Physical Sciences and Mathematics Commons^™

New Syntheses Of Diaryl Ethers, Tyrosinols, B-Hydroxytyrosinols, L,L-Isodityrosinol And L,L-Isodityrosine-Derived Agents Via The Diels-Alder Reaction, Xianqi Feng

All Graduate Theses and Dissertations, Spring 1920 to Summer 2023

Syntheses of diaryl ethers were approached by use of a Diels-Alder reaction employing a new type of diene attached with an aryloxy group. Thus, 2-methyl-3-phenoxybutadiene (90b ), 2- methoxy-3-phenoxybutadiene (92b) and (4S)-3-(t- butyloxycarbony1)-2 ,2-dimethyl-4-( 4-(3-methoxy-1,3 -butadienyl-2- oxy )phenylmethyl]oxazolidine (93b) were synthesized in ~65% yields by methylenation of the carbonyl function in the corresponding 2- substituted acrylate aryl ester using Tebbe's reagent. The 1,3- bis[(trimethylsilyl)oxy ]-2-phenoxybutadiene (105) was made from 1-phenoxy-2-propanone (101) by a sequence of formylation and enolsilylation. Methyl propiolate (107) and dimethyl acetylenedicarboxylate (113) were heated at reflux with diene 9 0 b and 92b in toluene to provide …

The Reaction Of Dimethyl-And Di-N-Butylcopper Lithium With 3-Bromo-2-(2-Phenylacetamido) Acrylic Acid, Kim David Richards

All Graduate Theses and Dissertations, Spring 1920 to Summer 2023

The reaction of dimethylcopper lithium and di-n-butylcopper lithium with 3-bromo-2-(2-phenylacetamido) acrylic acid, mp 174 - 175°, produced as major products 3-methyl-2-(2-phenylacetamido) acrylic acid and 3-n-butyl-2-(2-phenylacetamido) acrylic acid, respectively. The dimethylcopper lithium reaction was stereospecific for the E geometrical isomer, mp 198 - 199°, and produced 3-methyl-2-(2-phenylacetamido) acrylic acid and 2-(2-phenylacetamido) acrylic acid in a 3:1 molar ratio, respectively. The di-n-butylcopper lithium reaction produced as the main products 3-n-butyl-2-(2-phenylacetamido) acrylic acid and 2-(2- phenylacetamido) acrylic acid in a 7:1 molar ratio, respectively, with the 3-n-butylacrylic acid comprising 83% of the product. The reaction …

The Reaction Of Some Sodium Salts Of Fatty Acids And Benzoic Acid With Α-Bromobenzyl Cyanide, Richard W. Perkins

All Graduate Theses and Dissertations, Spring 1920 to Summer 2023

Fife (4) and O'Shaughnessy (12) have made a series of di-esters by allowing the sodium salts of various fatty acids to react with ethyl monochloracetate according to the following equation:

RCO₂Na ≠ ClCH₂CO₂C₂H₅ ---------> RCO₂CH₂CO₂C₂H₅ ≠ NaCl .

The mechanism of the reaction appears to be ionic and to involve the attack of an RCO₂^- ion on the carbon atom to which the chlorine atom is attached. As the RCO₂^- approaches this carbon atom the chlorine atom moves …