THE ISOLATION OF EPISULFONES FROM THE RAMBERG-BACKLUND REARRANGEMENT .3.

R A  EWIN; W A  LOUGHLIN; S M  PYKE; J C  MORALES; R J K  TAYLOR

THE ISOLATION OF EPISULFONES FROM THE RAMBERG-BACKLUND REARRANGEMENT .3.

R A EWIN, W A LOUGHLIN, S M PYKE, J C MORALES, R J K TAYLOR

Chemistry

Research output: Contribution to journal › Comment/debate › peer-review

Abstract

Information on the scope and limitations of the ''Ramberg-Backlund'' approach to episulfone synthesis is provided. Several alpha-halothiane 1,1-dioxides have been converted into the corresponding isolable episulphones, but attempts to extend this procedure to related alpha-halo-thiepane, thiolane and thietane dioxides were unsuccessful. The first example of an acyclic episulphone to be prepared by the Ramberg-Backlund route is described.

Original language	English
Pages (from-to)	660-662
Number of pages	3
Journal	Synlett
Issue number	9
Publication status	Published - Sept 1993

Cite this

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title = "THE ISOLATION OF EPISULFONES FROM THE RAMBERG-BACKLUND REARRANGEMENT .3.",

abstract = "Information on the scope and limitations of the ''Ramberg-Backlund'' approach to episulfone synthesis is provided. Several alpha-halothiane 1,1-dioxides have been converted into the corresponding isolable episulphones, but attempts to extend this procedure to related alpha-halo-thiepane, thiolane and thietane dioxides were unsuccessful. The first example of an acyclic episulphone to be prepared by the Ramberg-Backlund route is described.",

author = "EWIN, {R A} and LOUGHLIN, {W A} and PYKE, {S M} and MORALES, {J C} and TAYLOR, {R J K}",

year = "1993",

month = sep,

language = "English",

pages = "660--662",

journal = "Synlett",

issn = "1437-2096",

publisher = "Georg Thieme Verlag",

number = "9",

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T1 - THE ISOLATION OF EPISULFONES FROM THE RAMBERG-BACKLUND REARRANGEMENT .3.

AU - EWIN, R A

AU - LOUGHLIN, W A

AU - PYKE, S M

AU - MORALES, J C

AU - TAYLOR, R J K

PY - 1993/9

Y1 - 1993/9

N2 - Information on the scope and limitations of the ''Ramberg-Backlund'' approach to episulfone synthesis is provided. Several alpha-halothiane 1,1-dioxides have been converted into the corresponding isolable episulphones, but attempts to extend this procedure to related alpha-halo-thiepane, thiolane and thietane dioxides were unsuccessful. The first example of an acyclic episulphone to be prepared by the Ramberg-Backlund route is described.

AB - Information on the scope and limitations of the ''Ramberg-Backlund'' approach to episulfone synthesis is provided. Several alpha-halothiane 1,1-dioxides have been converted into the corresponding isolable episulphones, but attempts to extend this procedure to related alpha-halo-thiepane, thiolane and thietane dioxides were unsuccessful. The first example of an acyclic episulphone to be prepared by the Ramberg-Backlund route is described.

M3 - Comment/debate

SN - 1437-2096

SP - 660

EP - 662

JO - Synlett

JF - Synlett

IS - 9

ER -