About the mechanism of the rearrangement of β-hydroxyalkylselenides to ketones

A. Krief; J.L. Laboureur; G. Evrard; B. Norberg; E. Guittet

About the mechanism of the rearrangement of β-hydroxyalkylselenides to ketones

A. Krief, J.L. Laboureur, G. Evrard, B. Norberg, E. Guittet

Unit of theoretical and structural physico-chemistry

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

Abstract

The regio and stereochemistry of the ring enlargement of β-hydroxyalkyl methylselenides derived from cyclic ketones is disclosed and sheds some light on the intimate mechanism of the rearrangement.

Original language	English
Pages (from-to)	575-576
Number of pages	2
Journal	Tetrahedron Letters
Volume	30
Issue number	5
Publication status	Published - 1 Jan 1989

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title = "About the mechanism of the rearrangement of β-hydroxyalkylselenides to ketones",

abstract = "The regio and stereochemistry of the ring enlargement of β-hydroxyalkyl methylselenides derived from cyclic ketones is disclosed and sheds some light on the intimate mechanism of the rearrangement.",

author = "A. Krief and J.L. Laboureur and G. Evrard and B. Norberg and E. Guittet",

year = "1989",

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T1 - About the mechanism of the rearrangement of β-hydroxyalkylselenides to ketones

AU - Krief, A.

AU - Laboureur, J.L.

AU - Evrard, G.

AU - Norberg, B.

AU - Guittet, E.

PY - 1989/1/1

Y1 - 1989/1/1

N2 - The regio and stereochemistry of the ring enlargement of β-hydroxyalkyl methylselenides derived from cyclic ketones is disclosed and sheds some light on the intimate mechanism of the rearrangement.

AB - The regio and stereochemistry of the ring enlargement of β-hydroxyalkyl methylselenides derived from cyclic ketones is disclosed and sheds some light on the intimate mechanism of the rearrangement.

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M3 - Article

AN - SCOPUS:45249130517

SN - 0040-4039

VL - 30

SP - 575

EP - 576

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 5

ER -

About the mechanism of the rearrangement of β-hydroxyalkylselenides to ketones

Abstract

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