Samarium (II) iodide mediated transformations of carbohydrate derived iodo oxime ethers into stereodefined alkoxy aminocyclopentanes

J. J. Cronjé Grové; Cedric W. Holzapfel

doi:10.1016/S0040-4039(97)01748-6

Samarium (II) iodide mediated transformations of carbohydrate derived iodo oxime ethers into stereodefined alkoxy aminocyclopentanes

J. J. Cronjé Grové, Cedric W. Holzapfel

Chemical Sciences

University of Johannesburg

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

19 Citations (Scopus)

Abstract

Carbohydrate derivatives were employed as precursors in the synthesis of stereodefined alkoxy aminocyclopentanes. This rapid samarium diiodide promoted conversion involves intramolecular trapping of a radical by an oxime ether.

Original language	English
Pages (from-to)	7429-7432
Number of pages	4
Journal	Tetrahedron Letters
Volume	38
Issue number	42
DOIs	https://doi.org/10.1016/S0040-4039(97)01748-6
Publication status	Published - 20 Oct 1997

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(97)01748-6

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@article{e75826e3d8ba46a18b2432a1b76ac054,

title = "Samarium (II) iodide mediated transformations of carbohydrate derived iodo oxime ethers into stereodefined alkoxy aminocyclopentanes",

abstract = "Carbohydrate derivatives were employed as precursors in the synthesis of stereodefined alkoxy aminocyclopentanes. This rapid samarium diiodide promoted conversion involves intramolecular trapping of a radical by an oxime ether.",

author = "\{Cronj{\'e} Grov{\'e}\}, \{J. J.\} and Holzapfel, \{Cedric W.\}",

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AU - Cronjé Grové, J. J.

AU - Holzapfel, Cedric W.

PY - 1997/10/20

Y1 - 1997/10/20

N2 - Carbohydrate derivatives were employed as precursors in the synthesis of stereodefined alkoxy aminocyclopentanes. This rapid samarium diiodide promoted conversion involves intramolecular trapping of a radical by an oxime ether.

AB - Carbohydrate derivatives were employed as precursors in the synthesis of stereodefined alkoxy aminocyclopentanes. This rapid samarium diiodide promoted conversion involves intramolecular trapping of a radical by an oxime ether.

UR - https://www.scopus.com/pages/publications/0030880869

U2 - 10.1016/S0040-4039(97)01748-6

DO - 10.1016/S0040-4039(97)01748-6

M3 - Article

AN - SCOPUS:0030880869

SN - 0040-4039

VL - 38

SP - 7429

EP - 7432

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 42

ER -

Samarium (II) iodide mediated transformations of carbohydrate derived iodo oxime ethers into stereodefined alkoxy aminocyclopentanes

Abstract

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