Thieme Chemistry Journal Awardees - Where are They Now? Synthesis of the Marine Glycolipid Dioctadecanoyl Discoside

Gordon John Florence; Tashfeen Aslam; Gavin John Miller; Gavin Douglas Stirling Milne; Stuart Conway

doi:10.1055/s-0029-1218301

Thieme Chemistry Journal Awardees - Where are They Now? Synthesis of the Marine Glycolipid Dioctadecanoyl Discoside

Gordon John Florence
, Tashfeen Aslam
, Gavin John Miller
, Gavin Douglas Stirling Milne
, Stuart Conway

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

Abstract

The first synthesis of the inositol-containing marine glycolipid dioctadecanoyl discoside is reported. The key glycosylation reaction proceeds with β-selectivity at reduced temperature. The separable anomers could be readily progressed to afford discoside, its peracetate and the unnatural β-derivatives.

Original language	English
Pages (from-to)	3099-3102
Number of pages	4
Journal	Synlett
Volume	2009
Issue number	19
Early online date	21 Oct 2009
DOIs	https://doi.org/10.1055/s-0029-1218301
Publication status	Published - 1 Dec 2009

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 14 Life Below Water

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10.1055/s-0029-1218301

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Research Grants Scheme 2007/R1: Research Grants Scheme- 2007/R1
Florence, G. (PI)
The Royal Society
1/08/07 → 31/07/08
Project: Standard
The Royal Society 516002.K501/kk: Dr G Florence research fellowship application - 2005
Florence, G. (PI)
The Royal Society
1/10/05 → 30/09/10
Project: Fellowship
BB/C515255/1: A Reverse chemical genetics and chemical biology approach to probing 1,4,5-trisphosphate receptor function
Conway, S. (PI)
Biotechnology and Biological Sciences Research Council
1/02/05 → 31/08/08
Project: Standard

Cite this

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title = "Thieme Chemistry Journal Awardees - Where are They Now? Synthesis of the Marine Glycolipid Dioctadecanoyl Discoside",

abstract = "The first synthesis of the inositol-containing marine glycolipid dioctadecanoyl discoside is reported. The key glycosylation reaction proceeds with β-selectivity at reduced temperature. The separable anomers could be readily progressed to afford discoside, its peracetate and the unnatural β-derivatives.",

author = "Florence, \{Gordon John\} and Tashfeen Aslam and Miller, \{Gavin John\} and Milne, \{Gavin Douglas Stirling\} and Stuart Conway",

year = "2009",

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doi = "10.1055/s-0029-1218301",

language = "English",

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issn = "0936-5214",

publisher = "Georg Thieme Verlag",

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AU - Florence, Gordon John

AU - Aslam, Tashfeen

AU - Miller, Gavin John

AU - Milne, Gavin Douglas Stirling

AU - Conway, Stuart

PY - 2009/12/1

Y1 - 2009/12/1

N2 - The first synthesis of the inositol-containing marine glycolipid dioctadecanoyl discoside is reported. The key glycosylation reaction proceeds with β-selectivity at reduced temperature. The separable anomers could be readily progressed to afford discoside, its peracetate and the unnatural β-derivatives.

AB - The first synthesis of the inositol-containing marine glycolipid dioctadecanoyl discoside is reported. The key glycosylation reaction proceeds with β-selectivity at reduced temperature. The separable anomers could be readily progressed to afford discoside, its peracetate and the unnatural β-derivatives.

U2 - 10.1055/s-0029-1218301

DO - 10.1055/s-0029-1218301

M3 - Letter

SN - 0936-5214

VL - 2009

SP - 3099

EP - 3102

JO - Synlett

JF - Synlett

IS - 19

ER -

Thieme Chemistry Journal Awardees - Where are They Now? Synthesis of the Marine Glycolipid Dioctadecanoyl Discoside

Abstract

UN SDGs

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Projects

Research Grants Scheme 2007/R1: Research Grants Scheme- 2007/R1

The Royal Society 516002.K501/kk: Dr G Florence research fellowship application - 2005

BB/C515255/1: A Reverse chemical genetics and chemical biology approach to probing 1,4,5-trisphosphate receptor function

Cite this