Dramatic rate accelerations of Diels-Alder reactions in 5 M lithium perchlorate-diethyl ether: the cantharidin problem reexamined

PA Grieco, JJ Nunes, MD Gaul - Journal of the American Chemical …, 1990 - ACS Publications
During the past 15 years, studies on the Diels-Alder reaction1 have produced dramatic results.
The pronounced rate enhancements and improved stereoselectivities observed to date …

Fmoc mediated synthesis of peptide nucleic acids

SA Thomson, JA Josey, R Cadilla, MD Gaul… - Tetrahedron, 1995 - Elsevier
The syntheses of the Fmoc-protected Peptide Nucleic Acid (PNA) monomer pentafluorophenyl
esters of adenine (26), cytosine (23), guanine (29) and thymine (20), and their …

Identification of diaryl ether-based ligands for estrogen-related receptor α as potential antidiabetic agents

…, JM Lenhard, MR Player, MD Gaul - Journal of medicinal …, 2011 - ACS Publications
Estrogen-related receptor α (ERRα) is an orphan nuclear receptor that has been functionally
implicated in the regulation of energy homeostasis. Herein is described the development of …

[HTML][HTML] The use of stable isotope-labeled glycerol and oleic acid to differentiate the hepatic functions of DGAT1 and-2

…, GW Caldwell, MJ Todd, Y Liang, MD Gaul… - Journal of lipid …, 2012 - ASBMB
Diacylglycerol acyltransferase (DGAT) catalyzes the final step in triglyceride (TG) synthesis.
There are two isoforms, DGAT1 and DGAT2, with distinct protein sequences and potentially …

Indazole-based ligands for estrogen-related receptor α as potential anti-diabetic agents

…, HB Askari, J Liu, J Kasturi, M Towers, MD Gaul… - European journal of …, 2017 - Elsevier
Estrogen-related receptor α (ERRα) is an orphan nuclear receptor that has been functionally
implicated in the regulation of energy homeostasis. Herein is described the development of …

Enantioselective ring construction: synthesis of (+)-estrone methyl ether

DF Taber, K Raman, MD Gaul - The Journal of Organic Chemistry, 1987 - ACS Publications
The estrogenic steroids have been the target of extensive synthetic investigation, 2 both
because they are economi-cally significant and because they are among the struc-turally …

Synthesis and biological evaluation of benzocyclobutane-C-glycosides as potent and orally active SGLT1/SGLT2 dual inhibitors

GH Kuo, MD Gaul, Y Liang, JZ Xu, F Du… - Bioorganic & Medicinal …, 2018 - Elsevier
… Author links open overlay panel Gee-Hong Kuo , Micheal D. Gaul , Yin Liang , June Z. Xu ,
Fuyong Du , Pamela Hornby , Guozhang Xu , Jenson Qi , Nathaniel Wallace , Seunghun Lee , …

Enantioselective construction of dialkylcarbinols: synthesis of (-)-5-hexadecanolide

DF Taber, PB Deker, MD Gaul - Journal of the American Chemical …, 1987 - ACS Publications
Alcohol 2 is designed to block one face of the carbonyls inthe derived ß-keto ester 3. Hydride
reduction can then proceed either via the transition state in which the carbonyls are syn (…

Potent sodium/glucose cotransporter SGLT1/2 dual inhibition improves glycemic control without marked gastrointestinal adaptation or colonic microbiota changes in …

…, T Kirchner, M Jennis, W Lang, GH Kuo, MD Gaul… - … of Pharmacology and …, 2018 - ASPET
The sodium/glucose cotransporters (SGLT1 and SGLT2) transport glucose across the intestinal
brush border and kidney tubule. Dual SGLT1/2 inhibition could reduce hyperglycemia …

Discovery and biological evaluation of potent dual ErbB-2/EGFR tyrosine kinase inhibitors: 6-thiazolylquinazolines

MD Gaul, Y Guo, K Affleck, GS Cockerill… - Bioorganic & medicinal …, 2003 - Elsevier
We have identified a novel class of 6-thiazolylquinazolines as potent and selective inhibitors
of both ErbB-2 and EGFR tyrosine kinase activity, with IC 50 values in the nanomolar range. …