Download presentation
Presentation is loading. Please wait.
Published byGwendolyn Carroll Modified over 8 years ago
1
2016-3-181 2010.05.22 刘媛媛
2
2016-3-182
3
3 University of Toronto Professor NSERC/Merck-Frosst Industrial Research Chair AstraZeneca Professor of Organic Chemistry Department of Chemistry Davenport Chemical Laboratories 80 St. George St. University of Toronto Toronto, Ontario M5S 3H6
4
2016-3-184 Personal Place and Date of BirthHamilton, Ontario, CanadaJuly 9, 1959 Education Harvard UniversityNSERC PDF with D. A. Evans1985 - 1987 University of Wisconsin-MadisonPh.D. with B. M. Trost1985 University of GuelphB.Sc. - Distinction1981 Academic Positions NSERC/Merck Frosst Industrial Research ChairNSERC/Merck Frosst2003 - present AstraZeneca Professor of Organic SynthesisUniversity of Toronto1998 - present ProfessorUniversity of Toronto1995 - 1998 Associate ProfessorUniversity of Toronto1992 - 1995 Assistant ProfessorUniversity of Toronto1987 - 1992
5
2016-3-185 Awards & Honors Senior Scientist Award Alexander von Humboldt Foundation Berlin, Aachen and Gottingen 2009-2014 Visiting ProfessorUniversity of Berlin2009 Visiting ProfessorUniversité de Marseilles2008 ICIQ Summer SchoolICIQ Tarragona, Spain2008 Attilio Corbella Summer School ProfessorItalian Chemical Society2007 Arthur C. Cope Scholar AwardAmerican Chemical Society2006 Alfred Bader AwardCanadian Society for Chemistry2006 R. U. Lemieux AwardCanadian Society for Chemistry2004 Solvias PrizeSolvias AG2002 Fellow of the Royal Society of CanadaRoyal Society of Canada2001
6
2016-3-186 The Lautens group is focused on the investigation and development of novel transition-metal-mediated organic transformations. Some projects include catalyst-controlled asymmetric transformations while others focus on controlled tandem or domino processes. Of particular interest are reactions which can efficiently construct frameworks of pharmaceutical compounds or fragments of biologically-active natural products.
7
2016-3-187
8
8 Palladium-Catalyzed Domino Reactions with C-H Bonds: Synthesis of Substituted Carbocycles and Heterocycles using Strained Alkene Shuttles
9
2016-3-189 Palladium-Catalyzed Domino Reactions with C-H Bonds: Synthesis of Substituted Carbocycles and Heterocycles using Strained Alkene Shuttles
10
2016-3-1810
11
2016-3-1811 The tandem process displays high versatility: Suzuki, Heck, and Sonogashira couplings, as well as direct arylation can be used orthogonally to carbon-nitrogen bond formation under palladium-catalyzed conditions to create a diverse set of 2- substituted indoles, and a wide range of functionality is tolerated at all positions of the benzenoid ring.
12
2016-3-1812
13
2016-3-1813
14
2016-3-1814
15
2016-3-1815
16
2016-3-1816
17
2016-3-1817
18
2016-3-1818
19
2016-3-1819
20
2016-3-1820
21
2016-3-1821
22
2016-3-1822
23
2016-3-1823
24
2016-3-1824
25
2016-3-1825
26
2016-3-1826
27
2016-3-1827
28
2016-3-1828
29
2016-3-1829
30
2016-3-1830
31
2016-3-1831
32
2016-3-1832
33
2016-3-1833
34
2016-3-1834
35
2016-3-1835
36
2016-3-1836
37
2016-3-1837
38
2016-3-1838
39
2016-3-1839
40
2016-3-1840
41
2016-3-1841
42
2016-3-1842
43
2016-3-1843
44
2016-3-1844
45
2016-3-1845
46
2016-3-1846
47
2016-3-1847
48
2016-3-1848
49
2016-3-1849
50
2016-3-1850
51
2016-3-1851
52
2016-3-1852
53
2016-3-1853
54
2016-3-1854
55
2016-3-1855
56
2016-3-1856
57
2016-3-1857
58
2016-3-1858
59
2016-3-1859
60
2016-3-1860
61
2016-3-1861
62
2016-3-1862
63
2016-3-1863
64
2016-3-1864
65
2016-3-1865
66
2016-3-1866
67
2016-3-1867
68
2016-3-1868
69
2016-3-1869
70
2016-3-1870
Similar presentations
© 2024 SlidePlayer.com Inc.
All rights reserved.