1973
DOI: 10.1016/s0040-4039(01)96069-1
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Untersuchungen über gespannte cyclische acetylene, VI Nachweis des 1,1-dimethylsila-4-cycloheptins

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Cited by 11 publications
(4 citation statements)
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“…There are not many literature reports available describing the synthesis of silacycloheptyne derivatives . A thermal generation of 1,1-dimethylsilacyclohept-4-yne and its in situ trapping by cyclopenta-2,4-dienone was reported in the 1970s, and the authors mentioned that the compound is fairly stable in diluted dichloromethane solutions (∼100 h). The atomic radius of silicon is only slightly smaller than that of selenium, and thus, the ring strain in 3 is expected to be similar to that in 10 but certainly higher than that of eight-membered dibenzocyclooctyne.…”
mentioning
confidence: 99%
“…There are not many literature reports available describing the synthesis of silacycloheptyne derivatives . A thermal generation of 1,1-dimethylsilacyclohept-4-yne and its in situ trapping by cyclopenta-2,4-dienone was reported in the 1970s, and the authors mentioned that the compound is fairly stable in diluted dichloromethane solutions (∼100 h). The atomic radius of silicon is only slightly smaller than that of selenium, and thus, the ring strain in 3 is expected to be similar to that in 10 but certainly higher than that of eight-membered dibenzocyclooctyne.…”
mentioning
confidence: 99%
“…10 Examples of silacycloheptynes with a single CH 2 for SiMe 2 substitution have been reported by Krebs, although the products were not isolable and characterized as their trapped products. 12,13 The distortion of the acetylene bond angle away from linearity (1801), as found by X-ray crystallography, is known as angle strain. 14 Chart 1 summarizes bond angles in known silacycloalkynes, with smaller ring sizes resulting in greater distortion.…”
mentioning
confidence: 99%
“…10 Examples of sila-cycloheptynes with a single CH 2 for SiMe 2 substitution have been reported by Krebs, although the products were not isolable and characterized as their trapped products. 12,13…”
mentioning
confidence: 99%
“…cm) mit Petrolether (40-70"C)/Diethylether (1 : 1) chromatographiert. Als erste Fraktion eluiert man 5,6,7, [3,2-d]pyrazol(32), ein schwach gelbliches 61; Ausb. 48 mg…”
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