Year |
Citation |
Score |
2017 |
Lamberson CR, Muchalski H, McDuffee KB, Tallman KA, Xu L, Porter NA. Propagation Rate Constants for the Peroxidation of Sterols on the Biosynthetic Pathway to Cholesterol. Chemistry and Physics of Lipids. PMID 28174017 DOI: 10.1016/J.Chemphyslip.2017.01.006 |
0.448 |
|
2015 |
Muchalski H, Levonyak AJ, Xu L, Ingold KU, Porter NA. Competition H(D) kinetic isotope effects in the autoxidation of hydrocarbons. Journal of the American Chemical Society. 137: 94-7. PMID 25533605 DOI: 10.1021/Ja511434J |
0.462 |
|
2015 |
Muchalski H, Xu L, Porter NA. Tunneling in tocopherol-mediated peroxidation of 7-dehydrocholesterol. Organic & Biomolecular Chemistry. 13: 1249-53. PMID 25435103 DOI: 10.1039/C4Ob02377C |
0.467 |
|
2014 |
Lamberson CR, Xu L, Muchalski H, Montenegro-Burke JR, Shmanai VV, Bekish AV, McLean JA, Clarke CF, Shchepinov MS, Porter NA. Unusual kinetic isotope effects of deuterium reinforced polyunsaturated fatty acids in tocopherol-mediated free radical chain oxidations. Journal of the American Chemical Society. 136: 838-41. PMID 24380377 DOI: 10.1021/Ja410569G |
0.573 |
|
2013 |
Lamberson CR, Xu L, Muchalski H, Shchepinov MS, Porter Na. 340 – Unusual Kinetic Isotope Effects of Deuterium Reinforced Polyunsaturated Fatty Acids in Tocopherol-Mediated Free Radical Chain Oxidations Free Radical Biology and Medicine. 65. DOI: 10.1016/J.Freeradbiomed.2013.10.613 |
0.569 |
|
2012 |
Giurg M, Muchalski H, Kowal E. Oxofunctionalized trans-2-carboxycinnamic acids by catalytic domino oxidation of naphthols and hydronaphthoquinones Synthetic Communications. 42: 2526-2539. DOI: 10.1080/00397911.2011.561945 |
0.475 |
|
2011 |
Muchalski H, Doody AB, Troyer TL, Johnston JN. PREPARATION OF ISOPROPYL 2-DIAZOACETYL(PHENYL)CARBAMATE. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 88: 212-223. PMID 23180897 DOI: 10.1002/0471264229.Os088.21 |
0.727 |
|
2011 |
Troyer TL, Muchalski H, Hong KB, Johnston JN. Origins of selectivity in Brønsted acid-promoted diazoalkane-azomethine reactions (the aza-Darzens aziridine synthesis). Organic Letters. 13: 1790-2. PMID 21366339 DOI: 10.1021/Ol200313M |
0.718 |
|
2010 |
Muchalski H, Hong KB, Johnston JN. Brønsted acid-promoted azide-olefin [3 + 2] cycloadditions for the preparation of contiguous aminopolyols: The importance of disiloxane ring size to a diastereoselective, bidirectional approach to zwittermicin A. Beilstein Journal of Organic Chemistry. 6: 1206-10. PMID 21283562 DOI: 10.3762/Bjoc.6.138 |
0.739 |
|
2010 |
Johnston JN, Muchalski H, Troyer TL. To protonate or alkylate? Stereoselective Brønsted acid catalysis of C-C bond formation using diazoalkanes. Angewandte Chemie (International Ed. in English). 49: 2290-8. PMID 20209537 DOI: 10.1002/Anie.200904828 |
0.741 |
|
2010 |
Troyer TL, Muchalski H, Johnston JN. ChemInform Abstract: Broensted Acid Activation of α-Diazo Imide: A syn-Selective Glycolate Mannich Reaction. Cheminform. 41. DOI: 10.1002/chin.201010028 |
0.744 |
|
2010 |
Johnston J, Muchalski H, Troyer T. Protonierung oder Alkylierung? Stereoselektive Brønsted-Säure-katalysierte C-C-Verknüpfungen mit Diazoalkanen Angewandte Chemie. 122: 2340-2349. DOI: 10.1002/Ange.200904828 |
0.67 |
|
2009 |
Troyer TL, Muchalski H, Johnston JN. Brønsted acid activation of alpha-diazo imide: a syn-selective glycolate Mannich reaction. Chemical Communications (Cambridge, England). 6195-7. PMID 19826666 DOI: 10.1039/B913785H |
0.728 |
|
2009 |
Giurg M, Kowal E, Muchalski H, Syper L, Młochowski J. Catalytic oxidative domino degradation of alkyl phenols towards 2- and 3-substituted muconolactones Synthetic Communications. 39: 251-266. DOI: 10.1080/00397910802369687 |
0.379 |
|
2008 |
Niswender CM, Lebois EP, Luo Q, Kim K, Muchalski H, Yin H, Conn PJ, Lindsley CW. Positive allosteric modulators of the metabotropic glutamate receptor subtype 4 (mGluR4): Part I. Discovery of pyrazolo[3,4-d]pyrimidines as novel mGluR4 positive allosteric modulators. Bioorganic & Medicinal Chemistry Letters. 18: 5626-30. PMID 18793851 DOI: 10.1016/J.Bmcl.2008.08.087 |
0.447 |
|
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