Year |
Citation |
Score |
2021 |
Monsen PJ, Luzzio FA. Chemoenzymatic route to stereodefined 2-(azidophenyl)oxazolines for click chemistry. Tetrahedron Letters. 63. PMID 33716327 DOI: 10.1016/j.tetlet.2020.152717 |
0.811 |
|
2020 |
Monsen PJ, Luzzio FA. Applicability of aluminum amalgam to the reduction of arylnitro groups. Tetrahedron Letters. 61. PMID 33299259 DOI: 10.1016/j.tetlet.2020.152575 |
0.788 |
|
2019 |
Patil PC, Tan J, Demuth DR, Luzzio FA. 'Second-generation' 1,2,3-triazole-based inhibitors of adherence to oral streptococci and biofilm formation. Medchemcomm. 10: 268-279. PMID 30881614 DOI: 10.1039/C8Md00405F |
0.361 |
|
2019 |
Ronnebaum JM, Luzzio FA. DAST-mediated preparation of N-substituted 3-alkoxyisoindolinones Arkivoc. 2019: 298-306. DOI: 10.24820/Ark.5550190.P010.809 |
0.761 |
|
2019 |
Monsen PJ, Luzzio FA. Isolation and Derivatization of Sucralose from an Artificial Sweetener to Provide a Hands-On Laboratory Experiment Emphasizing Synthesis and Purification Journal of Chemical Education. 96: 992-997. DOI: 10.1021/Acs.Jchemed.8B00413 |
0.746 |
|
2018 |
Patil PC, Luzzio FA. Alternate pathway for the click reaction of 2-(2-azidophenyl)-4,5-diaryloxazoles. Tetrahedron Letters. 59: 3458-3460. PMID 31537949 DOI: 10.1016/J.Tetlet.2018.07.062 |
0.435 |
|
2018 |
Monsen PJ, Luzzio FA. Antiangiogenic Activity and Chemical Derivatization of the Neurotoxic Acetogenin Annonacin Isolated from Asimina triloba. Journal of Natural Products. PMID 30028612 DOI: 10.1021/Acs.Jnatprod.8B00284 |
0.754 |
|
2017 |
Patil PC, Luzzio FA. Unnatural Amino Acid Derivatives through Click Chemistry: Synthesis of Triazolylalanine Analogues. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 28: 1729-1732. PMID 29904233 DOI: 10.1055/S-0036-1588510 |
0.488 |
|
2017 |
Patil PC, Luzzio FA, Ronnebaum JM. Selective alkylation/oxidation of N-substituted isoindolinone derivatives: synthesis of N-phthaloylated natural and unnatural α-amino acid analogues. Tetrahedron Letters. 58: 3730-3733. PMID 29230073 DOI: 10.1016/J.Tetlet.2017.08.032 |
0.774 |
|
2017 |
Patil PC, Luzzio FA. m-Chloroperbenzoic acid-oxchromium (VI)-mediated cleavage of 2,4,5-trisubstituted oxazoles. Tetrahedron Letters. 58: 1280-1282. PMID 28970642 DOI: 10.1016/J.Tetlet.2017.02.027 |
0.429 |
|
2017 |
Patil PC, Luzzio FA. The intramolecular click reaction using 'carbocontiguous' precursors. Tetrahedron. 73: 4206-4213. PMID 28943665 DOI: 10.1016/J.Tet.2016.11.016 |
0.459 |
|
2017 |
Luzzio FA, Monsen PJ. Selective fluorination of natural products Arkivoc. 2017: 117-147. DOI: 10.24820/Ark.5550190.P009.917 |
0.75 |
|
2016 |
Patil PC, Luzzio FA. Synthesis of Extended Oxazoles III: Reactions of 2-(Phenylsulfonyl)methyl-4,5-diaryloxazoles. The Journal of Organic Chemistry. PMID 27441569 DOI: 10.1021/Acs.Joc.6B01280 |
0.433 |
|
2016 |
Patil PC, Luzzio FA. Synthesis of extended oxazoles II: Reaction manifold of 2-(halomethyl)-4,5-diaryloxazoles. Tetrahedron Letters. 57: 757-759. PMID 26989270 DOI: 10.1016/J.Tetlet.2016.01.016 |
0.468 |
|
2016 |
Ronnebaum JM, Luzzio FA. Synthesis of 1,2,3-triazole ‘click’ analogues of thalidomide Tetrahedron. 72: 6136-6141. DOI: 10.1016/J.Tet.2016.07.019 |
0.788 |
|
2015 |
Patil PC, Luzzio FA, Demuth DR. Oxazoles for click chemistry II: synthesis of extended heterocyclic scaffolds. Tetrahedron Letters. 56: 3039-3041. PMID 26120210 DOI: 10.1016/J.Tetlet.2014.11.014 |
0.478 |
|
2012 |
Loner CM, Luzzio FA, Demuth DR. Preparation of azidoaryl- and azidoalkyloxazoles for click chemistry. Tetrahedron Letters. 53: 5641-5644. PMID 25960576 DOI: 10.1016/J.Tetlet.2012.08.032 |
0.413 |
|
2012 |
Luzzio FA. 1,3-Oxidative transpositions of allylic alcohols in organic synthesis Tetrahedron. 68: 5323-5339. DOI: 10.1016/J.Tet.2012.04.045 |
0.361 |
|
2011 |
Luzzio FA, Okoromoba OE. Tandem Henry/oxa-Michael route to the 1,3-disubstituted-1,3-dihydrobenzo[c] furan system Tetrahedron Letters. 52: 6530-6533. DOI: 10.1016/J.Tetlet.2011.09.123 |
0.448 |
|
2011 |
Dempster RK, Luzzio FA. A direct arylation-oxidation route to 3-arylisoindolinone inhibitors of MDM2-p53 interaction Tetrahedron Letters. 52: 4992-4995. DOI: 10.1016/J.Tetlet.2011.07.076 |
0.442 |
|
2010 |
LUZZIO FA, ZACHERL DP. ChemInform Abstract: Alkylation and Annulation of 3-(Phenylsulfonyl)-2-alkyl-2,3-dihydroisoindol-1-ones. Cheminform. 29: no-no. DOI: 10.1002/chin.199829134 |
0.302 |
|
2010 |
LUZZIO FA, MOORE WJ. ChemInform Abstract: Oxidative Rearrangement of Sulfur-Containing Tertiary Allylic Alcohols: Synthesis of 2-Cycloalkenones Bearing 3-((Phenylthio)methyl) and 3-(2- Alkyl-1,3-dithian-2-yl) Substituents. Cheminform. 24: no-no. DOI: 10.1002/chin.199337118 |
0.615 |
|
2010 |
LUZZIO FA, MOORE WJ. ChemInform Abstract: Ultrasound in Oxochromium(VI)-Mediated Transformations. Part 2. Ultrasound-Mediated Preparation and Application of Chromyl Chloride. Cheminform. 24: no-no. DOI: 10.1002/chin.199321097 |
0.518 |
|
2009 |
Luzzio FA, Chen J. Synthetically useful Brønsted acid-promoted arylbenzyl ether --> o-benzylphenol rearrangements. The Journal of Organic Chemistry. 74: 5629-32. PMID 19518072 DOI: 10.1021/Jo9007833 |
0.361 |
|
2009 |
Luzzio FA, Wlodarczyk MT. Preparation of benzoheterocyclic carbaldeydes Tetrahedron Letters. 50: 580-583. DOI: 10.1016/J.Tetlet.2008.11.066 |
0.475 |
|
2008 |
Luzzio FA, Chen J. Efficient preparation and processing of the 4-methoxybenzyl (PMB) group for phenolic protection using ultrasound. The Journal of Organic Chemistry. 73: 5621-4. PMID 18549286 DOI: 10.1021/Jo800577F |
0.433 |
|
2007 |
Luzzio FA, Wlodarczyk MT, Duveau DY, Chen J. Preparation of β-phenylnitroethanes having electron-donating aryl substitution Tetrahedron Letters. 48: 6704-6708. DOI: 10.1016/J.Tetlet.2007.07.098 |
0.734 |
|
2006 |
Luzzio FA, Ott JP, Duveau DY. Radical-induced cyclopentannulation of Henry (nitroaldol)-derived intermediates. The Journal of Organic Chemistry. 71: 5027-30. PMID 16776541 DOI: 10.1021/Jo0605546 |
0.737 |
|
2006 |
Luzzio FA, Duveau DY, Figg WD. A chiral pool approach toward the synthesis of thalidomide metabolites Heterocycles. 70: 321-334. DOI: 10.3987/Com-06-S(W)28 |
0.758 |
|
2005 |
Luzzio FA, Duveau DY, Lepper ER, Figg WD. Synthesis of racemic cis-5-hydroxy-3-phthalimidoglutarimide. A metabolite of thalidomide isolated from human plasma. The Journal of Organic Chemistry. 70: 10117-20. PMID 16292851 DOI: 10.1021/Jo0514772 |
0.789 |
|
2004 |
Luzzio FA. The Oxidation of Alcohols by Modified Oxochromium(VI)–Amine Reagents Organic Reactions. 1-221. DOI: 10.1002/0471264180.Or053.01 |
0.417 |
|
2003 |
Luzzio FA, Mayorov AV, Ng SS, Kruger EA, Figg WD. Thalidomide metabolites and analogues. 3. Synthesis and antiangiogenic activity of the teratogenic and TNFalpha-modulatory thalidomide analogue 2-(2,6-dioxopiperidine-3-yl)phthalimidine. Journal of Medicinal Chemistry. 46: 3793-9. PMID 12930142 DOI: 10.1021/Jm020079D |
0.698 |
|
2003 |
Luzzio FA, Mayorov AV. Palladium(0)-mediated preparation of trans-4-substituted-1- (phthalimido)-2-cyclopentenes Synlett. 532-536. DOI: 10.1055/S-2003-37516 |
0.689 |
|
2002 |
Luzzio FA, Duveau DY. Enzymatic resolution of the 1,3,3-trimethyl-2-oxabicyclo[2.2.2]octane (1,8-cineole) system Tetrahedron Asymmetry. 13: 1173-1180. DOI: 10.1016/S0957-4166(02)00313-0 |
0.748 |
|
2001 |
Luzzio FA. The Henry reaction: Recent examples Tetrahedron. 57: 915-945. DOI: 10.1016/S0040-4020(00)00965-0 |
0.311 |
|
2000 |
Luzzio FA, Thomas EM, Figg WD. Thalidomide metabolites and analogs. Part 2: Cyclic derivatives of 2-N-phthalimido-2S,3S (3-hydroxy) ornithine Tetrahedron Letters. 41: 7151-7155. DOI: 10.1016/S0040-4039(00)01204-1 |
0.434 |
|
2000 |
Luzzio FA, Mayorov AV, Figg WD. Thalidomide metabolites. Part 1: Derivatives of (+)-2-(N-phthalimido)- γ-hydroxyglutamic acid Tetrahedron Letters. 41: 2275-2278. DOI: 10.1016/S0040-4039(00)00160-X |
0.712 |
|
2000 |
Luzzio FA, Fitch RW. A Rearrangement Route to Fenvaleric Acid Advanced Synthesis and Catalysis. 342: 498-501. DOI: 10.1002/1521-3897(200006)342:5<498::Aid-Prac498>3.0.Co;2-G |
0.746 |
|
1999 |
Luzzio FA, Fitch RW. Formal Synthesis of (+)- and (-)-Perhydrohistrionicotoxin: A "Double Henry"/Enzymatic Desymmetrization Route to the Kishi Lactam(1). The Journal of Organic Chemistry. 64: 5485-5493. PMID 11674611 DOI: 10.1021/Jo990293I |
0.762 |
|
1999 |
Luzzio FA, Mayorov AV, Menes ME, Champion WL. Asymmetric Synthesis of 4′-Methyl-2′,3′-dideoxynucleosides Nucleosides and Nucleotides. 18: 1977-1984. DOI: 10.1080/07328319908044858 |
0.397 |
|
1999 |
Luzzio FA, Fitch RW. Formal synthesis of (+)- and (-)-perhydrohistrionicotoxin: A 'double Henry'/enzymatic desymmetrization route to the Kishi lactam Journal of Organic Chemistry. 64: 5485-5493. DOI: 10.1021/jo990293i |
0.747 |
|
1999 |
Luzzio FA, Fitch RW, Moore WJ, Mudd KJ. A Facile Oxidation of Alcohols Using Pyridinium Chlorochromate/Silica Gel Journal of Chemical Education. 76: 974-975. DOI: 10.1021/Ed076P974 |
0.736 |
|
1999 |
Luzzio FA, Piatt Zacherl DA, Figg WD. A facile scheme for phthalimide ⇆ phthalimidine conversion Tetrahedron Letters. 40: 2087-2090. DOI: 10.1016/S0040-4039(99)00152-5 |
0.465 |
|
1999 |
Luzzio FA, Bobb RA. Organomercury/aluminum-mediated acylative cleavage of cyclic ethers Tetrahedron. 55: 1851-1858. DOI: 10.1016/S0040-4020(98)01226-5 |
0.422 |
|
1999 |
Luzzio FA, Mayorov AV, Menes ME, Champion WL. Asymmetric synthesis of 4'-methyl-2',3'-dideoxynucleosides Nucleosides and Nucleotides. 18: 1977-1984. |
0.669 |
|
1998 |
Luzzio FA, Zacherl DP. Alkylation and annulation of 3-(phenylsulfonyl)-2-alkyl-2,3- dihydroisoindol-1-ones Tetrahedron Letters. 39: 2285-2288. DOI: 10.1016/S0040-4039(98)00293-7 |
0.5 |
|
1997 |
Fitch RW, Luzzio FA. Ultrasound in natural products synthesis: Applications to the synthesis of histrionicotoxin via nitroalkanal acetals Ultrasonics Sonochemistry. 4: 99-107. PMID 11237051 DOI: 10.1016/S1350-4177(97)00006-0 |
0.734 |
|
1997 |
Luzzio FA, Bobb RA. 2,2'-Bipyridinium chlorochromate/m-chloroperbenzoic acid-mediated cleavage of cyclic acetals to hydroxyesters Tetrahedron Letters. 38: 1733-1736. DOI: 10.1016/S0040-4039(97)00203-7 |
0.315 |
|
1995 |
Moore WJ, Luzzio FA. Synthetic studies directed toward the liposidomycins: Preparation and reactions of serine-derived epoxides Tetrahedron Letters. 36: 6599-6602. DOI: 10.1016/00404-0399(50)1349-M |
0.681 |
|
1994 |
Luzzio FA, Menes ME. A facile route to pyrimidine-based nucleoside olefins: Application to the synthesis of d4T (stavudine) Journal of Organic Chemistry. 59: 7267-7272. DOI: 10.1021/Jo00103A017 |
0.438 |
|
1994 |
Fitch RW, Luzzio FA. The aluminum amalgam reduction of 2-nitroalkanols promoted by ultrasound Tetrahedron Letters. 35: 6013-6016. DOI: 10.1016/0040-4039(94)88062-X |
0.723 |
|
1993 |
Luzzio FA, Moore WJ. Oxidative rearrangement of sulfur-containing tertiary allylic alcohols: Synthesis of 2-cycloalkenones bearing 3-[(phenylthio)methyl] and 3-[2-alkyl-1,3-dithian-2-yl] substituents Journal of Organic Chemistry. 58: 2966-2971. DOI: 10.1021/Jo00063A011 |
0.65 |
|
1993 |
Luzzio FA, Moore WJ. Ultrasound in oxochromium(VI)-mediated transformations. 2. Ultrasound-mediated preparation and applications of chromyl chloride The Journal of Organic Chemistry. 58: 512-515. DOI: 10.1021/Jo00054A043 |
0.553 |
|
1990 |
Luzzio FA, O'Hara LC. The ultrasound-promoted aluminum amalgam reduction of phthalimides to hydroxy lactams Synthetic Communications. 20: 3223-3234. DOI: 10.1080/00397919008051550 |
0.426 |
|
1989 |
Adams LL, Luzzio FA. Ultrasound in oxochromium(VI)-amine-mediated oxidations-modifications of the Corey-Suggs oxidation for the facile conversion of alcohols to carbonyl compounds Journal of Organic Chemistry. 54: 5387-5390. DOI: 10.1021/Jo00283A041 |
0.318 |
|
1988 |
Luzzio FA, Guziec FS. Recent applications of oxochromiumamine complexes as oxidants in organic synthesis. A review Organic Preparations and Procedures International. 20: 533-584. DOI: 10.1080/00304948809356301 |
0.632 |
|
1983 |
Guziec FS, Luzzio FA. Phosphoranylidenehydrazones as in situ sources of diazo compounds: A facile synthesis of aryl-substituted benzoylcyclopropanes Journal of Organic Chemistry. 48: 2434-2437. DOI: 10.1021/Jo00162A033 |
0.704 |
|
1982 |
Guziec FS, Luzzio FA. 4-(Dimethylamino)pyridinium chlorochromate, a new selective reagent for the oxidation of allylic and benzylic alcohols Journal of Organic Chemistry. 47: 1787-1789. DOI: 10.1021/Jo00348A045 |
0.687 |
|
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