Year |
Citation |
Score |
2021 |
Cao GM, Hu XL, Liao LL, Yan SS, Song L, Chruma JJ, Gong L, Yu DG. Visible-light photoredox-catalyzed umpolung carboxylation of carbonyl compounds with CO. Nature Communications. 12: 3306. PMID 34083530 DOI: 10.1038/s41467-021-23447-8 |
0.365 |
|
2021 |
Liao LL, Cao GM, Jiang YX, Jin XH, Hu XL, Chruma JJ, Sun GQ, Gui YY, Yu DG. α-Amino Acids and Peptides as Bifunctional Reagents: Carbocarboxylation of Activated Alkenes via Recycling CO. Journal of the American Chemical Society. PMID 33561344 DOI: 10.1021/jacs.0c11896 |
0.404 |
|
2019 |
Ji J, Li Y, Xiao C, Cheng G, Luo K, Gong Q, Zhou D, Chruma JJ, Wu W, Yang C. Supramolecular enantiomeric and structural differentiation of amino acid derivatives with achiral pillar[5]arene homologs. Chemical Communications (Cambridge, England). PMID 31799971 DOI: 10.1039/C9Cc08541F |
0.377 |
|
2019 |
Liu C, Deng C, Yang H, Qian X, Tang S, Poznik M, Chruma JJ. Nickel-Catalyzed Decarboxylative Generation and Asymmetric Allylation of 2-Azaallyl Anions. The Journal of Organic Chemistry. PMID 31328915 DOI: 10.1021/Acs.Joc.9B01293 |
0.591 |
|
2019 |
Tang S, Wei W, Yin D, Poznik M, Chruma JJ. Palladium-Catalyzed Decarboxylative Generation and Propargylation of 2-Azaallyl Anions European Journal of Organic Chemistry. 2019: 3964-3978. DOI: 10.1002/Ejoc.201900537 |
0.541 |
|
2019 |
Wang X, Zeng X, Lin Q, Li M, Walsh PJ, Chruma JJ. Palladium‐Catalysed Decarboxylative Generation and Regiodivergent Prenylation of 2‐Azaallyl Anions Advanced Synthesis & Catalysis. 361: 3751-3757. DOI: 10.1002/Adsc.201900491 |
0.341 |
|
2018 |
Tang S, Zhang X, Sun J, Niu D, Chruma JJ. 2-Azaallyl Anions, 2-Azaallyl Cations, 2-Azaallyl Radicals, and Azomethine Ylides. Chemical Reviews. PMID 30302999 DOI: 10.1021/Acs.Chemrev.8B00349 |
0.317 |
|
2018 |
Wang S, Qian X, Chang Y, Sun J, Xing X, Ballard WF, Chruma JJ. Exploring the Steric and Electronic Factors Governing the Regio- and Enantioselectivity of the Pd-Catalyzed Decarboxylative Generation and Allylation of 2-Azaallyl Anions. The Journal of Organic Chemistry. PMID 29557655 DOI: 10.1021/Acs.Joc.8B00491 |
0.659 |
|
2018 |
Wei X, Wu W, Matsushita R, Yan Z, Zhou D, Chruma JJ, Nishijima M, Fukuhara G, Mori T, Inoue Y, Yang C. Supramolecular Photochirogenesis Driven by Higher-Order Complexation. Enantiodifferentiating Photocyclodimerization of 2-Anthracenecarboxylate to Slipped Cyclodimers via 2:2 Complex with β-Cyclodextrin. Journal of the American Chemical Society. PMID 29437396 DOI: 10.1021/Jacs.7B12085 |
0.3 |
|
2018 |
Chruma JJ, Cullen DJ, Bowman L, Toy PH. Polyunsaturated fatty acid amides from the Zanthoxylum genus - from culinary curiosities to probes for chemical biology. Natural Product Reports. PMID 29299588 DOI: 10.1039/C7Np00044H |
0.351 |
|
2018 |
Wang Q, Poznik M, Li M, Walsh PJ, Chruma JJ. 2-Azaallyl Anions as Light-Tunable Super-Electron-Donors: Coupling with Aryl Fluorides, Chlorides, and Bromides Advanced Synthesis & Catalysis. 360: 2854-2868. DOI: 10.1002/Adsc.201800396 |
0.346 |
|
2017 |
Li M, Berritt S, Matuszewski L, Deng G, Pascual-Escudero A, Panetti GB, Poznik M, Yang X, Chruma JJ, Walsh PJ. Transition-Metal-Free Radical C(sp3)-C(sp2) and C(sp3)-C(sp3) Coupling Enabled by 2-Azaallyls as Super-Electron-Donors and Coupling-Partners. Journal of the American Chemical Society. PMID 29019654 DOI: 10.1021/Jacs.7B09394 |
0.414 |
|
2017 |
Yao J, Wu W, Liang W, Feng Y, Zhou D, Chruma JJ, Fukuhara G, Mori T, Inoue Y, Yang C. Temperature-Driven Planar Chirality Switching of a Pillar[5]arene-Based Molecular Universal Joint. Angewandte Chemie (International Ed. in English). PMID 28493649 DOI: 10.1002/Anie.201702542 |
0.33 |
|
2017 |
Yan Z, Huang Q, Liang W, Yu X, Zhou D, Wu W, Chruma JJ, Yang C. Enantiodifferentiation in the Photoisomerization of (Z,Z)-1,3-Cyclooctadiene in the Cavity of γ-Cyclodextrin-Curcubit[6]uril-Wheeled [4]Rotaxanes with an Encapsulated Photosensitizer. Organic Letters. PMID 28133969 DOI: 10.1021/Acs.Orglett.7B00057 |
0.312 |
|
2016 |
Xiang M, Wu Y, Burke JP, Chruma JJ. High pi-Facial and exo-Selectivity for the Intramolecular Diels-Alder Cycloaddition of Dodeca-3,9,11-trien-5-one Precursors to 2-epi-Symbioimine and Related Compounds. The Journal of Organic Chemistry. PMID 27563727 DOI: 10.1021/Acs.Joc.6B01677 |
0.406 |
|
2015 |
Tang S, Park JY, Yeagley AA, Sabat M, Chruma JJ. Decarboxylative Generation of 2-Azaallyl Anions: 2-Iminoalcohols via a Decarboxylative Erlenmeyer Reaction. Organic Letters. 17: 2042-5. PMID 25885173 DOI: 10.1021/Acs.Orglett.5B00107 |
0.78 |
|
2014 |
Qian X, Ji P, He C, Zirimwabagabo JO, Archibald MM, Yeagley AA, Chruma JJ. Palladium-catalyzed decarboxylative generation and asymmetric allylation of α-imino anions. Organic Letters. 16: 5228-31. PMID 25243507 DOI: 10.1021/Ol502693R |
0.757 |
|
2012 |
Li Z, Jiang YY, Yeagley AA, Bour JP, Liu L, Chruma JJ, Fu Y. Mechanism of the Pd-catalyzed decarboxylative allylation of α-imino esters: decarboxylation via free carboxylate ion. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 14527-38. PMID 23002017 DOI: 10.1002/Chem.201201425 |
0.806 |
|
2011 |
Burke JP, Sabat M, Myers WH, Chruma JJ. Unexpected exo selectivity for an intramolecular Diels-Alder reaction involving a doubly-activated δ-pentenolide dienophile Tetrahedron Asymmetry. 22: 31-35. DOI: 10.1016/J.Tetasy.2010.12.018 |
0.419 |
|
2010 |
Burke JP, Sabat M, Iovan DA, Myers WH, Chruma JJ. Exploring the original proposed biosynthesis of (+)-symbioimine: remote exocyclic stereocontrol in a type I IMDA reaction. Organic Letters. 12: 3192-5. PMID 20550217 DOI: 10.1021/Ol101141A |
0.358 |
|
2010 |
Fields WH, Chruma JJ. Palladium-catalyzed decarboxylative benzylation of diphenylglycinate imines. Organic Letters. 12: 316-9. PMID 20000671 DOI: 10.1021/Ol902651J |
0.592 |
|
2009 |
Yeagley AA, Lowder MA, Chruma JJ. Tandem C-C bond-forming processes: interception of the pd-catalyzed decarboxylative allylation of allyl diphenylglycinate imines with activated olefins. Organic Letters. 11: 4022-5. PMID 19658425 DOI: 10.1021/Ol901745X |
0.805 |
|
2009 |
Chruma JJ, Moon SJ, Sanford WE. Azaphilone α-Bromoacetates (AzαBs): Fluorescent linchpin reagents for the inter- and intramolecular cross-linkage of primary amines to thiols Letters in Organic Chemistry. 6: 367-371. DOI: 10.2174/157017809788681428 |
0.339 |
|
2008 |
Fields WH, Khan AK, Sabat M, Chruma JJ. One-pot tandem decarboxylative allylation-Heck cyclization of allyl diphenylglycinate imines: rapid access to polyfunctionalized 1-aminoindanes. Organic Letters. 10: 5131-4. PMID 18956870 DOI: 10.1021/Ol801986M |
0.727 |
|
2007 |
Yeagley AA, Chruma JJ. C-C bond-forming reactions via Pd-mediated decarboxylative alpha-imino anion generation. Organic Letters. 9: 2879-82. PMID 17580888 DOI: 10.1021/Ol071080F |
0.791 |
|
2007 |
Yeagley AA, Chruma JJ. C—C Bond-Forming Reactions via Pd-Mediated Decarboxylative α-Imino Anion Generation. Cheminform. 38. DOI: 10.1002/chin.200747075 |
0.793 |
|
2005 |
Chruma JJ, Liu L, Zhou W, Breslow R. Hydrophobic and electronic factors in the design of dialkylglycine decarboxylase mimics. Bioorganic & Medicinal Chemistry. 13: 5873-83. PMID 15953728 DOI: 10.1016/J.Bmc.2005.05.019 |
0.539 |
|
2005 |
Zhou W, Yerkes N, Chruma JJ, Liu L, Breslow R. Chiral polyamines from reduction of polypeptides: asymmetric pyridoxamine-mediated transaminations. Bioorganic & Medicinal Chemistry Letters. 15: 1351-5. PMID 15713385 DOI: 10.1016/J.Bmcl.2005.01.021 |
0.561 |
|
2004 |
Liu L, Zhou W, Chruma J, Breslow R. Transamination reactions with multiple turnovers catalyzed by hydrophobic pyridoxamine cofactors in the presence of polyethylenimine polymers Journal of the American Chemical Society. 126: 8136-8137. PMID 15225053 DOI: 10.1021/Ja048671A |
0.55 |
|
2004 |
Smith AB, Chruma JJ, Han Q, Barbosa J. Complestatin synthetic studies; the effect of the amino acid configuration on peptide backbone conformation in the common western BCD macrocycle. Bioorganic & Medicinal Chemistry Letters. 14: 1697-702. PMID 15026053 DOI: 10.1016/J.Bmcl.2004.01.056 |
0.498 |
|
1999 |
Polt R, Sames D, Chruma J. Glycosidase inhibitors: Synthesis of enantiomerically pure aza-sugars from Schiff base amino esters via tandem reduction-alkenylation and osmylation Journal of Organic Chemistry. 64: 6147-6158. DOI: 10.1021/Jo9820115 |
0.658 |
|
1997 |
Chruma JJ, Sames D, Polt R. General method for the synthesis of N-methyl amino acids and N-alkyl amino esters from O'Donnell's Schiff bases Tetrahedron Letters. 38: 5085-5086. DOI: 10.1016/S0040-4039(97)01132-5 |
0.631 |
|
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