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Martin D. Burke
Martin D. Burke
Professor of Chemistry, University of Illinois and Associate Dean for Research, CIMED
Verified email at illinois.edu - Homepage
Title
Cited by
Cited by
Year
A Planning Strategy for Diversity-Oriented Synthesis
MD Burke, SL Schreiber
Angewandte Chemie - International Edition 43 (1), 46-58, 2004
17852004
Amphotericin primarily kills yeast by simply binding ergosterol
KC Gray, DS Palacios, I Dailey, MM Endo, BE Uno, BC Wilcock, MD Burke
Proceedings of the National Academy of Sciences 109 (7), 2234-2239, 2012
6962012
A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates
DM Knapp, EP Gillis, MD Burke
Journal of the American Chemical Society 131 (20), 6961-6963, 2009
6722009
A simple and modular strategy for small molecule synthesis: iterative Suzuki− Miyaura coupling of B-protected haloboronic acid building blocks
EP Gillis, MD Burke
Journal of the American Chemical Society 129 (21), 6716-6717, 2007
5702007
Synthesis of many different types of organic small molecules using one automated process
J Li, SG Ballmer, EP Gillis, S Fujii, MJ Schmidt, AME Palazzolo, ...
Science 347 (6227), 1221-1226, 2015
5392015
Amphotericin forms an extramembranous and fungicidal sterol sponge
TM Anderson, MC Clay, AG Cioffi, KA Diaz, GS Hisao, MD Tuttle, ...
Nature chemical biology 10 (5), 400-406, 2014
4902014
Generating diverse skeletons of small molecules combinatorially
MD Burke, EM Berger, SL Schreiber
Science 302 (5645), 613-618, 2003
4532003
Simple, efficient, and modular syntheses of polyene natural products via iterative cross-coupling
SJ Lee, KC Gray, JS Paek, MD Burke
Journal of the American Chemical Society 130 (2), 466-468, 2008
3422008
Multistep synthesis of complex boronic acids from simple MIDA boronates
EP Gillis, MD Burke
Journal of the American Chemical Society 130 (43), 14084-14085, 2008
2822008
A general solution for the 2-pyridyl problem
GR Dick, EM Woerly, MD Burke
Angewandte Chemie (International ed. in English) 51 (11), 2667, 2012
2492012
Eine Strategie für die Diversitäts‐orientierte Synthese
MD Burke, SL Schreiber
Angewandte Chemie 116 (1), 48-60, 2004
2462004
Iterative cross-couplng with MIDA boronates: towards a general platform for small molecule synthesis
EP Gillis, MD Burke
Aldrichimica acta 42 (1), 17, 2009
2452009
Synthesis of most polyene natural product motifs using just 12 building blocks and one coupling reaction
EM Woerly, J Roy, MD Burke
Nature chemistry 6 (6), 484-491, 2014
2202014
A synthesis strategy yielding skeletally diverse small molecules combinatorially
MD Burke, EM Berger, SL Schreiber
Journal of the American Chemical Society 126 (43), 14095-14104, 2004
2152004
Synthesis-enabled functional group deletions reveal key underpinnings of amphotericin B ion channel and antifungal activities
DS Palacios, I Dailey, DM Siebert, BC Wilcock, MD Burke
Proceedings of the National Academy of Sciences 108 (17), 6733-6738, 2011
1852011
From Synthesis to Function via Iterative Assembly of N-Methyliminodiacetic Acid Boronate Building Blocks
J Li, AS Grillo, MD Burke
Accounts of chemical research 48 (8), 2297-2307, 2015
1842015
The Molecular Industrial Revolution: Automated Synthesis of Small Molecules
M Trobe, MD Burke
Angewandte Chemie International Edition 57 (16), 4192-4214, 2018
1812018
Pinene-Derived Iminodiacetic Acid (PIDA): A Powerful Ligand for Stereoselective Synthesis and Iterative Cross-Coupling of C(sp3) Boronate Building Blocks
J Li, MD Burke
Journal of the American Chemical Society 133 (35), 13774-13777, 2011
1712011
Vinyl MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis
BE Uno, EP Gillis, MD Burke
Tetrahedron 65 (16), 3130-3138, 2009
1682009
Stereoretentive Suzuki− Miyaura Coupling of Haloallenes Enables Fully Stereocontrolled Access to (−)-Peridinin
EM Woerly, AH Cherney, EK Davis, MD Burke
Journal of the American Chemical Society 132 (20), 6941-6943, 2010
1542010
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