1993
DOI: 10.1055/s-1993-25901
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An Improved Synthesis of Cyclic Dialkynes

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1993
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Cited by 27 publications
(21 citation statements)
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“…The reactions were studied on the example of symmetrical cyclic diynes, cyclododeca 1,7 diyne (1a), cyclotetradeca 1,8 diyne (1b), and cyclohexadeca 1,9 diyne (1c). 23 Herein, based on the results obtained previously on cycloalumination of disubstituted acetylenes, 3 we devel oped conditions (cycloalkadiyne : Et 3 Al : [Zr] = 1 : 6 : 0.1, 20-22 °C, hexane, 6 h) for cycloalumination of cyclotet radeca 1,8 diyne (1b) as a model compound. Under these conditions, 1b underwent cycloalumination involving both triple bonds to give isomeric tricyclic bisaluminacyclo pentenes 2b and 3b in the ratio of 1 : 1 in 91% total yield (Scheme 2).…”
Section: Methodsmentioning
confidence: 99%
“…The reactions were studied on the example of symmetrical cyclic diynes, cyclododeca 1,7 diyne (1a), cyclotetradeca 1,8 diyne (1b), and cyclohexadeca 1,9 diyne (1c). 23 Herein, based on the results obtained previously on cycloalumination of disubstituted acetylenes, 3 we devel oped conditions (cycloalkadiyne : Et 3 Al : [Zr] = 1 : 6 : 0.1, 20-22 °C, hexane, 6 h) for cycloalumination of cyclotet radeca 1,8 diyne (1b) as a model compound. Under these conditions, 1b underwent cycloalumination involving both triple bonds to give isomeric tricyclic bisaluminacyclo pentenes 2b and 3b in the ratio of 1 : 1 in 91% total yield (Scheme 2).…”
Section: Methodsmentioning
confidence: 99%
“…The starting materials were prepared according to literature methods. [21] If not otherwise noted, the products were diastereomeric mixtures of the tricyclic diones.…”
Section: Methodsmentioning
confidence: 99%
“…Cyclotetradeca-1,8-diene (C 14 H 20 ) [11], Os 3 (CO) 10 (NCMe) 2 [12], Os 3 (CO) 10 (C 14 H 20 ) (1) [5], Os 3 (CO) 9 (C 28 H 40 ) (2) [5], and Os 3 (CO) 8 (C 14 H 20 ) 2 (3) [6] were prepared by literature methods. Co 2 (CO) 8 (from Strem) was used as received.…”
Section: Methodsmentioning
confidence: 99%