| Year |
Citation |
Score |
| 2023 |
Warnica JM, Gleason JL. Mimicking enzymatic cation-π interactions in hydrazide catalyst design: access to -decalin frameworks. Chemical Communications (Cambridge, England). 59: 10496-10499. PMID 37559565 DOI: 10.1039/d3cc03351a |
0.306 |
|
| 2023 |
Barrett RRG, Campbell DA, Gleason JL. An Organocatalytic Oxy-Cope/Michael Cascade Reaction. Organic Letters. PMID 36701675 DOI: 10.1021/acs.orglett.2c04269 |
0.338 |
|
| 2022 |
Plamondon SJ, Gleason JL. Total Synthesis of (-)-3-Oxoisotaxodione. Organic Letters. 24: 2305-2309. PMID 35311261 DOI: 10.1021/acs.orglett.2c00444 |
0.416 |
|
| 2020 |
Sanders JN, Jun H, Yu RA, Gleason JL, Houk KN. Mechanism of an Organocatalytic Cope Rearrangement Involving Iminium Intermediates: Elucidating the Role of Catalyst Ring Size. Journal of the American Chemical Society. PMID 32865415 DOI: 10.1021/Jacs.0C08427 |
0.335 |
|
| 2019 |
Elmehriki AAH, Gleason JL. A Spiroalkylation Method for the Stereoselective Construction of α-Quaternary Carbons and Its Application to the Total Synthesis of ()-Puraquinonic Acid. Organic Letters. 21: 9729-9733. PMID 31756114 DOI: 10.1021/Acs.Orglett.9B03887 |
0.519 |
|
| 2019 |
Gleason JL, Plamondon SJ, Warnica JM, Kaldre D. Hydrazide-Catalyzed Polyene Cyclization: Asymmetric Organocatalytic Synthesis of cis-Decalins. Angewandte Chemie (International Ed. in English). PMID 31671228 DOI: 10.1002/Anie.201911952 |
0.477 |
|
| 2019 |
Hughes JME, Scarlata DA, Chen AC, Burch JD, Gleason JL. Aminoalkylation of [1.1.1]Propellane Enables Direct Access to High-Value 3-Alkylbicyclo[1.1.1]pentan-1-amines. Organic Letters. PMID 31407916 DOI: 10.1021/Acs.Orglett.9B02426 |
0.466 |
|
| 2018 |
Häggman NO, Zank B, Jun H, Kaldre D, Gleason JL. Diazepane Carboxylates as Organocatalysts in the Diels–Alder Reaction of α‐Substituted Enals European Journal of Organic Chemistry. 2018: 5412-5416. DOI: 10.1002/Ejoc.201801009 |
0.372 |
|
| 2017 |
Gleason JL, Hughes JME. A Concise, Enantioselective Total Synthesis of (-)-Virosaine A. Angewandte Chemie (International Ed. in English). PMID 28696549 DOI: 10.1002/Anie.201706273 |
0.504 |
|
| 2017 |
Hughes JME, Gleason JL. A bio-inspired cascade and a late-stage directed sp3 CH lithiation enables a concise total synthesis of (−)-virosaine A Tetrahedron. 74: 759-768. DOI: 10.1016/J.Tet.2017.12.026 |
0.488 |
|
| 2017 |
Larnaud F, Sulpizi A, Häggman NO, Hughes JME, Dewez DF, Gleason JL. Organocatalytic Michael Addition of Indoles to α‐Substituted Enals by Using a Diazepane Carboxylate Catalyst European Journal of Organic Chemistry. 2017: 2637-2640. DOI: 10.1002/Ejoc.201700469 |
0.365 |
|
| 2016 |
Kaldre D, Gleason JL. An Organocatalytic Cope Rearrangement. Angewandte Chemie (International Ed. in English). PMID 27529777 DOI: 10.1002/Anie.201606480 |
0.402 |
|
| 2015 |
Xing S, Gleason JL. A robust synthesis of N-glycolyl muramyl dipeptide via azidonitration/reduction. Organic & Biomolecular Chemistry. 13: 1515-20. PMID 25476476 DOI: 10.1039/C4Ob02147A |
0.433 |
|
| 2014 |
Rycke ND, Denis JDS, Hughes JME, Rosadiuk KA, Gleason JL. Direct Intramolecular Catalytic Enantioselective Alkylation of Oxazolidinone Bromoalkanoate Imides Synlett. 25: 2802-2805. DOI: 10.1055/S-0034-1379236 |
0.47 |
|
| 2013 |
Tiong EA, Rivalti D, Williams BM, Gleason JL. A concise total synthesis of (R)-puraquinonic acid. Angewandte Chemie (International Ed. in English). 52: 3442-5. PMID 23418040 DOI: 10.1002/Anie.201208792 |
0.374 |
|
| 2012 |
Biegasiewicz KF, Ingalsbe ML, St Denis JD, Gleason JL, Ho J, Coote ML, Savage GP, Priefer R. Evaluation of a chiral cubane-based Schiff base ligand in asymmetric catalysis reactions. Beilstein Journal of Organic Chemistry. 8: 1814-8. PMID 23209516 DOI: 10.3762/Bjoc.8.207 |
0.387 |
|
| 2010 |
Ingalsbe ML, Denis JDS, Gleason JL, Savage GP, Priefer R. Synthesis of a Novel ChiralCubane-Based Schiff Base Ligand and Its Application inAsymmetric Nitro-Aldol (Henry) Reactions Synthesis. 2010: 98-102. DOI: 10.1055/S-0029-1217083 |
0.39 |
|
| 2010 |
Ashenhurst JA, Isakovic L, Gleason JL. Application of a [6+4] cycloaddition strategy toward the total synthesis of CP-225,917 Tetrahedron. 66: 368-378. DOI: 10.1016/J.Tet.2009.10.071 |
0.774 |
|
| 2009 |
Tiong EA, Gleason JL. Stereoselective formation of alpha-quaternary stereocenters in the Mannich reaction. Organic Letters. 11: 1725-8. PMID 19354318 DOI: 10.1021/Ol802643K |
0.403 |
|
| 2008 |
Hudon J, Cernak TA, Ashenhurst JA, Gleason JL. Stable 5-substituted cyclopentadienes for the Diels-Alder cycloaddition and their application to the synthesis of palau'amine. Angewandte Chemie (International Ed. in English). 47: 8885-8. PMID 18855951 DOI: 10.1002/Anie.200803344 |
0.763 |
|
| 2008 |
Cernak TA, Gleason JL. Density functional theory guided design of exo-selective dehydroalanine dienophiles for application toward the synthesis of palau'amine. The Journal of Organic Chemistry. 73: 102-10. PMID 18067312 DOI: 10.1021/Jo701866G |
0.735 |
|
| 2008 |
Ashenhurst JA, Gleason JL. CP-225,917 synthetic studies: unusual hydroboration regioselectivity influenced by remote functional groups Tetrahedron Letters. 49: 504-507. DOI: 10.1016/J.Tetlet.2007.11.118 |
0.338 |
|
| 2007 |
Gleason JL, Cernak TA. Synthesis of 5-chloromethylene hydantoins and thiohydantoins Heterocycles. 71: 117-134. DOI: 10.3987/Com-06-10914 |
0.338 |
|
| 2006 |
Arpin A, Manthorpe JM, Gleason JL. A practical chiral bicyclic thioglycolate lactam auxiliary for stereoselective quaternary carbon formation. Organic Letters. 8: 1359-62. PMID 16562891 DOI: 10.1021/Ol060106K |
0.759 |
|
| 2005 |
Cheeseman JD, Corbett AD, Gleason JL, Kazlauskas RJ. Receptor-assisted combinatorial chemistry: thermodynamics and kinetics in drug discovery. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 1708-16. PMID 15565741 DOI: 10.1002/Chem.200400371 |
0.324 |
|
| 2004 |
Ajamian A, Gleason JL. Two birds with one metallic stone: single-pot catalysis of fundamentally different transformations. Angewandte Chemie (International Ed. in English). 43: 3754-60. PMID 15258934 DOI: 10.1002/Anie.200301727 |
0.314 |
|
| 2003 |
Ajamian A, Gleason JL. Cobalt-catalyzed cycloisomerization of 1,6-enynes and allyl propargyl ethers. Organic Letters. 5: 2409-11. PMID 12841742 DOI: 10.1021/Ol034541F |
0.507 |
|
| 2003 |
Burke ED, Lim NK, Gleason JL. Catalytic enantioselective homoaldol reactions using binol titanium(IV) fluoride catalysts Synlett. 2003: 390-392. DOI: 10.1055/S-2003-37122 |
0.392 |
|
| 2003 |
Myers AG, Gleason JL. Asymmetric Synthesis of α‐Amino Acids by the Alkylation of Pseudoephedrine Glycinamide: L‐Allylglycine and N‐Boc‐L‐Allylglycine Organic Syntheses. 76: 57-57. DOI: 10.1002/0471264180.Os076.07 |
0.568 |
|
| 2002 |
Manthorpe JM, Gleason JL. Stereoselective formation of quaternary carbon centers: alkylation of alpha,alpha-disubstituted amide enolates. Angewandte Chemie (International Ed. in English). 41: 2338-41. PMID 12203585 DOI: 10.1002/1521-3773(20020703)41:13<2338::Aid-Anie2338>3.0.Co;2-M |
0.675 |
|
| 2002 |
Cheeseman JD, Corbett AD, Shu R, Croteau J, Gleason JL, Kazlauskas RJ. Amplification of screening sensitivity through selective destruction: theory and screening of a library of carbonic anhydrase inhibitors. Journal of the American Chemical Society. 124: 5692-701. PMID 12010042 DOI: 10.1021/Ja017099+ |
0.332 |
|
| 2002 |
Corbett AD, Gleason JL. Preparation of active esters on solid support for aqueous-phase peptide couplings Tetrahedron Letters. 43: 1369-1372. DOI: 10.1016/S0040-4039(01)02389-9 |
0.339 |
|
| 2001 |
Isakovic L, Ashenhurst JA, Gleason JL. Application of Lewis acid catalyzed tropone [6+4] cycloadditions to the synthesis of the core of CP-225,917. Organic Letters. 3: 4189-92. PMID 11784174 DOI: 10.1021/Ol016814H |
0.781 |
|
| 2001 |
Ajamian A, Gleason JL. Diastereoselective synthesis of 2H,5H-dihydrofurans by cobalt-mediated cycloisomerization of allyl propargyl ethers. Application to poly-THF molecules. Organic Letters. 3: 4161-4164. PMID 11784167 DOI: 10.1021/Ol016768L |
0.494 |
|
| 2001 |
Manthorpe JM, Gleason JL. Stereoselective generation of E- and Z-disubstituted amide enolates. Reductive enolate formation from bicyclic thioglycolate lactams. Journal of the American Chemical Society. 123: 2091-2. PMID 11456846 DOI: 10.1021/Ja0058280 |
0.706 |
|
| 2000 |
Dolaine R, Gleason JL. Diastereoselective formation of 5-vinylcyclopentenes from 1, 6-enynes: cobalt-mediated C-H allylic activation and formal 5-endo-Dig cyclization Organic Letters. 2: 1753-1756. PMID 10880218 DOI: 10.1021/Ol005928A |
0.449 |
|
| 1999 |
and EOM, Gleason JL. Titanium(IV) Triflates in the Catalysis of Homoaldol Reactions Organic Letters. 1: 1643-1645. DOI: 10.1021/Ol991017T |
0.347 |
|
| 1998 |
Myers AG, McKinstry L, Barbay JK, Gleason JL. Practical methodology for the asymmetric synthesis of organofluorine compounds Tetrahedron Letters. 39: 1335-1338. DOI: 10.1016/S0040-4039(98)00152-X |
0.774 |
|
| 1997 |
Myers AG, Yang BH, Chen H, McKinstry L, Kopecky DJ, Gleason JL. Pseudoephedrine as a practical chiral auxiliary for the synthesis of highly enantiomerically enriched carboxylic acids, alcohols, aldehydes, and ketones Journal of the American Chemical Society. 119: 6496-6511. DOI: 10.1021/Ja970402F |
0.672 |
|
| 1997 |
Myers AG, Gleason JL, Yoon T, Kung DW. Highly practical methodology for the synthesis of D- and L-α-amino acids, N-protected α-amino acids, and N-methyl-α-amino acids Journal of the American Chemical Society. 119: 656-673. DOI: 10.1021/Ja9624073 |
0.76 |
|
| 1997 |
Myers AG, McKinstry L, Gleason JL. Synthesis of tertiary alkyl fluoride centers by asymmetric C-C(F) bond formation Tetrahedron Letters. 38: 7037-7040. DOI: 10.1016/S0040-4039(97)01706-1 |
0.636 |
|
| 1996 |
Ireland RE, Gleason JL, Gegnas LD, Highsmith TK. A Total Synthesis of FK-506(1). The Journal of Organic Chemistry. 61: 6856-6872. PMID 11667580 DOI: 10.1021/Jo951646Q |
0.606 |
|
| 1996 |
Myers AG, Gleason JL. A Practical Synthesis of L-Azatyrosine. The Journal of Organic Chemistry. 61: 813-815. PMID 11667015 DOI: 10.1021/Jo9515079 |
0.457 |
|
| 1995 |
Myers AG, Gleason JL, Yoon T. A practical method for the synthesis of D- or L-α-amino acids by the alkylation of (+)- or (-)-pseudoephedrine glycinamide Journal of the American Chemical Society. 117: 8488-8489. DOI: 10.1021/Ja00137A034 |
0.591 |
|
| 1995 |
Myers AG, Yoon T, Gleason JL. A one-step synthesis of pseudoephedrine glycinamide, a versatile precursor for the synthesis of α-amino acids Tetrahedron Letters. 36: 4555-4558. DOI: 10.1016/0040-4039(95)00820-3 |
0.656 |
|
| 1994 |
Myers AG, Yang BH, Chen H, Gleason JL. Use of Pseudoephedrine as a Practical Chiral Auxiliary for Asymmetric Synthesis Journal of the American Chemical Society. 116: 9361-9362. DOI: 10.1021/Ja00099A076 |
0.661 |
|
| 1992 |
Ireland RE, Highsmith TK, Gegnas LD, Gleason JL. Synthesis of the 9,10-acetonide of 9-dihydro-FK-506 Journal of Organic Chemistry. 57: 5071-5073. DOI: 10.1021/Jo00045A013 |
0.616 |
|
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