The synthesis of conformationally-restricted diacyl glycerol analogues

J C  BRIGGS; A P  DAWSON; I  GIBSON; A H  HAINES; J  HOOK; R J K  TAYLOR

doi:10.1016/S0960-894X(01)80434-0

The synthesis of conformationally-restricted diacyl glycerol analogues

J C BRIGGS, A P DAWSON, I GIBSON, A H HAINES, J HOOK, R J K TAYLOR

Chemistry

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

Abstract

A series of conformationally-restricted diacylglycerol analogues have been prepared in homochiral form as potential protein kinase C antagonists using D-ribonolactone and D- and L-2-deoxyribose as starting materials.

Original language	English
Pages (from-to)	131-134
Number of pages	4
Journal	Bioorganic & Medicinal Chemistry Letters
Volume	2
Issue number	2
DOIs	https://doi.org/10.1016/S0960-894X(01)80434-0
Publication status	Published - 1992

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10.1016/S0960-894X(01)80434-0

Cite this

@article{69401a194ec744e0aa8aeb106dcf6ba4,

title = "The synthesis of conformationally-restricted diacyl glycerol analogues",

abstract = "A series of conformationally-restricted diacylglycerol analogues have been prepared in homochiral form as potential protein kinase C antagonists using D-ribonolactone and D- and L-2-deoxyribose as starting materials.",

author = "BRIGGS, {J C} and DAWSON, {A P} and I GIBSON and HAINES, {A H} and J HOOK and TAYLOR, {R J K}",

year = "1992",

doi = "10.1016/S0960-894X(01)80434-0",

language = "English",

volume = "2",

pages = "131--134",

journal = "Bioorganic & Medicinal Chemistry Letters",

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T1 - The synthesis of conformationally-restricted diacyl glycerol analogues

AU - BRIGGS, J C

AU - DAWSON, A P

AU - GIBSON, I

AU - HAINES, A H

AU - HOOK, J

AU - TAYLOR, R J K

PY - 1992

Y1 - 1992

N2 - A series of conformationally-restricted diacylglycerol analogues have been prepared in homochiral form as potential protein kinase C antagonists using D-ribonolactone and D- and L-2-deoxyribose as starting materials.

AB - A series of conformationally-restricted diacylglycerol analogues have been prepared in homochiral form as potential protein kinase C antagonists using D-ribonolactone and D- and L-2-deoxyribose as starting materials.

U2 - 10.1016/S0960-894X(01)80434-0

DO - 10.1016/S0960-894X(01)80434-0

M3 - Article

SN - 0960-894X

VL - 2

SP - 131

EP - 134

JO - Bioorganic & Medicinal Chemistry Letters

JF - Bioorganic & Medicinal Chemistry Letters

IS - 2

ER -