1993
DOI: 10.1021/om00033a059
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Reactions of dimethyltitanocene with alkynes and nitriles

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Cited by 67 publications
(31 citation statements)
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“…Motivated by known intermolecular reactions of the unsubstituted dimethyltitanocene with nitriles under thermal conditions [11], we made attempts to perform a controlled thermolysis of 10 in toluene-d 8 at 80 C. Unfortunately, an intractable mixture of products was observed by the NMR spectroscopy. However, methane could be identified as one of the products, indicating the expected route of thermolysis starting with CH 4 elimination.…”
Section: Reactivity Of Compounds 7 and 10mentioning
confidence: 99%
“…Motivated by known intermolecular reactions of the unsubstituted dimethyltitanocene with nitriles under thermal conditions [11], we made attempts to perform a controlled thermolysis of 10 in toluene-d 8 at 80 C. Unfortunately, an intractable mixture of products was observed by the NMR spectroscopy. However, methane could be identified as one of the products, indicating the expected route of thermolysis starting with CH 4 elimination.…”
Section: Reactivity Of Compounds 7 and 10mentioning
confidence: 99%
“…Thermolysis of Cp 2 TiMe 2 (3) at 80 °C in benzene (7 -9 h) in the presence of internal alkynes 27 forms the corresponding titanacyclobutenes 28 cleanly and efficiently (Scheme 8) [11].…”
Section: Reactions With Alkynesmentioning
confidence: 99%
“…Der hohe Elektronenbedarf des Zentralmetalls la& sich 2.B. anhand der Struktur von Titanocenamiden [CP*~T~NR'R'] ( 2 3 ) bis (25) verdeutlichen. Ohne sterische Hinderungen (R' = R' = H (2.?…”
Section: Das Prinzip Der Maximalen N-uberlappungunclassified