Yahoo Suche Web Suche

Suchergebnisse

  1. Suchergebnisse:
  1. School of Pharmaceutical Science and Technology, Tianjin University, Tianjin, China Jay S. Siegel Department of Chemistry, National Cheng Kung University, Tainan, Taiwan Yao-Ting Wu Bibliographic Information. Book Title: Polyarenes I. Editors: Jay S. Sie ...

  2. Jay Siegel, dean of the Health Science Platform at Tianjin University, points out that traditional Chinese medicine also depends on complex inputs and, therefore, can benefit from big data analysis. "TCM looks at the whole system, as opposed to Western medicine, which is more reductionist and focuses on one or a few effective elements," he says.

  3. Prof Jay S. Siegel School of Pharmaceutical Science and Technology Tianjin University (A203/Bldg 24) 92 Weijin Road, Nankai District Tianjin, 300072 PRC. Tel +86-22-87402050 e-mail dean_spst@tju.edu.cn. Jay S. Siegel received his Ph. D. from Princeton working with Kurt Mislow. He was a Swiss Universities Fellow at ETH Zurich, with Professor ...

  4. Professor Siegel is a specialist in the area of molecular design and synthesis, with a focus on physical organic chemistry and the stereochemistry of aromatic and supramolecular architectures. His work impacts core concepts of stereochemistry, including biological homochirality and its implications in the origin of life. He has also been a pioneer in the field of non-planar aromatic materials ...

  5. 29. Aug. 2018 · Renowned scholar Jay Siegel said he expects China's efforts to encourage innovation and creativity among students will propel the country's science education to new heights. Siegel, 59, has been at the forefront of extensive reforms at Tianjin University since joining its School of Pharmaceutical Science in 2011.

  6. 17. Nov. 2016 · Jay Siegel, Tianjin University. “I was struck by the enthusiasm and the desire to grow,” Chiribella told the South China Morning Post. “It was a feeling that people value you and need you ...

  7. 26. März 2018 · Annulated corannulenes 3–5 form via distinct synthetic pathways: (i) Pd-catalyzed sp3 CH insertion, (ii) Pd-catalyzed aryl coupling, and (iii) silyl cation-promoted C–F activation/CH insertion. Crystal structure, redox, and photophysical studies elucidate the differing influence of 1,2,3- versus 1,2-indeno ring fusions. Mono and dianions of 3–5 are characterized. Resolution of 4 gives ...