1986
DOI: 10.1002/ange.19860980814
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Überbrückte [14]Annulene mit Phenanthren-Perimeter:syn-1,6:7,12-Bismethano[14]annulen

Abstract: der Organolutetium-Phosphor-Bi!dungen (erstmals gemessen) betragen 2.782 und 2.813 A.[**I Diese Arbeit wurde von der Deutschen ForschungsgemeinschafI gef6r-Angew. Chem. 98 (1986) Nr. 8 0 VCH Verlagsgeselhchaft mbH. D-6940 Weinheim. 1986 0044-8249/86/08M-0729 S 02.50/0

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Cited by 15 publications
(1 citation statement)
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“…The essential value of the carbonyl coupling reaction for organic synthesis lies in the fact that intramolecular couplings of dicarbonyl compounds take place in good yields to give cycloalkenes [15]. From the numerous reported synthetic applications of this methodology only two are mentioned as examples: In the synthesis of fusicocca-2,8,10(14)-triene (7) the central eight-membered ring was closed by the reductive coupling of two aldehyde groups [16] and the cyclic 14electron .ir-system 9 was obtained from the dicarbonyl precursor 8 in 40 YO yield [17]. It should be noted that titanium-induced dicarbonyl couplings, like other cyclisation reactions to form medium and large rings, require high dilution conditions in order to realise intramolecular cyclisation rather than intermolecular polymerisation.…”
mentioning
confidence: 99%
“…The essential value of the carbonyl coupling reaction for organic synthesis lies in the fact that intramolecular couplings of dicarbonyl compounds take place in good yields to give cycloalkenes [15]. From the numerous reported synthetic applications of this methodology only two are mentioned as examples: In the synthesis of fusicocca-2,8,10(14)-triene (7) the central eight-membered ring was closed by the reductive coupling of two aldehyde groups [16] and the cyclic 14electron .ir-system 9 was obtained from the dicarbonyl precursor 8 in 40 YO yield [17]. It should be noted that titanium-induced dicarbonyl couplings, like other cyclisation reactions to form medium and large rings, require high dilution conditions in order to realise intramolecular cyclisation rather than intermolecular polymerisation.…”
mentioning
confidence: 99%