocycles. 67: 215-232. DOI: 10.3987/Com-05-S(T)16 |
0.475 |
|
2006 |
Cook GR. Synthesis of Amides from Amines Cheminform. 37. DOI: 10.1002/chin.200605270 |
0.318 |
|
2005 |
Cook GR, Kargbo R, Maity B. Catalytic enantioselective indium-mediated allylation of hydrazones. Organic Letters. 7: 2767-70. PMID 15957942 DOI: 10.1021/Ol051160O |
0.61 |
|
2005 |
Cook GR, Saraswathiamma M. Hydrogen-bond directed palladium-catalyzed allylic substitution of cyclic substrates Tetrahedron Letters. 46: 6491-6494. DOI: 10.1016/J.Tetlet.2005.07.096 |
0.37 |
|
2004 |
Cook GR, Sun L. Nitrogen heterocycles via palladium-catalyzed carbocyclization. Formal synthesis of (+)-alpha-allokainic acid. Organic Letters. 6: 2481-4. PMID 15228309 DOI: 10.1002/CHIN.200445202 |
0.301 |
|
2004 |
Cook GR, Maity BC, Kargbo R. Highly diastereoselective indium-mediated allylation of chiral hydrazones. Organic Letters. 6: 1741-3. PMID 15151403 DOI: 10.1021/Ol0496172 |
0.657 |
|
2003 |
Cook GR, Yu H, Sankaranarayanan S, Shanker PS. Hydrogen bond directed highly regioselective palladium-catalyzed allylic substitution. Journal of the American Chemical Society. 125: 5115-20. PMID 12708863 DOI: 10.1021/Ja028426W |
0.394 |
|
2002 |
Cook GR, Pararajasingham K. Stereoselective synthesis of D-erythro- and L-threo-sphinganines via palladium-catalyzed equilibration and Suzuki coupling Tetrahedron Letters. 43: 9027-9029. DOI: 10.1016/S0040-4039(02)02309-2 |
0.343 |
|
2001 |
Cook GR, Sankaranarayanan S. Palladium-mediated regiodivergent kinetic resolution. Organic Letters. 3: 3531-3. PMID 11678700 DOI: 10.1021/Ol016633F |
0.414 |
|
1999 |
Cook GR, Shanker PS, Peterson SL. Asymmetric synthesis of the balanol heterocycle via a palladium-mediated epimerization and olefin metathesis. Organic Letters. 1: 615-7. PMID 10823189 DOI: 10.1021/Ol990705+ |
0.425 |
|
1999 |
Sibi MP, Chen JX, Cook GR. Reversal of stereochemistry in diethylzinc addition to aldehydes by a simple change of the backbone substituent in L-serine derived ligands Tetrahedron Letters. 40: 3301-3304. DOI: 10.1016/S0040-4039(99)00480-3 |
0.34 |
|
1999 |
Sibi MP, Cook GR, Liu P. Enantioselective reduction of ketones. Examination of bifunctional ligands Tetrahedron Letters. 40: 2477-2480. DOI: 10.1016/S0040-4039(99)00281-6 |
0.365 |
|
1999 |
Cook GR, Shanker PS, Pararajasingham K. Palladium-mediated dynamic kinetic resolution: Stereoselective synthesis of vicinal diamines Angewandte Chemie - International Edition. 38: 110-113. DOI: 10.1002/(Sici)1521-3773(19990115)38:1/2<110::Aid-Anie110>3.0.Co;2-L |
0.458 |
|
1998 |
Cook GR, Shanker PS. Chloride effect on the palladium-catalyzed allylic substitution vs elimination of cyclic vinyloxazolidinones and oxazolines Tetrahedron Letters. 39: 4991-4994. DOI: 10.1016/S0040-4039(98)00976-9 |
0.414 |
|
1998 |
Cook GR, Shanker PS. Palladium-catalyzed formation and stereoselecttve isomerization of 5-vinyloxazolines. Application to the formal synthesis of (S,S)-4-amino-3-hydroxy-5-phenylpentanoic acid Tetrahedron Letters. 39: 3405-3408. DOI: 10.1016/S0040-4039(98)00534-6 |
0.427 |
|
1996 |
Trost BM, Cook GR. An asymmetric synthesis (-)-epibatidine Tetrahedron Letters. 37: 7485-7488. DOI: 10.1016/0040-4039(96)01739-X |
0.456 |
|
1994 |
Cook GR, Beholz LG, Stille JR. Construction of Hydroxylated Alkaloids (.+-.)-Mannonolactam, (.+-.)-Deoxymannojirimycin, and (.+-.)-Prosopinine through Aza-Annulation The Journal of Organic Chemistry. 59: 3575-3584. DOI: 10.1021/Jo00092A015 |
0.77 |
|
1994 |
Cook GR, Beholz LG, Stille JR. Aza-annulation as a route to hydroxylated alkaloid lipids. The synthesis of (±)-prosopinine Tetrahedron Letters. 35: 1669-1672. DOI: 10.1016/0040-4039(94)88315-7 |
0.756 |
|
1994 |
Cook GR, Beholz LG, Stille JR. Construction of hydroxylated alkaloids (±)-mannonolactam, (±)-deoxymannojirimycin, and (±)-prosopinine through aza-annulation Journal of Organic Chemistry. 59: 3575-3584. |
0.718 |
|
1992 |
Barta NS, Cook GR, Landis MS, Stille JR. Studies of the regiospecific 3-aza-cope rearrangement promoted by electrophilic reagents Journal of Organic Chemistry. 57: 7188-7194. DOI: 10.1021/Jo00052A037 |
0.752 |
|
1992 |
Cook GR, Barta NS, Stille JR. Lewis acid-promoted 3-aza-Cope rearrangement of N-alkyl-N-allylenamines Journal of Organic Chemistry. 57: 461-467. |
0.744 |
|
1991 |
Cook GR, Stille JR. Preparation of 3-aza-Cope rearrangement of N-alkyl-N-allyl enamines Journal of Organic Chemistry. 56: 5578-5583. DOI: 10.1021/Jo00019A021 |
0.692 |
|
1991 |
Cook GR, Stille JR. Preparation and 3-aza-cope rearrangement of N-alkyl-N-allyl enamines Journal of Organic Chemistry. 56: 5578-5583. |
0.673 |
|
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