INTRAMOLECULAR CARBOMETALLATION OF GRIGNARD REAGENTS HAVING THE TERMINAL TRIMETHYLSILYLACETYLENE GROUP

DOI: 10.1016/S0040-4039(01)90096-6

Source and publish data:

Tetrahedron Letters p. 1999 - 2002 (1984)

Update date:2022-09-26

Topics:

Authors:

Fujikura, Sadao

Inoue, Masaharu

Utimoto, Kiitiro

Nozaki, Hitosi

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Article abstract of DOI:10.1016/S0040-4039(01)90096-6

Reaction of 6-bromo-1-trimethylsilyl-1-hexyne with magnesium affords the corresponding Grignard reagent whose C-Mg bond intramolecularly adds to the trimethylsilylacetylene moiety in 5-Exo-Dig manner and suprafacially.The reaction can be applied to the synthesis of some cycloalkanes having stereodefined alkylidene substituents.

Full text of DOI:10.1016/S0040-4039(01)90096-6

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