George J. Schroepfer
Affiliations: | Rice University, Houston, TX |
Area:
Plant Pathology Agriculture, Biochemistry, Organic ChemistryGoogle:
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Publications
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| Ruan B, Lai PS, Yeh CW, et al. (2002) Alternative pathways of sterol synthesis in yeast. Use of C(27) sterol tracers to study aberrant double-bond migrations and evaluate their relative importance. Steroids. 67: 1109-19 |
| Lindenthal B, Holleran AL, Aldaghlas TA, et al. (2001) Progestins block cholesterol synthesis to produce meiosis-activating sterols. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 15: 775-84 |
| Ruan B, Wilson WK, Pang J, et al. (2000) Synthesis of [3alpha-3H]cholesta-5,8-dien-3beta-ol and tritium-labeled forms of other sterols of potential importance in the Smith-Lemli-Optiz syndrome. Steroids. 65: 29-39 |
| Ruan B, Wilson WK, Schroepfer GJ. (1999) An improved synthesis of (20R,22R)-cholest-5-ene-3β,20,22-triol, an intermediate in steroid hormone formation and an activator of nuclear orphan receptor LXRα Steroids. 64: 385-395 |
| Li S, Pang J, Wilson WK, et al. (1999) Sterol synthesis. Preparation and characterization of fluorinated and deuterated analogs of oxygenated derivatives of cholesterol. Chemistry and Physics of Lipids. 99: 33-71 |
| Li S, Pang J, Wilson WK, et al. (1999) A new approach to the stereoselective total synthesis of isotopically labeled d-ribo-phytosphingosine Tetrahedron-Asymmetry. 10: 1697-1707 |
| Li S, Pang J, Wilson WK, et al. (1999) Efficient synthesis of deuterium‐ and tritium‐labeled d‐erythro‐sphingosine Journal of Labelled Compounds and Radiopharmaceuticals. 42: 815-826 |
| Su X, Wilson WK, Schroepfer GJ. (1999) Synthesis of deuterium- and tritium-labeled 25,26,26,26,27,27,27-heptafluorocholesterol Journal of Labelled Compounds and Radiopharmaceuticals. 42: 509-518 |
| Carroll JN, Pinkerton FD, Su X, et al. (1998) Sterol synthesis, Synthesis of 3β-hydroxy-25,26,26,26,27,27,27-heptafluorocholest-5-en-7-one and its effects on HMG-CoA reductase activity in Chinese hamster ovary cells, on ACAT activity in rat jejunal microsomes, and serum cholesterol levels in rats Chemistry and Physics of Lipids. 94: 209-225 |
| Su X, Siddiqui A, Swaminathan S, et al. (1998) Preparation of 25,26,26,26,27,27,27-heptafluoro-15-ketosterols labeled at C-23 with deuterium or tritium Journal of Labelled Compounds and Radiopharmaceuticals. 41: 63-74 |