PPT-Pyridine C–H Functionalization

Author : sherrill-nordquist | Published Date : 2016-06-25

The Sarpong Lab University of California Berkeley 2014 Ubiquity and Importance of Substituted Pyridine Derivatives Pharmaceutical Agents Bioactive Natural Products

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Pyridine C–H Functionalization: Transcript


The Sarpong Lab University of California Berkeley 2014 Ubiquity and Importance of Substituted Pyridine Derivatives Pharmaceutical Agents Bioactive Natural Products Various Approaches to Functionalize Pyridines. HOOOHOMeNRMeNMeMeR=H: TubocurarinR=Me: Wrong struct.NNEx. Mivacurium kloridMuscle relax, HOOHSuccinsyrekolinSuksametonium, Curacit properties. Nadine KARAKI. International . Conference. and Exhibition on . Biopolymers. and . Bioplastics. August 10-12,2015 San Francisco, . USA. Supervisors. : Lionel . Muniglia. , . Abdulhadi. . The Synthesis of Pyridine Derivatives using . N. -Heteroatom Pyridinium . Species. Group Seminar – 24.09.2015. Cyril Piemontesi. 1. Content. The Synthesis of Pyridine Derivatives using . N. -Heteroatom Pyridinium Species. Rings . Pyridne. , . quinoline. and . isoquinoline. Pyridne. Pyridine is a water -miscible liquid, b. p. 115 . oC. with . an unpleasant . odour. An . Excelent. polar . solvent, A . base (. NOMENCLATURE & RING SYNTHESIS. NOMENCLATURE OF HETEROCYCLIC COMPOUNDS. DEFINITION:. A cyclic organic compound containing all carbon atoms in ring formation is referred to as a carbocyclic compound.. properties. Nadine KARAKI. International . Conference. and Exhibition on . Biopolymers. and . Bioplastics. August 10-12,2015 San Francisco, . USA. Supervisors. : Lionel . Muniglia. , . Abdulhadi. . The . Sarpong. Lab. University of California, Berkeley. 2014. Ubiquity and Importance of Substituted Pyridine Derivatives. Pharmaceutical Agents:. Bioactive Natural . Products. :. Approaches . to Functionalize Pyridines. Why is:. Mn. 2+. (. aq. ) colorless. Cu. 2+. (. aq. ) less deeply blue colored than Cu(NH. 3. ). 4. 2+. Zn. 2+. (. aq. ) colorless. MnO. 4. -. deeply colored. W(CO). 6. colorless. Sigma Interaction Strength. Why is:. Mn. 2 . (. aq. ) colorless. Cu. 2 . (. aq. ) less deeply blue colored than Cu(NH. 3. ). 4. 2 . Zn. 2 . (. aq. ) colorless. MnO. 4. -. deeply colored. W(CO). 6. colorless. Sigma Interaction Strength. from NANOTECHNOLOGY capacitors batteries flexible electronics composites filtrations sensors etcGraphene is a high aspect ratio nanocarbon material x0000 50001 possibleCost-efficient volume scalable g b. ]pyridines Derivatives with Potent . Antichagasic. Activity. Júlio César Soares . 1,. *, Joana Ribeiro . 1. , Camilo Henrique Lima . 1. , Gisele Portapilla. 2. , Sérgio de Albuquerque. 2. and Luiza Dias. Asso. . Prof. . Dept of Chemistry. Properties Of Thiophene. At . room temperature, thiophene is a colorless liquid with a mildly pleasant odor reminiscent of . benzene.. It’s boiling point is 84°C and melting point -38°C.. Ahmed Aido . 1,2,. *, Harald Wajant . 2. , . Matej Buzgo. 1. . and Aiva Simaite . 1. 1. . InoCure. . s.r.o. , . R&d. Lab, . Prumyslová. 1960, 250 88 . Celákovice. , Czech Republic; aiva@inocure.cz; . Lycium. . barbarum. (goji) puree. Monica . Rosa . Loizzo. 1,*. , . Antonio . Mincione. 1. , . Rosa . Tundis. 1. , . Vincenzo . Sicari. 2. 1. Department . of . Pharmacy, . Health and . Nutritional .

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