Original method for the ring enlargement of cyclic ketones

J.L. Laboureur; A. Krief

Original method for the ring enlargement of cyclic ketones

J.L. Laboureur, A. Krief

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

Abstract

Thallium ethoxide in chloroform was found to be a particularly valuable combination for the rearrangement of β-hydroxyselenides to ketones.

Original language	English
Pages (from-to)	2713-2716
Number of pages	4
Journal	Tetrahedron Letters
Volume	25
Issue number	25
Publication status	Published - 1 Jan 1984

Cite this

@article{fb013089c60c4f9ea4a4653d21dbb173,

title = "Original method for the ring enlargement of cyclic ketones",

abstract = "Thallium ethoxide in chloroform was found to be a particularly valuable combination for the rearrangement of β-hydroxyselenides to ketones.",

author = "J.L. Laboureur and A. Krief",

year = "1984",

month = jan,

day = "1",

language = "English",

volume = "25",

pages = "2713--2716",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier",

number = "25",

}

TY - JOUR

T1 - Original method for the ring enlargement of cyclic ketones

AU - Laboureur, J.L.

AU - Krief, A.

PY - 1984/1/1

Y1 - 1984/1/1

N2 - Thallium ethoxide in chloroform was found to be a particularly valuable combination for the rearrangement of β-hydroxyselenides to ketones.

AB - Thallium ethoxide in chloroform was found to be a particularly valuable combination for the rearrangement of β-hydroxyselenides to ketones.

UR - http://www.scopus.com/inward/record.url?scp=0001549454&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0001549454

SN - 0040-4039

VL - 25

SP - 2713

EP - 2716

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 25

ER -

Original method for the ring enlargement of cyclic ketones

Abstract

Other files and links

Fingerprint

Cite this