Stereochemistry of the C addition of 1-lithio 1,1-bis methylselenoalkanes to methyl cyclohexenones

J. Lucchetti; A. Krief

Stereochemistry of the C addition of 1-lithio 1,1-bis methylselenoalkanes to methyl cyclohexenones

J. Lucchetti, A. Krief

Research output: Contribution to journal › Article › peer-review

Abstract

The presence of DME or HMPT allows the C regio and stereoselective introduction of 1,1-bis methylselenoalkanes to methyl cyclohexenones. The resulting compounds have been stereoselective transformed to 3-ethyl methyl cyclohexanones.

Original language	English
Pages (from-to)	1623-1626
Number of pages	4
Journal	Tetrahedron Letters
Volume	22
Issue number	17
Publication status	Published - 1 Jan 1981

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title = "Stereochemistry of the C addition of 1-lithio 1,1-bis methylselenoalkanes to methyl cyclohexenones",

abstract = "The presence of DME or HMPT allows the C regio and stereoselective introduction of 1,1-bis methylselenoalkanes to methyl cyclohexenones. The resulting compounds have been stereoselective transformed to 3-ethyl methyl cyclohexanones.",

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N2 - The presence of DME or HMPT allows the C regio and stereoselective introduction of 1,1-bis methylselenoalkanes to methyl cyclohexenones. The resulting compounds have been stereoselective transformed to 3-ethyl methyl cyclohexanones.

AB - The presence of DME or HMPT allows the C regio and stereoselective introduction of 1,1-bis methylselenoalkanes to methyl cyclohexenones. The resulting compounds have been stereoselective transformed to 3-ethyl methyl cyclohexanones.

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Stereochemistry of the C addition of 1-lithio 1,1-bis methylselenoalkanes to methyl cyclohexenones

Abstract

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