E. Tabet

发表

Asymmetric Aldol Additions with Titanium Enolates of Acyloxazolidinethiones: Dependence of Selectivity on Amine Base and Lewis Acid Stoichiometry

B. W. King, M. Crimmins, E. Tabet, 1997 .

Asymmetric aldol additions: use of titanium tetrachloride and (-)-sparteine for the soft enolization of N-acyl oxazolidinones, oxazolidinethiones, and thiazolidinethiones.

B. W. King, M. Crimmins, E. Tabet, 2001, The Journal of organic chemistry.

Selective Continuous Flow Iodination Guided by Direct Spectroscopic Observation of Equilibrating Aryl Lithium Regioisomers

Anna L. Dunn, Bernie O’Hare, P. Liu, 2018, Organometallics.

Formal total synthesis of (+)-trehazolin. Application of an asymmetric aldol-olefin metathesis approach to the synthesis of functionalized cyclopentenes.

M. Crimmins, E. Tabet, 2001, The Journal of organic chemistry.

A Scaleable Synthesis of Methyl 3-Amino-5-(4-fluorobenzyl)-2-pyridinecarboxylate

S. A. Burova, M. Sharp, C. Koble, 2007 .

Ir C–H Activation and Other Catalysis Applied to a Complex Drug Candidate

Bing Liu, Roman. Davis, V. Elitzin, 2012, Topics in Catalysis.

CYCLIC VOLTAMMETRY WITH ULTRAMICROELECTRODES

R. Dudek, E. Tabet, S. Ching, 1994 .

Synthesis of 7-trifluoromethylpyrazolo[1,5-a]pyridinedicarboxylate

Roman. Davis, V. Elitzin, E. Tabet, 2012 .

Asymmetric aldol additions: use of titanium tetrachloride and (-)-sparteine for the soft enolization of N-acyl oxazolidinones, oxazolidinethiones, and thiazolidinethiones.

B. W. King, M. Crimmins, E. Tabet, 2001, The Journal of organic chemistry.

Development of a New Synthesis for the Large-Scale Preparation of Triple Reuptake Inhibitor (−)-GSK1360707

M. Sharp, V. Elitzin, E. Tabet, 2010 .

An aldol approach to the synthesis of the EF fragment of spongistatin 1.

M. Crimmins, S. Kirincich, J. Katz, 2001, Organic letters.

Effects of nitrogen and alkene substitution on the PtCl2 catalyzed cycloisomerization of N-tethered 1,6-enyne precursors to the triple reuptake inhibitor GSK1360707

M. Sharp, V. Elitzin, E. Tabet, 2011 .

Solvent-Free Friedel–Crafts Cyclization with Trichloroacetic Anhydride

Roman. Davis, E. Tabet, Andrew J. Hazelwood, 2009 .

Total Synthesis of (+)-Prelaureatin and (+)-Laurallene

M. Crimmins, E. Tabet, 2000 .

Correlation of F0F1-ATPase inhibition and antiproliferative activity of apoptolidin analogues.

H. Seto, P. Wender, Kate E. Longcore, 2006, Organic letters.

Facile synthetic access to and biological evaluation of the macrocyclic core of apoptolidin.

H. Seto, P. Wender, E. Tabet, 2003, Organic letters.

Toward a structure-activity relationship for apoptolidin: selective functionalization of the hydroxyl group array.

H. Seto, P. Wender, E. Tabet, 2003, Organic letters.

Synthesis of 4‐Substituted Piperidines via a Mild and Scalable Two‐Step Cu2O‐Mediated Decarboxylation of Cyanoesters

W. Kazmierski, B. Chauder, C. Koble, 2006 .

Synthesis of 4-Substituted Piperidines via a Mild and Scalable Two-Step Cu2O-Mediated Decarboxylation of Cyanoesters.

W. Kazmierski, B. Chauder, C. Koble, 2006 .

An enyne cycloisomerization approach to the triple reuptake inhibitor GSK1360707F.

N. Deschamps, M. Sharp, M. Mitchell, 2011, The Journal of organic chemistry.

A FORMAL PCB-FREE SYNTHESIS OF (-)-GSK1360707 VIA A DOUBLE ALKYLATION REACTION (Dedicated to Professor Victor Snieckus on the occasion of his 77th birthday)

M. Sharp, V. Elitzin, E. Tabet, 2014 .