Selective formation of 1,3-oxazolidine-2-thiones on ketohexose templates

A Tatibouet; S Lawrence; P Rollin; G D Holman

doi:10.1055/s-2004-830886

Selective formation of 1,3-oxazolidine-2-thiones on ketohexose templates

A Tatibouet, S Lawrence, P Rollin, G D Holman

Department of Life Sciences

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

19 Citations (SciVal)

Abstract

Thiocyanic acid condensation on selectively protected ketohexose led to the isolation of five out of the seven possible 1,3-oxazolidine-2-thiones (OZT). The four isomeric spiro-OZT synthesized showed promising biological activity against D-fructose transport.

Original language	English
Pages (from-to)	1945-1948
Number of pages	4
Journal	Synlett
Issue number	11
DOIs	https://doi.org/10.1055/s-2004-830886
Publication status	Published - 2004

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ID number: ISI:000223845200016

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10.1055/s-2004-830886

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@article{3d91dcbdd8754aaeae77e33b0c6baa01,

title = "Selective formation of 1,3-oxazolidine-2-thiones on ketohexose templates",

abstract = "Thiocyanic acid condensation on selectively protected ketohexose led to the isolation of five out of the seven possible 1,3-oxazolidine-2-thiones (OZT). The four isomeric spiro-OZT synthesized showed promising biological activity against D-fructose transport.",

author = "A Tatibouet and S Lawrence and P Rollin and Holman, \{G D\}",

note = "ID number: ISI:000223845200016",

year = "2004",

doi = "10.1055/s-2004-830886",

language = "English",

pages = "1945--1948",

journal = "Synlett",

issn = "0936-5214",

publisher = "Georg Thieme Verlag",

number = "11",

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TY - JOUR

T1 - Selective formation of 1,3-oxazolidine-2-thiones on ketohexose templates

AU - Tatibouet, A

AU - Lawrence, S

AU - Rollin, P

AU - Holman, G D

N1 - ID number: ISI:000223845200016

PY - 2004

Y1 - 2004

N2 - Thiocyanic acid condensation on selectively protected ketohexose led to the isolation of five out of the seven possible 1,3-oxazolidine-2-thiones (OZT). The four isomeric spiro-OZT synthesized showed promising biological activity against D-fructose transport.

AB - Thiocyanic acid condensation on selectively protected ketohexose led to the isolation of five out of the seven possible 1,3-oxazolidine-2-thiones (OZT). The four isomeric spiro-OZT synthesized showed promising biological activity against D-fructose transport.

UR - https://www.scopus.com/pages/publications/4544311889

U2 - 10.1055/s-2004-830886

DO - 10.1055/s-2004-830886

M3 - Article

SN - 0936-5214

SP - 1945

EP - 1948

JO - Synlett

JF - Synlett

IS - 11

ER -

Selective formation of 1,3-oxazolidine-2-thiones on ketohexose templates

Abstract

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