Marsha R. Baar

Microwave-Enhanced Organic Syntheses for the Undergraduate Laboratory: Diels−Alder Cycloaddition, Wittig Reaction, and Williamson Ether Synthesis

Marsha R. Baar, Danielle Falcone, Christopher P. Gordon · Journal of Chemical Education · 2009 · 24 citations

Diels−alder Cycloaddition, Chemical Engineering, Engineering +10

Interception of [2+2] cycloadducts in the zinc bromide mediated reaction of di-tert-butyl methylenemalonate with simple enol ethers

Marsha R. Baar, Paloma Ballesteros, Bryan W. Roberts · Tetrahedron Letters · 1986 · 21 citations

Cross-coupling Reaction, Engineering, Heterocyclic +7

Pedagogical Comparison of Five Reactions Performed under Microwave Heating in Multi-Mode versus Mono-Mode Ovens: Diels–Alder Cycloaddition, Wittig Salt Formation, E2 Dehydrohalogenation To Form an Alkyne, Williamson Ether Synthesis, and Fischer Esterification

Marsha R. Baar, William Gammerdinger, Jennifer Leap et al. · Journal of Chemical Education · 2014 · 17 citations

Chemical Engineering, Fischer Esterification, Engineering +14

Enantiomeric Resolution of (±)-Mandelic Acid by (1R,2S)-(–)-Ephedrine. An Organic Chemistry Laboratory Experiment Illustrating Stereoisomerism

Marsha R. Baar, Andrea L. Cerrone-Szakal · Journal of Chemical Education · 2005 · 15 citations

Research Experience for the Organic Chemistry Laboratory: A Student-Centered Optimization of a Microwave-Enhanced Williamson Ether Synthesis and GC Analysis

Marsha R. Baar · Journal of Chemical Education · 2018 · 12 citations

Inquiry-based Experiment, Chemical Engineering, Chemical Measurement +14