Year |
Citation |
Score |
2023 |
Peck AM, Brewer M. Lewis-Acid-Catalyzed Oxa-Michael Addition to Give α-Diazo-β-alkoxy Carbonyls and Tetrahydro-3-furo[3,4-]pyrazoles. Organic Letters. PMID 37022675 DOI: 10.1021/acs.orglett.3c00723 |
0.637 |
|
2022 |
Li J, Remington JM, Liao C, Parsons RL, Schneebeli S, Braas KM, May V, Brewer M. GPCR Intracellular Loop Regulation of Beta-Arrestin-Mediated Endosomal Signaling Dynamics. Journal of Molecular Neuroscience : Mn. PMID 35538393 DOI: 10.1007/s12031-022-02016-8 |
0.476 |
|
2020 |
Fang J, Howard EM, Brewer M. A conjugate addition approach to diazo-containing scaffolds with β quaternary centers. Angewandte Chemie (International Ed. in English). PMID 32365265 DOI: 10.1002/Anie.202004557 |
0.656 |
|
2019 |
Hensinger MJ, Dodge NJ, Brewer M. Substituted α-Alkylidene Cyclopentenones via the Intramolecular Reaction of Vinyl Cations with Alkenes. Organic Letters. PMID 31873030 DOI: 10.1021/Acs.Orglett.9B04255 |
0.681 |
|
2019 |
Cleary SE, Hensinger MJ, Qin ZX, Hong X, Brewer M. Migratory Aptitudes in Rearrangements of Destabilized Vinyl Cations. The Journal of Organic Chemistry. PMID 31747287 DOI: 10.1021/Acs.Joc.9B02130 |
0.671 |
|
2019 |
Liao C, de Molliens MP, Schneebeli ST, Brewer M, Song G, Chatenet D, Braas KM, May V, Li J. Targeting the PAC1 Receptor for Neurological and Metabolic Disorders. Current Topics in Medicinal Chemistry. PMID 31284862 DOI: 10.2174/1568026619666190709092647 |
0.53 |
|
2019 |
Cleary SE, Li X, Yang LC, Houk KN, Hong X, Brewer M. Reactivity Profiles of Diazo Amides, Esters, and Ketones in Transition-Metal-Free C-H Insertion Reactions. Journal of the American Chemical Society. PMID 30758200 DOI: 10.1021/Jacs.8B12420 |
0.677 |
|
2018 |
Fang J, Brewer M. Intramolecular Vinylation of Aryl Rings by Vinyl Cations. Organic Letters. PMID 30426753 DOI: 10.1021/Acs.Orglett.8B03054 |
0.682 |
|
2018 |
Dhakal R, Ivancic M, Brewer M. Two-Step Sequence of Cycloadditions Gives Structurally Complex Tetracyclic 1,2,3,4-Tetrahydrocinnoline Products. The Journal of Organic Chemistry. PMID 29781614 DOI: 10.1021/Acs.Joc.8B00683 |
0.792 |
|
2017 |
Cleary SE, Hensinger MJ, Brewer M. Remote C-H insertion of vinyl cations leading to cyclopentenones. Chemical Science. 8: 6810-6814. PMID 29147505 DOI: 10.1039/C7Sc02768K |
0.697 |
|
2017 |
Liao C, Zhao X, Brewer M, May V, Li J. Conformational Transitions of the Pituitary Adenylate Cyclase-Activating Polypeptide Receptor, a Human Class B GPCR. Scientific Reports. 7: 5427. PMID 28710390 DOI: 10.1038/S41598-017-05815-X |
0.535 |
|
2017 |
Al-Bataineh N, Houk KN, Brewer M, Hong X. (2 + 1)-Cycloaddition Reactions Give Further Evidence of the Nitrenium-like Character of 1-Aza-2-azoniaallene Salts. The Journal of Organic Chemistry. PMID 28318256 DOI: 10.1021/Acs.Joc.7B00407 |
0.696 |
|
2016 |
Dhakal RC, Brewer M. Intramolecular (4 + 2) cycloaddition of aryl-1-aza-2-azoniaallene salts: A practical approach to highly sterically-congested polycyclic protonated azomethine imines. Tetrahedron. 72: 3718-3728. PMID 32071487 DOI: 10.1016/J.Tet.2016.03.037 |
0.814 |
|
2016 |
Giampa GM, Fang J, Brewer M. A Route to the C,D,E Ring System of the Aspidosperma Alkaloids. Organic Letters. PMID 27500799 DOI: 10.1021/Acs.Orglett.6B01674 |
0.686 |
|
2015 |
Hong X, Bercovici DA, Yang Z, Al-Bataineh N, Srinivasan R, Dhakal RC, Houk KN, Brewer M. Mechanism and Dynamics of Intramolecular C-H Insertion Reactions of 1-Aza-2-azoniaallene Salts. Journal of the American Chemical Society. 137: 9100-7. PMID 26151292 DOI: 10.1021/Jacs.5B04474 |
0.788 |
|
2015 |
Collins N, Brewer M. Development of a Clinically Applicable Protocol for Assessment of Hypoxic Response Through Measurement of the Endogenous Gasotransmitter Hydrogen Sulfide in Human Plasma. Journal of Neurosurgical Anesthesiology. 27: 257-61. PMID 25514494 DOI: 10.1097/Ana.0000000000000150 |
0.53 |
|
2015 |
Hong X, Bercovici DA, Yang Z, Al-Bataineh N, Srinivasan R, Dhakal RC, Houk KN, Brewer M. Mechanism and Dynamics of Intramolecular C-H Insertion Reactions of 1-Aza-2-azoniaallene Salts Journal of the American Chemical Society. 137: 9100-9107. DOI: 10.1021/jacs.5b04474 |
0.768 |
|
2015 |
Dhakal RC, Brewer M. Intramolecular (4+2) cycloaddition of aryl-1-aza-2-azoniaallene salts: A practical approach to highly sterically-congested polycyclic protonated azomethine imines Tetrahedron. DOI: 10.1016/j.tet.2016.03.037 |
0.817 |
|
2014 |
Hong X, Liang Y, Brewer M, Houk KN. How tethers control the chemo- and regioselectivities of intramolecular cycloadditions between aryl-1-aza-2-azoniaallenes and alkenes. Organic Letters. 16: 4260-3. PMID 25058856 DOI: 10.1021/Ol501958S |
0.648 |
|
2014 |
Bayir A, Brewer M. Fragmentation of bicyclic γ-silyloxy-β-hydroxy-α-diazolactones as an approach to ynolides. The Journal of Organic Chemistry. 79: 6037-46. PMID 24922068 DOI: 10.1021/Jo500634D |
0.642 |
|
2014 |
Jabre ND, Watanabe T, Brewer M. Formal and total synthesis of (±)-cycloclavine. Tetrahedron Letters. 56: 197-199. PMID 24511164 DOI: 10.1016/J.Tetlet.2013.10.152 |
0.635 |
|
2014 |
Bayir A, Brewer M. ChemInform Abstract: Fragmentation of Bicyclic γ-Silyloxy-β-hydroxy-α-diazolactones as an Approach to Ynolides. Cheminform. 45: no-no. DOI: 10.1002/chin.201452175 |
0.532 |
|
2014 |
Jabre ND, Watanabe T, Brewer M. ChemInform Abstract: Formal and Total Synthesis of (.+-.)-Cycloclavine (I). Cheminform. 45: no-no. DOI: 10.1002/chin.201421229 |
0.552 |
|
2013 |
Bercovici DA, Ogilvie JM, Tsvetkov N, Brewer M. Intramolecular polar [4(⊕)+2] cycloadditions of aryl-1-aza-2-azoniaallene salts: unprecedented reactivity leading to polycyclic protonated azomethine imines. Angewandte Chemie (International Ed. in English). 52: 13338-41. PMID 24218159 DOI: 10.1002/Anie.201306553 |
0.819 |
|
2013 |
Zhang Z, Giampa GM, Draghici C, Huang Q, Brewer M. Synthesis of demissidine by a ring fragmentation 1,3-dipolar cycloaddition approach. Organic Letters. 15: 2100-3. PMID 23586838 DOI: 10.1021/Ol4004993 |
0.802 |
|
2013 |
Al-Bataineh NQ, Brewer M. ChemInform Abstract: Iodine(III)-Mediated Bicyclic Diazenium Salt Formation. Cheminform. 44: no-no. DOI: 10.1002/chin.201302095 |
0.551 |
|
2012 |
Jabre ND, Brewer M. Stereoelectronic effects in the fragmentation of γ-silyloxy-β-hydroxy-α-diazocarbonyl compounds. The Journal of Organic Chemistry. 77: 9910-4. PMID 23066902 DOI: 10.1021/Jo301944T |
0.606 |
|
2012 |
Bercovici DA, Brewer M. Stereospecific intramolecular C-H amination of 1-aza-2-azoniaallene salts. Journal of the American Chemical Society. 134: 9890-3. PMID 22680985 DOI: 10.1021/Ja303054C |
0.821 |
|
2012 |
Tsvetkov NP, Bayir A, Schneider S, Brewer M. A ring fragmentation approach to medium-sized cyclic 2-alkynones. Organic Letters. 14: 264-7. PMID 22132946 DOI: 10.1021/Ol2030422 |
0.635 |
|
2012 |
Al-Bataineh NQ, Brewer M. Iodine(III)-mediated bicyclic diazenium salt formation Tetrahedron Letters. 53: 5411-5413. DOI: 10.1016/J.Tetlet.2012.07.116 |
0.623 |
|
2012 |
Bercovici DA, Brewer M. ChemInform Abstract: Stereospecific Intramolecular C-H Amination of 1-Aza-2-azoniaallene Salts. Cheminform. 43: no-no. DOI: 10.1002/chin.201245144 |
0.772 |
|
2010 |
Wyman J, Javed MI, Al-Bataineh N, Brewer M. Synthetic approaches to bicyclic diazenium salts. The Journal of Organic Chemistry. 75: 8078-87. PMID 21067195 DOI: 10.1021/Jo101706H |
0.66 |
|
2010 |
Bayir A, Draghici C, Brewer M. Preparation of tethered aldehyde ynoates and ynones by ring fragmentation of cyclic gamma-oxy-beta-hydroxy-alpha-diazo carbonyls. The Journal of Organic Chemistry. 75: 296-302. PMID 20020697 DOI: 10.1021/Jo902405F |
0.611 |
|
2010 |
Bayir A, Draghici C, Brewer M. ChemInform Abstract: Preparation of Tethered Aldehyde Ynoates and Ynones by Ring Fragmentation of Cyclic γ-Oxy-β-hydroxy-α-diazo Carbonyls. Cheminform. 41. DOI: 10.1002/chin.201018055 |
0.586 |
|
2009 |
Draghici C, Huang Q, Brewer M. An efficient synthetic approach to polycyclic 2,5-dihydropyrroles from alpha-silyloxy ketones. The Journal of Organic Chemistry. 74: 8410-3. PMID 19827755 DOI: 10.1021/Jo901978Y |
0.78 |
|
2009 |
Javed MI, Wyman JM, Brewer M. Synthesis of fused and bridged bicyclic diazenium salts by intramolecular cycloaddition. Organic Letters. 11: 2189-92. PMID 19371074 DOI: 10.1021/Ol900502S |
0.66 |
|
2009 |
Wyman JM, Jochum S, Brewer M. ChemInform Abstract: Chlorodimethylsulfonium Chloride Mediated Formation of Phenyl-α-chloroazoalkanes. Cheminform. 40. DOI: 10.1002/chin.200915066 |
0.565 |
|
2008 |
Harriman GC, Brewer M, Bennett R, Kuhn C, Bazin M, Larosa G, Skerker P, Cochran N, Gallant D, Baxter D, Picarella D, Jaffee B, Luly JR, Briskin MJ. Selective cell adhesion inhibitors: Barbituric acid based alpha4beta7--MAdCAM inhibitors. Bioorganic & Medicinal Chemistry Letters. 18: 2509-12. PMID 18331794 DOI: 10.1016/j.bmcl.2007.07.068 |
0.47 |
|
2008 |
Draghici C, Brewer M. Lewis acid promoted carbon-carbon bond cleavage of gamma-silyloxy-beta-hydroxy-alpha-diazoesters. Journal of the American Chemical Society. 130: 3766-7. PMID 18321118 DOI: 10.1021/Ja801004D |
0.581 |
|
2008 |
Wyman JM, Jochum S, Brewer M. Chlorodimethylsulfonium chloride-mediated formation of phenyl-α- chloroazoalkanes Synthetic Communications. 38: 3623-3630. DOI: 10.1080/00397910802179961 |
0.663 |
|
2008 |
Draghici C, Brewer M. ChemInform Abstract: Lewis Acid Promoted Carbon-Carbon Bond Cleavage of γ-Silyloxy-β-hydroxy-α-diazoesters. Cheminform. 39. DOI: 10.1002/chin.200832034 |
0.528 |
|
2007 |
Javed MI, Brewer M. Diazo preparation via dehydrogenation of hydrazones with "activated" DMSO. Organic Letters. 9: 1789-92. PMID 17408280 DOI: 10.1021/Ol070515W |
0.61 |
|
2007 |
Brewer M. Conversion of Hydrazones to Alkyl Chlorides under Swern Oxidation Conditions. Cheminform. 38. DOI: 10.1002/chin.200706047 |
0.506 |
|
2006 |
Brewer M. Conversion of hydrazones to alkyl chlorides under Swern oxidation conditions Tetrahedron Letters. 47: 7731-7733. DOI: 10.1016/J.Tetlet.2006.08.120 |
0.604 |
|
2004 |
Brewer M, James CA, Rich DH. Synthesis of a tripeptide derivative containing the gln-arg hydroxyethylene dipeptide isostere. Organic Letters. 6: 4779-82. PMID 15575684 DOI: 10.1021/Ol047880X |
0.673 |
|
2003 |
Oost T, Sukonpan C, Brewer M, Goodnough M, Tepp W, Johnson EA, Rich DH. Design and synthesis of substrate-based inhibitors of botulinum neurotoxin type B metalloprotease. Biopolymers. 71: 602-19. PMID 14991672 DOI: 10.1002/Bip.10590 |
0.752 |
|
2002 |
Brewer M, Oost T, Sukonpan C, Pereckas M, Rich DH. Sequencing hydroxyethylamine-containing peptides via Edman degradation. Organic Letters. 4: 3469-72. PMID 12323046 DOI: 10.1021/Ol026590I |
0.737 |
|
2001 |
Brewer M, Rich DH. Synthesis of a tripeptide derivative containing the Phe-Arg hydroxyethylene dipeptide isostere. Organic Letters. 3: 945-8. PMID 11263922 DOI: 10.1021/ol015612i |
0.709 |
|
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