Problem Set – Litterature

Slides:

Advertisements

Similar presentations

For(int i = 1; i

Advertisements

1 Sébastien Goudreau Literature meeting : Rhodium(I) Chemistry Rhodium(I)

Asymmetric Total Synthesis of Nakadomarin A Li Nan

Amphidinolide A Isolation: 1. Kobayashi, J. et al. Tetrahedron Lett. 1986, 27, Kobayashi, J. et al. J. Nat. Prod. 1991, 54, Biological Activity:

CDC Reaction Involving α -C-H Bonds of Nitrogen in Amines 李南

1 Chiral Anion-Mediated Asymmetric Ion Pairing Chemistry Reporter: Zhi-Yong Han

Pierre-André Fournier

Tobe Lab Ayumi Yoshizaki

Iron Catalyzed Cross-Coupling Reaction: Recent Advances and Primary Mechanism Wang Chao

Rhodium Catalyzed Direct C-H Functionalization 陈殿峰

Catalytic Cross-coupling Reactions with Unactivated Alkyl Electrophiles and Alkyl Nucleophiles Heng Su 04/11/2008 Department of Chemistry Brandeis University.

Reporter: Yu Ting Huang Advising Prof: Ru Jong Jeng 1.

Recent Development for Stereoselective Synthesis of 1,3-Polyol Ye Zhu Prof. Burgess’ Group Aug. 19, 2010.

(-)-Kendomycin Angew. Chem. Int. Ed. 2009,48,()

Enantioselective Total Synthesis of Ecteinascidin 743

A Cyclopropane Fragmentation Approach to Heterocycle Assembly Kevin Minbiole James Madison University August 11, 2005.

Quick Reference to Pericyclic Reactions and Photochemistry Claude Legault Litterature Meeting December 13 th, 2004.

1 Rh-Catalyzed Asymmetric Additions: The Rise of Chiral Dienes Daniela Sustac February 16, 2010 Tamio HayashiErick Carreira.

Promising molecules in Drug Discovery : Syntheses and Applications of Oxetanes. A presentation by Guillaume Pelletier on October 6 th 2009.

1. 2 What is Click Chemistry? Reactions with the following characteristics: Modular, wide in scope Afford high yields w/o purification Stereospecific.

Total Synthesis of ( ‒ )-Colombiasin A and ( ‒ )-Elisapterosin B by two different approaches A presentation by Guillaume Pelletier April 27 th 2012.

Recent Progress in sp 3 C-H Activation Catalyzed by Palladium Bo Yao.

化学系 Department of Chemistry Catellani Reaction

The Career of Chao-Jun Li Guochang B.S. Zhengzhou University 1979 M.S. Chinese Academy of Science 1985 Tak-Hang ChanTak-Hang Chan Ph.D. McGill.

Buchwald-Hartwig Cross Coupling Reaction Reporter: Ying-Chieh CHAO Lecturer: Professor Guey-Sheng Liou Advisor: Professor Ru-Jong Jeng Data:2013/12/27.

Catalytic Enantioselective Allylic Amination of Unactivated Terminal Olefins Via an Ene Reaction / [2,3]-Rearrangement Hongli Bao & Uttam K. Tambar Guillaume.

Metal-Mediated Ring Formation The contribution of Paul A. Wender Guillaume Barbe Charette’s Laboratories Université de Montréal October 30 th 2007.

Advances in Metal Mediated Intramolecular Enyne Carbocyclizations Patrick D. Pohlhaus The University of North Carolina at Chapel Hill March 28, 2003.

Total Synthesis of Communesins Jian-Zhou Huang

Synthesis of meso-substituted porphyrins

Mingli Li ( stored as THF solutions, blue-green for SmI 2 and yellow-green for YbI 2 ) Deoxygenation Reactions Reductions of Double Bonds.

Reactions Involve Sulfur Ylides 陈殿峰陈殿峰

Asymmetric BINOL-Phosphate Derived Brønsted Acids: Development and Catalytic Mechanism Reporter: Song Feifei Supervisor: Prof. Yong Huang

Organic Pedagogical Electronic Network Properties of Hydrogen Bonding Created by Max Taggart Edited by Margaret Hilton Honors Organic Chemistry Chem 2321.

Regioselective reactions of 3,4-pyridynes enabled

Jean-Louis Brochu Department of Chemistry University of Ottawa

The Work Of Pr Karl A. Scheidt Group Department of Chemistry, Northwestern UniVersity, Evanston.

Redox Neutral Reactions Wang Chao Redox Economy and Redox Neutral Reactions: Angew. Chem. Int. Ed. 2009, 48, 2854 – 2867.

Organic Pedagogical Electronic Network An Introduction to Catalytic Nitrene C–H Oxidation Ashley M. Adams, Justin Su, And J. Du Bois.

Synthesis of novel polycyclic aromatic hydrocarbons by transannular cyclization Tobe Laboratory M1 Yamane Hiroshi.

Recycling the Waste: The Development of a Catalytic Wittig Reaction Angew. Chem. Int. Ed. 2009, 48, 6836 –6839.

Total synthesis of Piperazic acid-containing natural products: Piperazimycin A and Chloptosin Liu Bin

Reporter: Yang Chao Supervisor: Prof. Yong Huang The Transformation of α ‑ Diazocarbonyl Compounds.

C-H Insertion Story Justin Du Bois associate professor : University of Stanford B.S. : University of California at Berkeley (1992) Ph.D. : California Institute.

Reporter: Qinglan Liu Supervisor: Prof. Yong Huang

Nicolas Gaeng Group seminar – LSPN – 30/04/15. Structures with multiple rings connected through one atom Nomenclature proposed by Adolf Baeyer in 1900.

Enantioselective Reactions Catalyzed by Iron Complexes Pablo Pérez.

Cinchona Alkaloids : Efficient Bifunctional Organocatalyts in Asymmetric Synthesis Antonin Clemenceau Frontiers in Chemical Synthesis PhD in J. Zhu Group.

Palladium-catalysed reactions involving isocyanides Reporter: Xinzheng Chen Supervisor: Prof. David Zhigang Wang

Nitrogen–Carbon Bond Formation from N 2 and CO 2 Promoted by a Hafnocene Dinitrogen Complex Yields a Substituted Hydrazine Wesley H. Bernskoetter, Emil.

Synthesis of Daphnilongeranine C

Visible light photoredox-controlled reactions of N-radicals

Presented by Guillaume Pelletier. March 11th 2008.

Total Synthesis of (±)-Cylindricine C

Superbisor: Yong Huang

Wavelength Tunability

Enantioselective Total Synthesis of (+)-Gelsemine

Michael J. Krische Presented by Louis-Philippe Beaulieu

C-H Insertion of Rhodium-Carbene Using Diazo Compounds

Dodecahedrane Paquette, L. A. Chem. Rev. 1989, 89, 1051–1065.

Total Synthesis of (±)-Indolizomycin

Copper Catalyzed C-N Bond Formation Using O-Acyl Hydroxylamine

Hydrozirconation/Transmetalation with Zinc

Total Synthesis of Epothilone A: The Olefin Metathesis Approach

Angew. Chem. Int. Ed., 2010, 49, Early View

Principles of Organic Synthesis in Pure Water

1. Palladium Catalyzed Organic Transformations

Diels-Alder in Aqueous Molecular Hosts:

Presentation transcript:

Problem Set – Litterature A presentation by Guillaume Pelletier on October 27th 2009

Question #1: [1,4]-Conjugated Addition of an Organo-Rhodium speicies. (a) Wuitschik, G.; Rogers-Evans, M.; Müller, K.; Fisher, H.; Wagner, B.; Schuler, F.; Polonchuk, L.; Carreira, E. M. Angew. Chem. Int. Ed. 2006, 45, 7736-7739. (b) Fagnou, K.; Lautens, M. Chem. Rev. 2003, 103, 169-193.

Question #1: [1,4]-Conjugated Addition of an Organo-Rhodium speicies. (a) Wuitschik, G.; Rogers-Evans, M.; Müller, K.; Fisher, H.; Wagner, B.; Schuler, F.; Polonchuk, L.; Carreira, E. M. Angew. Chem. Int. Ed. 2006, 45, 7736-7739. (b) Fagnou, K.; Lautens, M. Chem. Rev. 2003, 103, 169-193.

Question #2: Formation of an [1,2]-trans-Aminoalcohol from an Oxetane. Bach, T.; Schröder, J. J. Org. Chem. 1999, 64, 1265-1273.

Question #2: Formation of an [1,2]-trans-Aminoalcohol from an Oxetane. Bach, T.; Schröder, J. J. Org. Chem. 1999, 64, 1265-1273.

Question #3: Oxetane by fragmentation (a) Marshall, J. A.; Arrington, J. P. J. Org. Chem. 1971, 36, 214-215. (b) Waters, J. A.; Witkop, B. J. Org. Chem. J. Org. Chem. 1969, 34, 3774.

Question #3: Oxetane by fragmentation Marshall, J. A.; Arrington, J. P. J. Org. Chem. 1971, 36, 214-215. (b) Waters, J. A.; Witkop, B. J. Org. Chem. J. Org. Chem. 1969, 34, 3774. (c) Moran, J.; Dornan, P.; Beauchemin, A. M. Org. Lett. 2007, 9, 3893-3896.

Question #3: Oxetane by fragmentation Marshall, J. A.; Arrington, J. P. J. Org. Chem. 1971, 36, 214-215. (b) Waters, J. A.; Witkop, B. J. Org. Chem. J. Org. Chem. 1969, 34, 3774. (c) Moran, J.; Dornan, P.; Beauchemin, A. M. Org. Lett. 2007, 9, 3893-3896.

Question #3: Oxetane by fragmentation Marshall, J. A.; Arrington, J. P. J. Org. Chem. 1971, 36, 214-215. (b) Waters, J. A.; Witkop, B. J. Org. Chem. J. Org. Chem. 1969, 34, 3774. (c) Moran, J.; Dornan, P.; Beauchemin, A. M. Org. Lett. 2007, 9, 3893-3896.

Question #4: Allylic strain Bach, T.; Jödicke, K.; Kather, K.; Frölich, R. J. Am. Chem. Soc. 1997, 119, 2437-2445.

Question #4: Allylic strain Bach, T.; Jödicke, K.; Kather, K.; Frölich, R. J. Am. Chem. Soc. 1997, 119, 2437-2445.

Question #5 : « Norrish type 2-like » fragmentation Booker-Milburn, K. I.; Baker, J. R.; Bruce, I. Org. Lett. 2004, 6, 1481-1484.

Question #5 : « Norrish type 2-like » fragmentation Booker-Milburn, K. I.; Baker, J. R.; Bruce, I. Org. Lett. 2004, 6, 1481-1484.