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 Forschungsbericht für das Jahr 2017

Institut für Organische Chemie

Arbeitskreis Prof. Dr. Reinhard Brückner

Albertstr. 21
79104 Freiburg
Tel: 0049-(0)761-203-6029 Fax: 0049-(0)761-203-6100
Email reinhard.brueckner@organik.chemie.uni-freiburg.de
http://www.chemie.uni-freiburg.de/orgbio/brueck/w3br/


Einträge in der Rubrik "Who is Who"

Wissenschaftliche Publikationen

Originalarbeiten in wissenschaftlichen Fachzeitschriften:
  • Arican D, Braukmüller S, Brückner R: Regioselective Bromination of Benzocycloheptadienones for the Synthesis of Substituted 3,4-Benzotropolones Including Goupiolone A Chem-eur J, 2017; 23: 4537-4541.
  • Diehl J, Brückner R: Synthesis of Enantiomerically Pure β-Hydroxyketones via β-Keto Weinreb Amides by a Condensation / Asymmetric Hydrogenation / Acylation Sequence Eur J Org Chem, 2017; 2017: 278-286.
  • Engesser T, Brückner R: Synthesis of trans-Configured Enol Ethers by a Sequence of syn-Selective Glycolate Aldol Addition, Hydrolysis, and Grob Fragmentation Eur J Org Chem, 2017; 2017: 5789-5794.
  • Hampel T, Brückner R: Towards a Total Synthesis of Phenalinolactone Core Diterpenoid 6: Synthesis of a Racemic Decahydrobenzocyclobutaisobenzofuran With a trans-anti-cis Junc¬tion of the Isocyclic Rings Eur J Org Chem, 2017; 2017: 2950-2963.
  • Hermann D, Arican D, Brückner R: Two-Step Synthesis of (Z)-3-Aryl-5-(arylmethylidene)butenolides by an Ivanov Reaction / Ag(I)-Catalyzed Lactonization / in-situ Dehydration Sequence Synthesis-stuttgart, 2017; 49: 326-352.
  • Neumeyer M, Brückner R: Die erste stereoselektive Totalsynthese eines dimeren γ-Lactonanellierten Py¬rano¬naph¬tho¬chi¬nons: γ-Actinorhodin Angewandte Chemie, 2017; 128: 3432-3437.
  • Neumeyer M, Brückner R: First Stereoselective Total Synthesis of a Dimeric Naphthoquinonopyrano-γ-lactone: γ-Actinorhodin Angew Chem Int Edit, 2017; 56: 3383-3388.
  • Neumeyer M, Brückner R: Consensus Stereostructures for the Naphthoquinonopyrano-γ-lactone Natural Products (-)-Arizonin B1 and (-)-Arizonin C1. Diastereocontrol of Oxa-Pictet-Spengler Cyclizations Eur J Org Chem, 2017; 2017: 2512-2539.
  • Neumeyer M, Kopp J, Brückner R: Controlling the Substitution Pattern of Hexasubstituted Naphthalenes by Aryne/Siloxyfuran Diels-Alder Additions: Regio- and Stereocontrolled Synthesis of Arizonin C1 Analogs Eur J Org Chem, 2017; 2017: 2883-2915.
  • Peter D, Brückner R: A New Approach to Models of the 4,5-Dihydroxycyclopentenone Core of the Kodaistatins A-D. Elucidation of the Diol Configuration in Kodaistatin A Chem-eur J, 2017; 23: 12104-12109.
  • Ruppenthal S, Brückner R: Prochiral Diheteroaryl Sulfoxides and Their Reactions With (S)-Li2-BINOLate-Activated Diisobutylmagnesium Eur J Org Chem, 2017; 2017. : http://10.1002/ejoc.201701309 (in Druck)
Buchbeiträge:
  • Hofferberth M L, Brückner R: The Tetramic Acid Antibiotics a- and b-Lipomycin: Total Synthesis and Assignment of the Absolute Configuration of all Stereogenic Centers. Making Doubly Sure In: Harmata M (Hrsg.): Strategies and Tactics in Organic Synthesis, Bd. 12 Amsterdam: Elsevier / Academic Press, 2017; 37-93 (Bd. 12).

Besondere wissenschaftliche Aktivitäten

Abschlussarbeiten