Synthesis of helicenophanes containing two carbocyclic five-membered rings

Polycyclic Aromatic Compounds

Volumn 25, Issue 1, 2005, Pages 13-22

  Minuti, Lucio ^a   Taticchi, Aldo ^a   Marrocchi, Assunta ^a   Gacs Baitz, Eszter ^b  

^a UNIVERSITY OF PERUGIA   (Italy)

^b CTRL RES INSTITUTE FOR CHEMISTRY   (Hungary)

Author keywords

Diels Alder reaction; Helicenophanes; High pressure; NMR spectroscopy

Indexed keywords

CHEMICAL REACTIONS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

CYCLOADDUCTS; DIELS-ALDER REACTION; FIVE-MEMBERED RINGS; HELICENOPHANE; HIGH PRESSURE; HIGHER YIELD; NMR-SPECTROSCOPY; SPECTROSCOPIC DATA;

KETONES;

ALKADIENE; BROMINE; CARBOXYLIC ACID DERIVATIVE; KETONE;

ANALYTIC METHOD; AROMATIZATION; ARTICLE; CHEMICAL PROCEDURES; CHEMICAL REACTION; CYCLOADDITION; DIELS ALDER REACTION; HYPERBARISM; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; REACTION ANALYSIS; SPECTROSCOPY; SYNTHESIS;

EID: 13844271122     PISSN: 10406638     EISSN: None     Source Type: Journal    
DOI: 10.1080/10406630490474525     Document Type: Article

References (9)

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2. (a) L. Minuti, A. Taticchi, C. Rosini, D. Lanari, A. Marrocchi, and S. Superchi, Synthesis and Absolute Configuration of a New Chiral [2.2]paracyclophane-Based diene, Tetrahedron: Asymmetry 13 (2002):1257-1263.
3. (b) L. Minuti, A. Taticchi, A. Marrocchi, D. Lanari, A. Broggi, and E. Gacs-Baitz, Synthesis of Enantiopure Angularly Condensed [2.2]paracyclophanes Containing Five-Membered Rings, Tetrahedron: Asymmetry 14 (2003):481-487.
4. (c) L. Minuti, A. Taticchi, A. Marrocchi, L. Costantini, and E. Gacs-Baitz, Stereoselective Synthesis of Enantiopure Condensed [2.2]paracyclophanes, Tetrahedron: Asymmetry 12 (2001):1179-1183.
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