Synthesis of functionalized Naphthalenes by photochemical [4 plus 2] cyclo addition between aryl acetylenic ketones and acetylenes

• Applicant: Professor Dr. Pablo Wessig
• Subject Area: Organic Molecular Chemistry - Synthesis and Characterisation
• Term: from 2003 to 2009
• Project identifier: Deutsche Forschungsgemeinschaft (DFG) - Project number 5392849

• Final Report Year: 2009

Final Report Abstract

No abstract available

Publications

• Synthesis 2005, 1445. „The Photo Dehydro Diels-Alder Reaction - An Efficient Route to Naphthalenes"
  P. Wessig, G. Müller, A. Kühn, R. Herre, H. Blumenthal, S. Troelenberg
  
• Anal. Sci. 2006, x267 „Synthesis and Crystal Structureof 11,12,23,24-tetradehydro-5,6,9,10,17,18,21,22- octahydro-7H, 19H-dibenzo[e,o][1,11 ]dioxacycloeicosin-7,19-dione"
  P. Wessig, C. Pick, B. Ziemer
  
• Chem. Comm. 2006, 4524, „Synthesis of 1,1'-Binaphthyls by Photo-Dehydro-Diels-Alder reaction"
  P. Wessig, G. Müller
  
• Helv. Chim. Acta 2006, 89, 2694, „Synthesis of Benzo[g]isochromenes through Photo-Dehydro-Diels-Alder Reaction"
  P. Wessig, G. Müller, R. Herre, A. Kühn
  
• Synthesis 2007, 464, „The Photo-Dehydro-Diels-Alder (PDDA) Reaction - A powerful method for the preparation of Biaryls"
  P. Wessig, G. Müller, C. Pick, A. Matthes
  
• Chem. Rev. 2008, 108, 205, "The Dehydro-Diels-Alder-Reaction"
  P. Wessig, G. Müller